Chimeric Antigen Receptor T-Cell Therapy Pipeline, Clinical Trials, FDA Approvals, Research and Developments, Future Perspectives, and Companies (Updated)

DelveInsight’s, “CAR-T Therapy Pipeline Insight 2023” report provides comprehensive insights about 200+ CAR-T Therapy companies and 252+ pipeline drugs in the CAR-T Therapy pipeline landscape. It covers the CAR-T Therapy pipeline drug profiles, including clinical and nonclinical stage products. It also covers the CAR-T Therapy pipeline therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

 

Key Takeaways from the CAR-T Therapy Pipeline Report

  • DelveInsight’s CAR-T Therapy pipeline report depicts a robust space with 200+ active players working to develop 252+ pipeline therapies for CAR-T Therapy treatment.
  • The leading CAR-T Therapy companies working in the market include CARsgen, CASI Pharmaceuticals, Tessa Therapeutics, Cartesian Therapeutics, Gracell Bio, Aurora BioPharma, Carsgen Therapeutics, Autolus Limited, CRISPR Therapeutics, Allogene Therapeutics, Verismo Therapeutics, Arcellx, Nexcella, JW Therapeutics, Janssen Pharmaceuticals, Chongqing Precision Biotech, CoImmune, Inc., Mustang Bio, Novartis Pharmaceuticals, Shanghai Unicar-Therapy Bio-medicine Technology, Sotio Biotech Inc., Beam Therapeutics, AbCLon, Nanjing IASO Biotherapeutics, Autolus, Beijing Immunochina Medical Science and Technology, Carsgen Therapeutics, Orgenesis, IN8Bio, Oxford BioMedica, and others.
  • Promising CAR-T Therapy Pipeline Therapies in the various stages of development include Glofitamab, Obinutuzumab, Tocilizumab, Pembrolizumab, C-CAR066, Mosunetuzumab, Polatuzumab, and others.
  • January 2024: Janssen Research & Development LLC announced a study of Phase 2 clinical trials for JNJ-68284528, Lenalidomide, Daratumumab, Bortezomib and Dexamethasone. The purpose of this study is to evaluate the overall minimal residual disease (MRD) negative rate of participants who receive JNJ-68284528.
  • January 2024: CARsgen Therapeutics Co. Ltdannounced a study of Phase 1 & 2 clinical trials for CT041 autologous CAR T-cell injection. This study is an open, multicenter, Phase Ib/II clinical trial evaluating chimeric antigen receptor-modified autologous T cells targeting Claudin18.2 (CLDN18.2) (CT041 autologous CAR T) in subjects with CLDN18.2 expression-positive, advanced gastric/esophagogastric conjugate adenocarcinoma that has failed at least 2 prior lines therapy and advanced pancreatic cancer that has failed at least 1 prior line therapy. The purpose is to evaluate the efficacy, safety and pharmacokinetics There are two stages in the study. Phase Ib stage is dose escalation and dose expansion study, and Phase II stage is to verify the efficacy and safety of CT041 treatment.
  • January 2024: Caribou Biosciences Inc. announced a study of Phase 1 clinical trials for CB-011. This is a Phase 1 study to evaluate the safety of CB-011 (the study treatment), an allogeneic chimeric antigen receptor (CAR-T) cell therapy that targets the B cell maturation antigen (BCMA), to determine the best dose of CB-011, and to assess the effectiveness of CB-011 in treating multiple myeloma that has come back (relapsed) or that is no longer responding to other treatment (refractory).
  • December 2023: Novartis Pharmaceuticals announced a study of Phase 2 clinical trials for PHE885. A Phase 2 Study of PHE885, B-cell Maturation Antigen (BCMA)- Directed CAR-T Cells in Adult Participants With Relapsed and Refractory Multiple Myeloma.
  • December 2023: Allogene Therapeutics announced a study of Phase 1 clinical trials for ALLO-501, ALLO-647, Fludarabine and Cyclophosphamide. The purpose of the ALPHA study is to assess the safety, efficacy, cell kinetics and immunogenicity of ALLO-501 in adults with relapsed or refractory large B-cell lymphoma or follicular lymphoma after a lymphodepletion regimen comprising fludarabine, cyclophosphamide, and ALLO-647.

 

Request a sample and discover the recent advances in CAR-T Therapy Drugs @ CAR-T Therapy Pipeline Outlook Report

 

In the CAR-T Therapy Pipeline Report, detailed description of the drug is given which includes mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, CAR-T Therapy collaborations, licensing, mergers and acquisition, funding, designations and other product related details. The assessment part of the report embraces, in depth CAR-T Therapy commercial assessment and clinical assessment of the CAR-T Therapy pipeline products under development.

 

CAR-T Therapy Overview

CAR T cell therapy uses T cells engineered with CARs to treat cancer. The premise of CAR T immunotherapy is to modify T cells to recognize cancer cells to more effectively target and destroy them. Scientists harvest T cells from people, genetically alter them, and then infuse the resulting CAR T cells into patients to attack their tumors. Cancer Immunotherapy utilizes and enhances the immune system’s standard capacity and is considered one of the most promising approaches for treating various diseases (including cancer, autoimmune diseases, and allergic–hypersensitivity reactions) are severe.

 

Find out more about CAR-T Therapy Analysis @ CAR-T Therapy Drugs

 

CAR-T Therapy Emerging Drugs Profile

  • CT053: Carsgen Therapeutics
  • Descartes-08: Cartesian Therapeutics
  • ALLO-501A: Allogene Therapeutics
  • CTX110: CRISPR Therapeutics
  • IMPT 314: ImmPACT Bio
  • ALLO-715: Allogene Therapeutics

 

CAR-T Therapy Therapeutics Assessment

There are approx. 200+ CAR-T Therapy companies which are developing the therapies for CAR-T Therapy. The CAR-T Therapy companies which have their CAR-T Therapy drug candidates in the most advanced stage, i.e. Registered include, Carsgen Therapeutics. The CAR-T Therapy pipeline report proffers an integral view of the emerging CAR-T Therapy segmented by stage, product type, molecule type, and route of administration.

 

CAR-T Therapy pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as

  • Oral
  • Intravenous
  • Subcutaneous
  • Parenteral
  • Topical

 

Dive deep into rich insights for new CAR-T Therapy, visit @ CAR-T Therapy Treatment Landscape

 

CAR-T Therapy Products have been categorized under various Molecule types such as

  • Recombinant fusion proteins
  • Small molecule
  • Monoclonal antibody
  • Peptide
  • Polymer
  • Gene therapy

 

Scope of the CAR-T Therapy Pipeline Report

  • Coverage- Global
  • CAR-T Therapy Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
  • CAR-T Therapy Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III
  • CAR-T Therapy Companies- CARsgen, CASI Pharmaceuticals, Tessa Therapeutics, Cartesian Therapeutics, Gracell Bio, Aurora BioPharma, Carsgen Therapeutics, Autolus Limited, CRISPR Therapeutics, Allogene Therapeutics, Verismo Therapeutics, Arcellx, Nexcella, JW Therapeutics, Janssen Pharmaceuticals, Chongqing Precision Biotech, CoImmune, Inc., Mustang Bio, Novartis Pharmaceuticals, Shanghai Unicar-Therapy Bio-medicine Technology, Sotio Biotech Inc., Beam Therapeutics, AbCLon, Nanjing IASO Biotherapeutics, Autolus, Beijing Immunochina Medical Science and Technology, Carsgen Therapeutics, Orgenesis, IN8Bio, Oxford BioMedica, and others.
  • CAR-T Therapy Pipeline Therapies- Glofitamab, Obinutuzumab, Tocilizumab, Pembrolizumab, C-CAR066, Mosunetuzumab, Polatuzumab, and others.

 

For further information on the CAR-T Therapy Pipeline Therapeutics, reach out @ CAR-T Therapy Therapeutics Segmentation

 

Table of Content

  1. Introduction
  2. Executive Summary
  3. CAR-T Therapy: Overview
  4. Pipeline Therapeutics
  5. Therapeutic Assessment
  6. CAR-T Therapy– DelveInsight’s Analytical Perspective
  7. Late Stage Products (Registered)
  8. CT053: Carsgen Therapeutics
  9. Drug profiles in the detailed report…..
  10. Mid Stage Products (Phase II)
  11. Descartes-08: Cartesian Therapeutics
  12. Drug profiles in the detailed report…..
  13. Early Stage Products (Phase I)
  14. ALLO-715: Allogene Therapeutics
  15. Drug profiles in the detailed report…..
  16. Preclinical and Discovery Stage Products
  17. ACLX 003: Arcellx
  18. Drug profiles in the detailed report…..
  19. Inactive Products
  20. CAR-T Therapy Key Companies
  21. CAR-T Therapy Key Products
  22. CAR-T Therapy- Unmet Needs
  23. CAR-T Therapy- Market Drivers and Barriers
  24. CAR-T Therapy- Future Perspectives and Conclusion
  25. CAR-T Therapy Analyst Views
  26. CAR-T Therapy Key Companies
  27. Appendix

 

Find out more about CAR-T Therapy Therapeutics Assessment @ CAR-T Therapy Preclinical and Discovery Stage Products

  

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Yash Bhardwaj
Email: Send Email
Phone: 9650213330
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: Nevada
Country: United States
Website: https://www.delveinsight.com/report-store/mouth-neoplasms-market

 

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To view the original version on ABNewswire visit: Chimeric Antigen Receptor T-Cell Therapy Pipeline, Clinical Trials, FDA Approvals, Research and Developments, Future Perspectives, and Companies (Updated)

Glioma Pipeline, Clinical Trials, FDA Approvals, Research and Developments, Future Perspectives, and Companies (Updated)

DelveInsight’s, “Glioma Pipeline Insight 2023” report provides comprehensive insights about 200+ Glioma companies and 220+ pipeline drugs in the Glioma pipeline landscape. It covers the Glioma pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Glioma therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

 

Key Takeaways from the Glioma Pipeline Report

  • DelveInsight’s Glioma pipeline report depicts a robust space with 200+ active players working to develop 220+ pipeline therapies for Glioma treatment.
  • The leading Glioma companies working in the market include Denovo Biopharma, AstraZeneca, Pfizer, Chimerix, Bristol-Myers Squibb, Orbus Therapeutics, Northwest Biotherapeutics, Day One Biopharmaceuticals, AiVita Biomedical, Ascletis Pharma Inc., Bristol Myers Squibb, Kazia Therapeutics, HebaBiz Biotech, Biohaven Pharmaceuticals, Vigeo Therapeutics, Hoffman-La-Roche, TVAX Biomedical, Laminar Pharmaceuticals, Kintara Therapeutics, Medicenna Therapeutics, Symphogen A/S, MimiVax, Incyte Corporation, Istari Oncology, Immunomic Therapeutics, Celgene, Sanofi, Merck Sharp & Dohme LLC, Oblato Inc., GlaxoSmithKline, NuvOx Pharma, Epitopoietic Research Corporation, AnHeart Therapeutics, DNAtrix, Arog Pharmaceuticals, CANbridge Pharmaceuticals, Jiangsu Hengrui Medicine, BPGbio Inc., BioMimetix, CNS Pharmaceuticals, and others.
  • Promising Glioma Pipeline Therapies in the various stages of development include DS-1001b, Nimotuzumab, Radiotherapy, AP23573, BLZ-100, LY2157299, Temozolomide, Safusidenib, ONC201, PLB1001, YYB-103, and others.
  • December 2023: Day One Biopharmaceuticals Inc. announced a study of Phase 3 clinical trials for DAY101 and Chemotherapeutic Agent. This is a 2-arm, randomized, open-label, multicenter, global, Phase 3 trial to evaluate the efficacy, safety, and tolerability of DAY101 monotherapy versus standard of care (SoC) chemotherapy in patients with pediatric low-grade glioma (LGG) harboring an activating rapidly accelerated fibrosarcoma (RAF) alteration requiring front-line systemic therapy.
  • December 2023: Daiichi Sankyo Co. Ltd announced a study of Phase 2 clinical trials for DS-1001b. This Phase 2 study is conducted to assess the efficacy and safety of DS-1001b in patients with chemotherapy- and radiotherapy-naive IDH1 mutated WHO grade II glioma.
  • December 2023: Chimerixannounced a study of Phase 3 clinical trials for ONC201. This is a randomized, double-blind, placebo-controlled, parallel-group, international, Phase 3 study in patients with newly diagnosed H3 K27M-mutant diffuse glioma to assess whether treatment with ONC201 following frontline radiotherapy will extend overall survival and progression-free survival in this population. Eligible participants will have histologically diagnosed H3 K27M-mutant diffuse glioma and have completed standard frontline radiotherapy.
  • December 2023: Aveta Biomics Inc. announced a study of Phase 1 & 2 clinical trials for APG-157. The goal of this interventional study is to evaluate the efficacy of APG-157 in combination with Bevacizumab in subjects with recurrent high-grade glioma who have previously progressed on bevacizumab alone.
  • December 2023: Boehringer Ingelheimannounced a study of Phase 1 clinical trials for BI 764532. The purpose of this study is to find out the highest dose of BI 764532 that people with a brain tumour that is positive for DLL3 can tolerate. BI 764532 is an antibody-like molecule that can attach and link together the cancer cells and T-cells of the immune system (DLL3/CD3 bispecific). This may help the immune system fight cancer.

 

Request a sample and discover the recent advances in Glioma Drugs @ Glioma Pipeline Outlook Report

 

In the Glioma Pipeline Report, detailed description of the drug is given which includes mechanism of action of the drug, Glioma clinical trials studies, NDA approvals (if any), and product development activities comprising the technology, Glioma collaborations, licensing, mergers and acquisition, funding, designations and other product related details. The assessment part of the report embraces, in depth Glioma commercial assessment and clinical assessment of the Glioma pipeline products under development.

 

Glioma Overview

A glioma is a tumor that forms in the brain or spinal cord. Neuroglial cells also known as glial cells or glia are quite different from nerve cells. They do not participate directly in synaptic interactions and electrical signaling, although their supportive functions help define synaptic contacts and maintain the signaling abilities of neurons. Glia are more numerous than nerve cells in the brain, outnumbering them by a ratio of perhaps 3 to 1. Although glial cells also have complex processes extending from their cell bodies, they are generally smaller than neurons, and they lack axons and dendrites.

 

Find out more about Glioma Analysis @ Glioma Drugs

 

Glioma Emerging Drugs Profile

  • Tofacitinib: Pfizer
  • Enzastaurin: Denovo BioPharma
  • MDNA55: Medicenna Therapeutics, Inc.
  • Sym004: Symphogen A/S
  • MN-166: MediciNova

 

Glioma Therapeutics Assessment

There are approx. 200+ Glioma companies which are developing the therapies for Glioma Disease. The Glioma companies which have their Glioma Disease drug candidates in the most advanced stage, i.e. Phase III include, Denovo BioPharma. The Glioma pipeline report proffers an integral view of the emerging Glioma segmented by stage, product type, molecule type, and route of administration.

 

Glioma Disease pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as

  • Intravenous
  • Subcutaneous
  • Oral
  • Intramuscular

 

Dive deep into rich insights for new Glioma, visit @ Glioma Treatment Landscape

 

Glioma Products have been categorized under various Molecule types such as

  • Monoclonal antibody
  • Small molecule
  • Peptide

 

Scope of the Glioma Pipeline Report

  • Coverage- Global
  • Glioma Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
  • Glioma Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III
  • Glioma Companies- Denovo Biopharma, AstraZeneca, Pfizer, Chimerix, Bristol-Myers Squibb, Orbus Therapeutics, Northwest Biotherapeutics, Day One Biopharmaceuticals, AiVita Biomedical, Ascletis Pharma Inc., Bristol Myers Squibb, Kazia Therapeutics, HebaBiz Biotech, Biohaven Pharmaceuticals, Vigeo Therapeutics, Hoffman-La-Roche, TVAX Biomedical, Laminar Pharmaceuticals, Kintara Therapeutics, Medicenna Therapeutics, Symphogen A/S, MimiVax, Incyte Corporation, Istari Oncology, Immunomic Therapeutics, Celgene, Sanofi, Merck Sharp & Dohme LLC, Oblato Inc., GlaxoSmithKline, NuvOx Pharma, Epitopoietic Research Corporation, AnHeart Therapeutics, DNAtrix, Arog Pharmaceuticals, CANbridge Pharmaceuticals, Jiangsu Hengrui Medicine, BPGbio Inc., BioMimetix, CNS Pharmaceuticals, and others.
  • Glioma Therapies- DS-1001b, Nimotuzumab, Radiotherapy, AP23573, BLZ-100, LY2157299, Temozolomide, Safusidenib, ONC201, PLB1001, YYB-103, and others.

 

For further information on the Glioma Pipeline Therapeutics, reach out @ Glioma Therapeutics Segmentation

 

Table of Content

  1. Introduction
  2. Executive Summary
  3. Glioma Disease: Overview
  4. Glioma Pipeline Therapeutics
  5. Glioma Therapeutic Assessment
  6. Glioma Disease– DelveInsight’s Analytical Perspective
  7. Late Stage Products (Phase III)
  8. Enzastaurin: Denovo BioPharma
  9. Drug profiles in the detailed report…..
  10. Mid Stage Products (Phase II)
  11. MDNA55: Medicenna Therapeutics, Inc.
  12. Drug profiles in the detailed report…..
  13. Early Stage Products (Phase I/II)
  14. Zotiraciclib: Adastra Pharmaceuticals
  15. Drug profiles in the detailed report…..
  16. Preclinical and Discovery Stage Products
  17. RGN6024: Reglagene, Inc.
  18. Drug profiles in the detailed report…..
  19. Inactive Products
  20. Glioma Disease Key Companies
  21. Glioma Disease Key Products
  22. Glioma Disease- Unmet Needs
  23. Glioma Disease- Market Drivers and Barriers
  24. Glioma Disease- Future Perspectives and Conclusion
  25. Glioma Disease Analyst Views
  26. Glioma Disease Key Companies
  27. Appendix

 

Find out more about Glioma Therapeutics Assessment @ Glioma Preclinical and Discovery Stage Products

 

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Yash Bhardwaj
Email: Send Email
Phone: 9650213330
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: Nevada
Country: United States
Website: https://www.delveinsight.com/report-store/mouth-neoplasms-market

 

Press Release Distributed by ABNewswire.com

To view the original version on ABNewswire visit: Glioma Pipeline, Clinical Trials, FDA Approvals, Research and Developments, Future Perspectives, and Companies (Updated)

Gastric Cancer Pipeline, Clinical Trials, FDA Approvals, Research and Developments, Future Perspectives, and Companies (Updated)

DelveInsight’s, “Gastric Cancer Pipeline Insight 2023” report provides comprehensive insights about 180+ Gastric Cancer companies and 200+ pipeline drugs in the Gastric Cancer pipeline landscape. It covers the Gastric Cancer pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Gastric Cancer therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

 

Key Takeaways from the Gastric Cancer Pipeline Report

  • DelveInsight’s Gastric Cancer pipeline report depicts a robust space with 180+ companies working to develop 200+ pipeline Gastric Cancer.
  • The leading Gastric Cancer companies working in the market include Linton Pharm Co.Ltd., Shanghai Henlius Biotech, RAPT Therapeutics, AstraZeneca, Astellas Pharma, Minneamrita Therapeutics, Aston Science, Servier Bio-Innovation LLC, Bukwang Pharmaceutical, TaihoOncology Inc., Novartis Pharmaceuticals, Base Therapeutics (Shanghai) Co. Ltd, Shanghai MiracogenInc., RemeGen Co Ltd., Idience Co. Ltd., BeiGene, Ono Pharmaceutical Co. Ltd, Elevar Therapeutics, R-Pharm, Innovent Biologics (Suzhou) Co.Ltd., Macro Genics, Sichuan Baili Pharmaceutical Co. Ltd., LianBio LLC, Janssen Pharmaceutical, and others.
  • Promising Gastric Cancer Pipeline Therapies in the various stages of development include S-1/Cisplatin, FLX475, Pembrolizumab, Tegafur-gimeracil-oteracil potassium, Oxaliplatin, Volitinib, Docetaxel, and others.
  • December 2023: Hanmi Pharmaceutical Company Limited announced a study of Phase 2 clinical trials for Pembrolizumab and FLX475. This clinical study is a Phase 2, open-label study to assess the efficacy, safety profile of FLX475 combined with pembrolizumab in patients with advanced or metastatic gastric cancer. This study is designed to assess the potential anti-tumor activity when administered at the 100mg QD of FLX475 with pembrolizumab and will be conducted (2) cohorts.
  • December 2023: Ono Pharmaceuticals Co. Ltd, announced a study of Phase 3 clinical trials for Nivolumab, Oxaliplatin and Capecitabine. The purpose of study is to evaluate the efficacy and safety of postoperative adjuvant chemotherapy with Nivolumab in combination with tegafur-gimeracil-oteracil potassium (S-1 therapy) or capecitabine + oxaliplatin (CapeOX therapy), in comparison with placebo in combination with S-1 therapy or CapeOX therapy, in pStage III gastric cancer (including esophagogastric junction cancer) after D2 or more extensive lymph node dissection.
  • December 2023: RemeGen Co. Ltd announced a study of Phase 3 clinical trials for RC48-ADC and Apatinib Mesylate Tablets. This is a Phase III, randomized, multicenter, open-label clinical trial designed to compare RC48-ADC to physician choice standard treatment in participants with human epidermal growth factor receptor 2 (HER2)-overexpression locally advanced or metastatic gastric cancer.
  • December 2023: Merck Sharp & Dohme LLC announced a study of Phase 2 clinical trials for Pembrolizumab, Oxaliplatin, and Cisplatin. The purpose of this study is to estimate objective response rates (ORRs) of pembrolizumab + oxaliplatin + TS-1 and pembrolizumab + cisplatin + TS-1, as first-line treatment for gastric cancer in programmed death-ligand 1 (PD-L1) positive, human epidermal growth factor receptor 2 (HER2/neu)-negative participants with advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma.
  • December 2023: Sanofi announced a study of Phase 3 clinical trials for Docetaxel (XRP6976) and Oxaliplatin (SR96669). Participants in the neoadjuvant chemotherapy arm were treated for 3 cycles (1 cycle is 21 days) before surgery and treated for a year with S-1. Participants in the adjuvant chemotherapy arm underwent surgery and were treated for a year with S-1.

 

Request a sample and discover the recent advances in Gastric Cancer Drugs @ Gastric Cancer Pipeline Outlook Report

 

In the Gastric Cancer Pipeline Report, detailed description of the drug is given which includes mechanism of action of the drug, Gastric Cancer clinical trials studies, NDA approvals (if any), and product development activities comprising the technology, Gastric Cancer collaborations, licensing, mergers and acquisition, funding, designations and other product related details. The assessment part of the report embraces, in depth Gastric Cancer commercial assessment and clinical assessment of the Gastric Cancer pipeline products under development.

 

Gastric Cancer Overview

Stomach cancer is cancer that starts anywhere inside the stomach or the stomach wall. It’s also called gastric cancer. Stomach cancer is more common in older people. Around 50 out of 100 cases (around 50%) occur in people aged 75 or over. It is more common in men than women. About 95% of the time, stomach cancer starts in the stomach lining and progresses slowly. Many stomach cancers are linked to lifestyle or environmental factors, including diet. Stomach cancer is linked with a bacteria that lives in the stomach called Helicobacter pylori. But not everyone with Helicobacter pylori will develop stomach cancer. Stomach cancer forms when there’s a genetic mutation (change) in the DNA of stomach cells. DNA is the code that tells cells when to grow and when to die. Because of the mutation, the cells grow rapidly and eventually form a tumor instead of dying. The cancer cells overtake healthy cells and may spread to other parts of the body (metastasize).

 

Find out more about Gastric Cancer Analysis @ Gastric Cancer Drugs

 

Gastric Cancer Emerging Drugs

  • Catumaxomab: Linton Pharm Co. Ltd.
  • HLX10: Shanghai Henlius Biotech
  • FLX475: RAPT Therapeutics
  • Savolitinib: AstraZeneca/HUTCHMED
  • ASP 2138: Astellas Pharma
  • Minnelide : Minneamrita Therapeutics LLC

 

Gastric Cancer Therapeutics Assessment

There are approx. 180+ Gastric Cancer companies which are developing the therapies for Gastric Cancer. The Gastric Cancer companies which have their Gastric Cancer drug candidates in the most advanced stage, i.e. phase III include, Linton Pharm Co. Ltd. The Gastric Cancer pipeline report proffers an integral view of the emerging Gastric Cancer segmented by stage, product type, molecule type, and route of administration.

 

Gastric Cancer pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as

  • Oral
  • Parenteral
  • Intravenous
  • Subcutaneous
  • Topical.

 

Dive deep into rich insights for new Gastric Cancer, visit @ Gastric Cancer Treatment Landscape 

 

Gastric Cancer Products have been categorized under various Molecule types such as

  • Monoclonal Antibody
  • Peptides
  • Polymer
  • Small molecule
  • Gene therapy

 

Scope of the Gastric Cancer Pipeline Report

  • Coverage- Global
  • Gastric Cancer Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
  • Gastric Cancer Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III
  • Gastric Cancer Companies- Linton Pharm Co.Ltd., Shanghai Henlius Biotech, RAPT Therapeutics, AstraZeneca, Astellas Pharma, Minneamrita Therapeutics, Aston Science, Servier Bio-Innovation LLC, Bukwang Pharmaceutical, TaihoOncology Inc., Novartis Pharmaceuticals, Base Therapeutics (Shanghai) Co. Ltd, Shanghai MiracogenInc., RemeGen Co Ltd., Idience Co. Ltd., BeiGene, Ono Pharmaceutical Co. Ltd, Elevar Therapeutics, R-Pharm, Innovent Biologics (Suzhou) Co.Ltd., Macro Genics, Sichuan Baili Pharmaceutical Co. Ltd., LianBio LLC, Janssen Pharmaceutical, and others.
  • Gastric Cancer Pipeline Therapies- S-1/Cisplatin, FLX475, Pembrolizumab, Tegafur-gimeracil-oteracil potassium, Oxaliplatin, Volitinib, Docetaxel, and others.

 

For further information on the Gastric Cancer Pipeline Therapeutics, reach out @ Gastric Cancer Therapeutics Segmentation

 

Table of Content

  1. Introduction
  2. Executive Summary
  3. Gastric Cancer: Overview
  4. Pipeline Therapeutics
  5. Therapeutic Assessment
  6. Late Stage Products (Phase III)
  7. Comparative Analysis
  8. Catumaxomab: Neovii Biotech
  9. Drug profiles in the detailed report…..
  10. Mid Stage Products (Phase II)
  11. FLX475: RAPT Therapeutics
  12. Early Stage Products (Phase I)
  13. Comparative Analysis
  14. ASP 2138: Astellas Pharma
  15. Inactive Products
  16. Gastric Cancer Key Companies
  17. Gastric Cancer Key Products
  18. Gastric Cancer – Unmet Needs
  19. Gastric Cancer – Market Drivers and Barriers
  20. Gastric Cancer – Future Perspectives and Conclusion
  21. Gastric Cancer Analyst Views
  22. Gastric Cancer Key Companies
  23. Appendix

 

Find out more about Gastric Cancer Therapeutics Assessment @ Gastric Cancer Preclinical and Discovery Stage Products

 

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Yash Bhardwaj
Email: Send Email
Phone: 9650213330
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: Nevada
Country: United States
Website: https://www.delveinsight.com/report-store/mouth-neoplasms-market

 

Press Release Distributed by ABNewswire.com

To view the original version on ABNewswire visit: Gastric Cancer Pipeline, Clinical Trials, FDA Approvals, Research and Developments, Future Perspectives, and Companies (Updated)

Colorectal Cancer Pipeline, Clinical Trials, FDA Approvals, Research and Developments, Future Perspectives, and Companies (Updated)

DelveInsight’s, “Colorectal Cancer Pipeline Insight 2023” report provides comprehensive insights about 195+ Colorectal Cancer companies and 200+ pipeline drugs in the Colorectal Cancer pipeline landscape. It covers the Colorectal Cancer pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Colorectal Cancer pipeline therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

 

Key Takeaways from the Colorectal Cancer Pipeline Report

  • DelveInsight’s Colorectal Cancer pipeline report depicts a robust space with 195+ companies working to develop 200+ pipeline Colorectal Cancer.
  • The leading Colorectal Cancer Companies working in the market include Exelixis, Mirati Therapeutics, Merck Sharp & Dohme LLC, Daiichi Sankyo Company, Inspirna, LyellI mmunopharma, Genentech, Cantargia AB, Arcus Biosciences Inc., Neogap Therapeutics AB, Criterium Inc., Daiichi Sankyo Inc., Bristol-Myers Squibb, Celyad Oncology SA, Pfizer, Akeso, Menarini Group, Elpiscience (Suzhou) Biopharma Ltd., Beyond Bio Inc., Shanghai Henlius Biotech, Rotta pharm Biotech, Innovative Cellular Therapeutics Inc., BioNTech SE, and others.
  • Promising Colorectal Cancer Pipeline Therapies in the various stages of development includes CPT-11 and TS-1, ZN-c3, Encorafenib, Cetuximab, Bevacizumab, Oxaliplatin, Capecitabine, Regorafenib (Stivarga, BAY73-4506), Leucovorin, and others.
  • January 2024: Daiichi Sankyo Inc. announced a study of Phase 2 clinical trials for DS-8201a 5.4 mg/kg Q3W. This study will evaluate the efficacy, safety, and pharmacokinetics of Trastuzumab deruxtecan (T-DXd) in participants with human epidermal growth factor 2 (HER2)-overexpressing locally advanced, unresectable, or metastatic colorectal cancer (mCRC).
  • December 2023: Bristol-Myers Squibb announced a study of Phase 3 clinical trials for Ipilimumab, Oxaliplatin, Leucovorin, Fluorouracil, and Irinotecan. The main purpose of this study is to compare the clinical benefit, as measured by Progression-Free Survival (PFS), Objective Response Rate (ORR), and Overall Survival (OS), achieved by nivolumab in combination with ipilimumab or by nivolumab monotherapy in participants with Microsatellite Instability High (MSI-H) or Mismatch Repair Deficient (dMMR) metastatic colorectal cancer (mCRC). This study will also compare nivolumab plus ipilimumab combination vs chemotherapy for treatment of MSI-H/dMMR mCRC participants.
  • December 2023: Genentech Inc. announced a study of Phase 1 clinical trials for BLYG8824A. This study will evaluate the safety, tolerability, and pharmacokinetics of BLYG8824A and will make a preliminary assessment of the anti-tumor activity of BLYG8824A in patients with locally advanced or metastatic colorectal cancer.
  • December 2023: Agenus Inc. announced a study of Phase 2 clinical trials for Botensilimab and Balstilimab. This is an open-label, Phase 2, multicenter study to evaluate the efficacy, safety, tolerability, and pharmacokinetic profiles of botensilimab as monotherapy and in combination with balstilimab or standard-of-care treatments in participants with refractory metastatic colorectal cancer.
  • December 2023: Novartis Pharmaceuticals announced a study of Phase 1 clinical trials for Dabrafenib, LTT462, Trametinib, LXH254, and TNO155. A phase Ib, open-label platform study of select drug combinations chosen in order to characterize safety and tolerability of each treatment arm tested and to identify recommended doses and regimens for future studies.

 

Request a sample and discover the recent advances in Colorectal Cancer Drugs @ Colorectal Cancer Pipeline Outlook Report

 

In the Colorectal Cancer Pipeline Report, detailed description of the drug is given which includes mechanism of action of the drug, Colorectal Cancer clinical trials studies, NDA approvals (if any), and product development activities comprising the technology, Colorectal Cancer collaborations, licensing, mergers and acquisition, funding, designations and other product related details. The assessment part of the report embraces, in depth Colorectal Cancer commercial assessment and clinical assessment of the Colorectal Cancer pipeline products under development.

 

Colorectal Cancer Overview

CRC is a multifactorial disease. The epithelial cells of colorectal mucosa can undergo hyperplasia, atypical hyperplasia (mild, moderate, or severe), and adenomas that can eventually develop into carcinoma. This process is usually initiated by carcinogenic factors, causing structural changes in DNA and leading to the malignant transformation of cells into cancer. Morphology includes epithelial hyperplasia, atypical hyperplasia, adenoma formation, carcinoma in situ, and invasive carcinoma.

 

Colorectal Cancer Emerging Drugs

  • XL092 : Exelixis
  • Adagrasb: Mirati Therapeutics
  • Olaparib : Merck Sharp & Dohme LLC/Astrazeneca
  • DS-8201: Daiichi Sankyo
  • Ompenaclid: Inspirna
  • LYL845: Lyell Immunopharma
  • RG6286: Genentech

 

Colorectal Cancer Therapeutics Assessment

There are approx. 195+ Colorectal Cancer companies which are developing the therapies for Colorectal Cancer. The Colorectal Cancer companies which have their Colorectal Cancer drug candidates in the most advanced stage, i.e. phase III include, Exelixis. The Colorectal Cancer pipeline report proffers an integral view of the emerging Colorectal Cancer segmented by stage, product type, molecule type, and route of administration.

 

Find out more about Colorectal Cancer Analysis @ Colorectal Cancer Drugs

  

DelveInsight’s Colorectal Cancer pipeline report covers around 200+ products under different phases of clinical development like

  • Late stage products (Phase III)
  • Mid-stage products (Phase II)
  • Early-stage product (Phase I) along with the details of
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates

 

Colorectal Cancer pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as

  • Oral
  • Intravenous
  • Subcutaneous
  • Parenteral
  • Topical

 

Colorectal Cancer Products have been categorized under various Molecule types such as

  • Recombinant fusion proteins
  • Small molecule
  • Monoclonal antibody
  • Peptide
  • Polymer
  • Gene therapy

 

Dive deep into rich insights for new Colorectal Cancer, visit @ Colorectal Cancer Treatment Landscape

 

Scope of the Colorectal Cancer Pipeline Report

  • Coverage- Global
  • Colorectal Cancer Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
  • Colorectal Cancer Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III
  • Colorectal Cancer Companies- Exelixis, Mirati Therapeutics, Merck Sharp & Dohme LLC, Daiichi Sankyo Company, Inspirna, LyellI mmunopharma, Genentech, Cantargia AB, Arcus Biosciences Inc., Neogap Therapeutics AB, Criterium Inc., Daiichi Sankyo Inc., Bristol-Myers Squibb, Celyad Oncology SA, Pfizer, Akeso, Menarini Group, Elpiscience (Suzhou) Biopharma Ltd., Beyond Bio Inc., Shanghai Henlius Biotech, Rotta pharm Biotech, Innovative Cellular Therapeutics Inc., BioNTech SE, and others.
  • Colorectal Cancer Pipeline Therapies- CPT-11 and TS-1, ZN-c3, Encorafenib, Cetuximab, Bevacizumab, Oxaliplatin, Capecitabine, Regorafenib (Stivarga, BAY73-4506), Leucovorin, and others.

 

For further information on the Colorectal Cancer Pipeline Therapeutics, reach out @ Colorectal Cancer Therapeutics Segmentation

 

Table of Content

  1. Introduction
  2. Colorectal Cancer Executive Summary
  3. Colorectal Cancer: Overview
  4. Colorectal Cancer Pipeline Therapeutics
  5. Colorectal Cancer Therapeutic Assessment
  6. Late Stage Products (Phase III)
  7. Comparative Analysis
  8. XL092: Exelixis
  9. Drug profiles in the detailed report…..
  10. Mid Stage Products (Phase II)
  11. Early Stage Products (Phase I)
  12. LYL845: Lyell Immunopharma
  13. Inactive Products
  14. Colorectal Cancer Key Companies
  15. Colorectal Cancer Products
  16. Colorectal Cancer Unmet Needs
  17. Colorectal Cancer Market Drivers and Barriers
  18. Colorectal Cancer Future Perspectives and Conclusion
  19. Colorectal Cancer Analyst Views
  20. Colorectal Cancer Key Companies
  21. Appendix

 

Find out more about Colorectal Cancer Therapeutics Assessment @ Colorectal Cancer Preclinical and Discovery Stage Products

 

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

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Yenny Zhang is Crafting a Distinct Narrative in Retail Design

Yenny Zhang is a dynamic retail designer who shapes immersive experiences with a unique blend of creativity and spatial expertise.

Yenny Zhang, a dynamic retail designer, is gaining recognition for her efforts in shaping immersive experiences that defy convention. Yenny Zhang brings a unique approach to her role. She not only designs seasonal retail spaces for Nike but also crafts compelling brand designs for clients and visually striking music videos for artists.

With an academic foundation in Environmental Design from the prestigious ArtCenter College of Design, Yenny’s distinctive skill set integrates creativity, spatial expertise, and a playful, experimental spirit. Her philosophy revolves around infusing playfulness into every audience, creating retail spaces that transcend mere transactions and evolve into captivating narratives.

Yenny’s noteworthy contributions to several Nike campaigns, including the Women’s World Cup 2023, Air Max Day 2023, Future Fitness, and World Cup 2022, showcase her ability to integrate creative branding into spatial experience design seamlessly. Her work is not just about showcasing products but crafting immersive stories that resonate profoundly with the audience.

Beyond her creative work for Nike, Yenny has collaborated with high-profile clients and artists, including Complex Media, 8UCK, Warner Music China, and Milly Rock Group. She has applied her creative touch to various projects, from internship to commercial design. Notably, her work on the Nike Capsule, a post-COVID reflection, and Genesis Oasis, a sponsored project focusing on the reconnecting of humans and nature, demonstrates her ability to address societal shifts through design.

Yenny’s projects extend beyond the traditional boundaries of retail, with highlights such as Upyard, her degree project, introducing a futuristic retail system that immerses consumers deeply in brand experiences. Her work showcases creativity, functionality, and a forward-thinking vision.

Yenny Zhang navigates the intersection of creative branding and spatial experience design, shaping immersive storytelling,” says one of Yenny’s coworkers. “Her approach has elevated the retail experience, turning the space into a unique and unforgettable journey.

In addition to her impactful projects, Yenny has received accolades and recognitions, including being the gold winner of the London Design Awards and being selected for the C-IDEA Design Award.

As a designer, Yenny Zhang’s impact goes beyond the physical spaces she creates. Her multidimensional approach to design extends into typography, motion graphics, sustainability, and hospitality. Notable projects like Dust, an exploration of Dyson’s products, and ReGene Resort, a sustainable spa resort, underscore her commitment to holistic and meaningful design.

Yenny Zhang’s work at the intersection of retail, branding, and immersive experiences is redefining the industry and setting a new standard for creative excellence. With a portfolio spanning from major global campaigns to innovative personal projects, Yenny continues to shape the future of retail design with a playful spirit and a commitment to transformative storytelling.

Users can visit the portfolio website of Yenny Zhang ydesignspaces.com, for any media or commercial inquiries.

For updates, follow Yenny Zhang on Instagram: https://www.instagram.com/ydesignspaces/

Media Contact
Company Name: ydesignspaces
Contact Person: Yenny Zhang
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City: Los Angeles
State: CA
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Website: ydesignspaces.com

 

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Latest Developments in Dry Eye Disease Pipeline – FDA Approvals, Clinical Trials, Therapies, MOA, ROA by DelveInsight | Leading Companies AbbVie, Allergan, AFT Pharma, Akorn, Alcon, Bausch Health, J&J

“Dry Eye Disease Pipeline”

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, Dry Eye Disease pipeline constitutes 45+ key companies continuously working towards developing 50+ Dry Eye Disease treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

The Dry Eye Disease Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers acquisition, funding, designations, and other product-related details.

 

Dry Eye Disease Pipeline Insight, 2023 report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Dry Eye Disease Market.

 

Some of the key takeaways from the Dry Eye Disease Pipeline Report:

  • Companies across the globe are diligently working toward developing novel Dry Eye Disease treatment therapies with a considerable amount of success over the years. 
  • Dry Eye Disease companies working in the treatment market are Quorum Innovations, Serentrix, IVIEW Therapeutics, Taejoon Pharmaceutical, Seinda Pharmaceutical, Invirsa, GL Pharm Tech Corporation, Dreamhawk Vision Biotech, Inc, Aramis Biosciences, Kowa Company, Alcon, HanAll Biopharma, Seikagaku Corporation, Novaliq GmbH, and others, are developing therapies for the Dry Eye Disease treatment 
  • Emerging Dry Eye Disease therapies in the different phases of clinical trials are- Qi 401, SER-114, iVIEW 1001, TJO-083, SY-201, INV-102, GLH8NDE, SHJ 002, A197, K-161, AR-15512, HL036, SI-614, NOV03, CyclASol, and others are expected to have a significant impact on the Dry Eye Disease market in the coming years.   
  • In February 2023, “Novaliq revealed intentions to submit a Marketing Authorization Application (MAA) for CyclASol (ciclosporin ophthalmic solution), an innovative anti-inflammatory remedy aimed at addressing dry eye disease (DED) within the European Union.”
  • In November 2022, “Alcon declared the successful finalization of its acquisition of Aerie Pharmaceuticals. This acquisition has broadened Alcon’s portfolio with commercial products including netarsudil and latanoprost ophthalmic solution (Rocklatan) 0.02%/0.005% and netarsudil ophthalmic solution (Rhopressa) 0.02%, alongside AR-15512, a Phase 3 product in development for treating dry eye disease.”
  • In October 2022, “Aldeyra Therapeutics, Inc. concluded the phase 3 clinical study involving 0.25% reproxalap ophthalmic solution, an experimental medication under investigation for allergic conjunctivitis treatment. The company showcased the trial’s clinical findings at the American Academy of Optometry’s 2022 Annual Meeting.”
  • In October 2022, “Novaliq revealed that the U.S. Food and Drug Administration (FDA) had approved the New Drug Application (NDA) for CyclASol® (cyclosporine ophthalmic solution), an innovative anti-inflammatory remedy specifically designed to address the signs and symptoms of dry eye disease (DED). In the United States, the FDA has established a Prescription Drug User Fee Act (PDUFA) target action date for the CyclASol® New Drug Application (NDA).”
  • In November 2022, “Aerie Pharmaceuticals commenced a year-long, multicenter, double-masked, randomized Phase 3 trial, conducted at around 10 locations across the United States. All participants included in the study will be diagnosed with dry eye disease (DED). The trial will involve visits at Baseline (Day 1) as well as on Day 14, Day 90, Day 180, Day 270, and Day 365 (Study Exit).”
  • In January 2022, “NovaBay Pharmaceuticals introduced Avenova lubricating eye drops designed to address symptoms associated with dry eyes.”

 

Dry Eye Disease Overview

A lack of tear film homeostasis is the cause of dry eye disease (DED), also referred to as dry eye syndrome (DES), keratoconjunctivitis sicca (KCS), and keratitis sicca. DED is a multifactorial illness of the ocular surface.

 

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Emerging Dry Eye Disease Drugs Under Different Phases of Clinical Development Include:

  • Qi 401: Quorum Innovations
  • SER-114: Serentrix
  • iVIEW 1001: IVIEW Therapeutics
  • TJO-083: Taejoon Pharmaceutical
  • SY-201: Seinda Pharmaceutical
  • INV-102: Invirsa
  • GLH8NDE: GL Pharm Tech Corporation
  • SHJ 002: Dreamhawk Vision Biotech, Inc
  • A197: Aramis Biosciences
  • K-161: Kowa Company
  • AR-15512: Alcon
  • HL036: HanAll Biopharma
  • SI-614: Seikagaku Corporation
  • NOV03: Novaliq GmbH
  • CyclASol: Novaliq GmbH

 

Dry Eye Disease Route of Administration

Dry Eye Disease pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs, such as 

  • Oral
  • Intravenous
  • Subcutaneous
  • Parenteral
  • Topical

 

Dry Eye Disease Molecule Type

Dry Eye Disease Products have been categorized under various Molecule types, such as

  • Recombinant fusion proteins
  • Small molecule
  • Monoclonal antibody
  • Peptide
  • Polymer
  • Gene therapy

 

Dry Eye Disease Pipeline Therapeutics Assessment

  • Dry Eye Disease Assessment by Product Type
  • Dry Eye Disease By Stage and Product Type
  • Dry Eye Disease Assessment by Route of Administration
  • Dry Eye Disease By Stage and Route of Administration
  • Dry Eye Disease Assessment by Molecule Type
  • Dry Eye Disease by Stage and Molecule Type

 

DelveInsight’s Dry Eye Disease Report covers around 50+ products under different phases of clinical development like

  • Late-stage products (Phase III)
  • Mid-stage products (Phase II)
  • Early-stage product (Phase I)
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates
  • Route of Administration

 

Further Dry Eye Disease product details are provided in the report. Download the Dry Eye Disease pipeline report to learn more about the emerging Dry Eye Disease therapies

 

Some of the key companies in the Dry Eye Disease Therapeutics Market include:

Key companies developing therapies for Dry Eye Disease are – AbbVie Inc. (Allergan PLC), AFT Pharmaceuticals, Akorn, Alcon Inc., Bausch Health Companies Inc., Horus Pharma, Johnson & Johnson, Mitotech, Novaliq GmbH, OASIS Medical, Otsuka Pharmaceutical Co. Ltd, Prestige Consumer Healthcare, Santen Pharmaceutical Co. Ltd, Sentiss Pharma Pvt. Ltd, Sun Pharmaceutical Industries Ltd, VISUfarma, and others.

 

Dry Eye Disease Pipeline Analysis:

The Dry Eye Disease pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Dry Eye Disease with aggregate therapies developed by each company for the same.
  • It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Dry Eye Disease Treatment.
  • Dry Eye Disease key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Dry Eye Disease Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type. 
  • Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Dry Eye Disease market.

The report is built using data and information traced from the researcher’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university websites and industry-specific third-party sources, etc.

 

Download Sample PDF Report to know more about Dry Eye Disease drugs and therapies

 

Dry Eye Disease Pipeline Market Drivers

  • Rise in geriatric population, increasing Exposure to computer screens, increased R&D Activities, adoption of new Technologies are some of the important factors that are fueling the Dry Eye Disease Market.

 

Dry Eye Disease Pipeline Market Barriers

  • However, lack of awareness about dry eye disease in low income countries, complexity of the disease, challenges associated with the Ocular drug delivery and other factors are creating obstacles in the Dry Eye Disease Market growth.

 

Scope of Dry Eye Disease Pipeline Drug Insight    

  • Coverage: Global
  • Key Dry Eye Disease Companies: Quorum Innovations, Serentrix, IVIEW Therapeutics, Taejoon Pharmaceutical, Seinda Pharmaceutical, Invirsa, GL Pharm Tech Corporation, Dreamhawk Vision Biotech, Inc, Aramis Biosciences, Kowa Company, Alcon, HanAll Biopharma, Seikagaku Corporation, Novaliq GmbH, and others
  • Key Dry Eye Disease Therapies: Qi 401, SER-114, iVIEW 1001, TJO-083, SY-201, INV-102, GLH8NDE, SHJ 002, A197, K-161, AR-15512, HL036, SI-614, NOV03, CyclASol, and others
  • Dry Eye Disease Therapeutic Assessment: Dry Eye Disease current marketed and Dry Eye Disease emerging therapies
  • Dry Eye Disease Market Dynamics: Dry Eye Disease market drivers and Dry Eye Disease market barriers 

 

Request for Sample PDF Report for Dry Eye Disease Pipeline Assessment and clinical trials

 

Table of Contents

1. Dry Eye Disease Report Introduction

2. Dry Eye Disease Executive Summary

3. Dry Eye Disease Overview

4. Dry Eye Disease- Analytical Perspective In-depth Commercial Assessment

5. Dry Eye Disease Pipeline Therapeutics

6. Dry Eye Disease Late Stage Products (Phase II/III)

7. Dry Eye Disease Mid Stage Products (Phase II)

8. Dry Eye Disease Early Stage Products (Phase I)

9. Dry Eye Disease Preclinical Stage Products

10. Dry Eye Disease Therapeutics Assessment

11. Dry Eye Disease Inactive Products

12. Company-University Collaborations (Licensing/Partnering) Analysis

13. Dry Eye Disease Key Companies

14. Dry Eye Disease Key Products

15. Dry Eye Disease Unmet Needs

16 . Dry Eye Disease Market Drivers and Barriers

17. Dry Eye Disease Future Perspectives and Conclusion

18. Dry Eye Disease Analyst Views

19. Appendix

20. About DelveInsight

 

About DelveInsight

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

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Influenza Pipeline Report: Recent Approvals by FDA, EMA, and PMDA, Emerging Therapies, Clinical Trials, and Growth Outlook | AlloVir, Osivax, CureVac AG, GlaxoSmithKline, Cocrystal Pharma Inc.

“Influenza Pipeline”

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, Influenza pipeline constitutes 120+ key companies continuously working towards developing 120+ Influenza treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

The Influenza Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers acquisition, funding, designations, and other product-related details.

 

Influenza Pipeline Insight, 2023 report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Influenza Market.

 

Some of the key takeaways from the Influenza Pipeline Report: 

  • Companies across the globe are diligently working toward developing novel Influenza treatment therapies with a considerable amount of success over the years. 
  • Influenza companies working in the treatment market are Arcturus Therapeutics, Emergex Vaccines, Emergent Biosolutions, Cocrystal Pharma Inc, GlaxoSmithKline, CureVac AG, AlloVir, Moderna, OSIVAX, Ena Respiratory, Valenta Pharmaceuticals, Raynovent Co., Ltd, and others, are developing therapies for the Influenza treatment 
  • Emerging Influenza therapies in the different phases of clinical trials are- LUNAR-FLU, naNO-Flu, UniFlu, CC-42344,GSK4382276A, CVSQIV, ALVR 106, mRNA-1073, OVX836, Neumifil, INNA-051, mRNA-1010, XC-221, ZSP1273, and others are expected to have a significant impact on the Influenza market in the coming years.   
  • In July 2022, Emergex Vaccines Holding Limited has achieved the production of its universal/pandemic influenza vaccine designed for Phase I clinical trials, utilizing fully synthetic CD8+ T cell Adaptive Vaccines.
  • CureVac has initiated the dosing of the initial participant in a Phase I trial for the modified influenza vaccine FLU SV mRNA, developed in partnership with GSK. This trial comes subsequent to the commencement of another Phase I study in February 2022, assessing an unmodified, multivalent influenza vaccine candidate, CVSQIV, across clinical sites in Panama. Both studies aim to present combined data upon completion.
  • In June 2022, Moderna, Inc. revealed the initiation of dosing in a Phase III trial for its seasonal influenza vaccine candidate, mRNA-1010, with the initial participants receiving doses. Anticipated to enroll about 6,000 adults in Southern Hemisphere nations, this Phase III randomized, observer-blind study aims to assess the safety and immune response of mRNA-1010 compared to a licensed seasonal influenza vaccine in adults aged 18 years and above.
  • In April 2022, Novavax, Inc. released preliminary findings from the Phase I/II clinical trial of its COVID-Influenza Combination Vaccine (CIC). The CIC merges Novavax’s COVID-19 vaccine, NVX-CoV2373, with its quadrivalent influenza vaccine candidate. The trial confirmed the viability of formulating this combined vaccine, showing good tolerance and immune response.
  • In April 2022, Osivax has announced the publication of Phase IIa results for its universal influenza vaccine candidate, OVX836, titled “Randomized, Double-Blind, Reference-Controlled, Phase IIa Study Evaluating the Immunogenicity and Safety of OVX836, A Nucleoprotein-Based Influenza Vaccine” in the journal Frontiers in Immunology. Utilizing Osivax’s self-assembling nanoparticle technology, OVX836 focuses on an internal nucleoprotein (NP), an antigen less prone to frequent mutations compared to surface antigens of the influenza virus.
  • BioNTech and Pfizer have joined forces to develop an influenza vaccine utilizing BioNTech’s mRNA platforms. In July 2022, data from the Phase II expansion study of BNT161 in participants aged 65 and older revealed initial evidence of significantly enhanced induction of strain-specific CD4+ and CD8+ responses. The geometric mean fold rise (GMFR) was notably higher compared to the control quadrivalent influenza vaccine for both CD4+ and CD8+ strain-specific T cell responses. Encouraged by these promising T cell responses and observed seroconversion, plans are underway to commence a Phase III study for the quadrivalent modified mRNA influenza vaccine in the latter half of 2022.
  • In May 2022, Blue Water Vaccines revealed a partnership with the Center for R&D in Immunobiologics, part of the Instituto Butantan, to advance BWV’s universal influenza candidate, BWV-101, in Brazil. Butantan stands as the primary flu vaccine producer in the Southern Hemisphere, responsible for manufacturing all influenza vaccine doses employed by the Brazilian Ministry of Health.

 

Influenza Overview

A contagious virus that affects the upper respiratory system, including the upper and lower respiratory passages, called influenza.It is caused by a broad range of influenza viruses. While some of these viruses are unique to particular species, others can infect humans.

 

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Emerging Influenza Drugs Under Different Phases of Clinical Development Include:

  • LUNAR-FLU: Arcturus Therapeutics
  • naNO-Flu: Emergex Vaccines
  • UniFlu: Emergent Biosolutions
  • CC-42344: Cocrystal Pharma Inc
  • GSK4382276A: GlaxoSmithKline
  • CVSQIV: CureVac AG
  • ALVR 106: AlloVir
  • mRNA-1073: Moderna
  • OVX836: OSIVAX
  • Neumifil: Pneumagen Ltd.
  • INNA-051: Ena Respiratory
  • mRNA-1010: Moderna, Inc.
  • XC-221: Valenta Pharmaceuticals
  • ZSP1273: Raynovent Co., Ltd

 

Influenza Route of Administration

Influenza pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs, such as 

  • Inhalation
  • Inhalation/Intravenous/Oral
  • Intranasal
  • Intravenous
  • Intravenous/ Subcutaneous
  • NA
  • Oral
  • Oral/intranasal/subcutaneous
  • Parenteral
  • Subcutaneous

 

Influenza Molecule Type

Influenza Products have been categorized under various Molecule types, such as

  • Antibody
  • Antisense oligonucleotides
  • Immunotherapy
  • Monoclonal antibody
  • Peptides
  • Protein
  • Recombinant protein
  • Small molecule
  • Stem Cell
  • Vaccine

 

Influenza Pipeline Therapeutics Assessment

  • Influenza Assessment by Product Type
  • Influenza By Stage and Product Type
  • Influenza Assessment by Route of Administration
  • Influenza By Stage and Route of Administration
  • Influenza Assessment by Molecule Type
  • Influenza by Stage and Molecule Type

 

DelveInsight’s Influenza Report covers around 120+ products under different phases of clinical development like

  • Late-stage products (Phase III)
  • Mid-stage products (Phase II)
  • Early-stage product (Phase I)
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates
  • Route of Administration

 

Further Influenza product details are provided in the report. Download the Influenza pipeline report to learn more about the emerging Influenza therapies

 

Some of the key companies in the Influenza Therapeutics Market include:

Key companies developing therapies for Influenza are – AlloVir, Osivax, CureVac AG, GlaxoSmithKline, Cocrystal Pharma Inc, Viriom, Emergent BioSolutions, Pfizer, Moderna, SAB Biotherapeutics, ENA Respiratory Pty Ltd, Codagenix, Jiangxi Qingfeng Pharmaceutical Co. Ltd., Guangdong Raynovent Biotech Co., Ltd, FluGen Inc, BlueWillow Biologics, AVM Biotechnology LLC, Ansun Biopharma, Inc., Guangzhou Henovcom Bioscience, Sunshine Lake Pharma Co., Ltd., Emergex Vaccines, Vir Biotechnology, CSL Limited, Novavax, Mitsubishi Chemical Group Corporation, Poolbeg Pharma, MYMETICS, CELLTRION INC, and others.

 

Influenza Pipeline Analysis:

The Influenza pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Influenza with aggregate therapies developed by each company for the same.
  • It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Influenza Treatment.
  • Influenza key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Influenza Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type. 
  • Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Influenza market.

The report is built using data and information traced from the researcher’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university websites and industry-specific third-party sources, etc.

 

Download Sample PDF Report to know more about Influenza drugs and therapies

 

Influenza Pipeline Market Drivers

  • Increasing awareness by government authorities, increasing clinical trials for new product development, increase in investment by leading market players are some of the important factors that are fueling the Influenza Market.

 

Influenza Pipeline Market Barriers

  • However, longer process for novel vaccine development, high cost of vaccine development other factors are creating obstacles in the Influenza Market growth.

 

Scope of Influenza Pipeline Drug Insight    

  • Coverage: Global
  • Key Influenza Companies: Arcturus Therapeutics, Emergex Vaccines, Emergent Biosolutions, Cocrystal Pharma Inc, GlaxoSmithKline, CureVac AG, AlloVir, Moderna, OSIVAX, Ena Respiratory, Valenta Pharmaceuticals, Raynovent Co., Ltd, and others
  • Key Influenza Therapies: LUNAR-FLU, naNO-Flu, UniFlu, CC-42344,GSK4382276A, CVSQIV, ALVR 106, mRNA-1073, OVX836, Neumifil, INNA-051, mRNA-1010, XC-221, ZSP1273, and others
  • Influenza Therapeutic Assessment: Influenza current marketed and Influenza emerging therapies
  • Influenza Market Dynamics: Influenza market drivers and Influenza market barriers 

 

Request for Sample PDF Report for Influenza Pipeline Assessment and clinical trials

 

Table of Contents

1. Influenza Report Introduction

2. Influenza Executive Summary

3. Influenza Overview

4. Influenza- Analytical Perspective In-depth Commercial Assessment

5. Influenza Pipeline Therapeutics

6. Influenza Late Stage Products (Phase II/III)

7. Influenza Mid Stage Products (Phase II)

8. Influenza Early Stage Products (Phase I)

9. Influenza Preclinical Stage Products

10. Influenza Therapeutics Assessment

11. Influenza Inactive Products

12. Company-University Collaborations (Licensing/Partnering) Analysis

13. Influenza Key Companies

14. Influenza Key Products

15. Influenza Unmet Needs

16 . Influenza Market Drivers and Barriers

17. Influenza Future Perspectives and Conclusion

18. Influenza Analyst Views

19. Appendix

20. About DelveInsight

 

About DelveInsight

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Ankit Nigam
Email: Send Email
Phone: +91-9650213330
Address:304 S. Jones Blvd #2432
City: Albany
State: New York
Country: United States
Website: https://www.delveinsight.com/consulting/conference-coverage-services

 

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To view the original version on ABNewswire visit: Influenza Pipeline Report: Recent Approvals by FDA, EMA, and PMDA, Emerging Therapies, Clinical Trials, and Growth Outlook | AlloVir, Osivax, CureVac AG, GlaxoSmithKline, Cocrystal Pharma Inc.

Assessment of Non-Hodgkin Lymphoma Pipeline and Clinical Trials in 2023: FDA Approvals, Therapeutics, and Key Companies by DelveInsight | AstraZeneca, Baxter, Bayer, Bristol Myers Squibb, Teva Pharma

“Non-Hodgkin Lymphoma Pipeline”

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, Non-Hodgkin Lymphoma pipeline constitutes key companies continuously working towards developing Non-Hodgkin Lymphoma treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

The Non-Hodgkin Lymphoma Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers acquisition, funding, designations, and other product-related details.

 

Non-Hodgkin Lymphoma Pipeline Insight, 2023 report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Non-Hodgkin Lymphoma Market.

 

Some of the key takeaways from the Non-Hodgkin Lymphoma Pipeline Report:

  • Companies across the globe are diligently working toward developing novel Non-Hodgkin Lymphoma treatment therapies with a considerable amount of success over the years. 
  • Non-Hodgkin Lymphoma companies working in the treatment market are Autolus, Genor Biopharma, AbbVie/ Genmab, AstraZeneca, Jiangsu Hengrui Medicine, Pacylex Pharmaceuticals, Zentera Therapeutics, TCR2 Therapeutics, Artiva Biotherapeutics, Loxo Oncology, Angiocrine Bioscience, AbbVie, Novartis, and others, are developing therapies for the Non-Hodgkin Lymphoma treatment 
  • Emerging Non-Hodgkin Lymphoma therapies in the different phases of clinical trials are- AUTO4, GB226, Epcoritamab, Capivasertib, HRS-3738, PCLX-001, ZN-d5, TC-110, AB-101, LOXO-305, AB-205, Venetoclax, Tisagenlecleucel, and others are expected to have a significant impact on the Non-Hodgkin Lymphoma market in the coming years.   
  • In May 2023, The US FDA has granted approval for the investigational new drug (IND) application submitted by SIRPant Immuno therapeutics. This approval allows the commencement of a phase I clinical trial, marking the first time the treatment will be tested in humans, aimed at addressing relapsed refractory non-Hodgkin lymphoma.
  • In May 2023, The US FDA has granted approval to AbbVie for EPKINLY (epcoritamab-bysp), a T-cell engaging bispecific antibody designed for treating adult patients experiencing relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL).

 

Non-Hodgkin Lymphoma Overview

A malignancy of the lymphatic system is called non-Hodgkin’s lymphoma (NHL). It happens when lymphocytes give rise to tumors. One variety of white blood cell is the lymphocyte. NHL is more prevalent than lymphoma Hodgkin’s. The presence of a particular kind of aberrant cell known as the Reed-Sternberg cell is the primary distinction between NHL and Hodgkin’s lymphoma.

 

Get a Free Sample PDF Report to know more about Non-Hodgkin Lymphoma Pipeline Therapeutic Assessment-

https://www.delveinsight.com/report-store/non-hodgkins-lymphoma-nhl-pipeline-insight 

 

Emerging Non-Hodgkin Lymphoma Drugs Under Different Phases of Clinical Development Include:

  • AUTO4: Autolus
  • GB226: Genor Biopharma
  • Epcoritamab: AbbVie/ Genmab
  • Capivasertib: AstraZeneca
  • HRS-3738: Jiangsu Hengrui Medicine
  • PCLX-001: Pacylex Pharmaceuticals
  • ZN-d5: Zentera Therapeutics
  • TC-110: TCR2 Therapeutics
  • AB-101: Artiva Biotherapeutics
  • LOXO-305: Loxo Oncology
  • AB-205: Angiocrine Bioscience
  • Venetoclax: AbbVie
  • Tisagenlecleucel: Novartis 

 

Non-Hodgkin Lymphoma Pipeline Therapeutics Assessment

  • Non-Hodgkin Lymphoma Assessment by Product Type
  • Non-Hodgkin Lymphoma By Stage and Product Type
  • Non-Hodgkin Lymphoma Assessment by Route of Administration
  • Non-Hodgkin Lymphoma By Stage and Route of Administration
  • Non-Hodgkin Lymphoma Assessment by Molecule Type
  • Non-Hodgkin Lymphoma by Stage and Molecule Type

 

DelveInsight’s Non-Hodgkin Lymphoma Report covers around products under different phases of clinical development like

  • Late-stage products (Phase III)
  • Mid-stage products (Phase II)
  • Early-stage product (Phase I)
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates
  • Route of Administration

 

Further Non-Hodgkin Lymphoma product details are provided in the report. Download the Non-Hodgkin Lymphoma pipeline report to learn more about the emerging Non-Hodgkin Lymphoma therapies

 

Some of the key companies in the Non-Hodgkin Lymphoma Therapeutics Market include:

Key Non-Hodgkin Lymphoma companies developing therapies for Non-Hodgkin Lymphoma are – AstraZeneca, Baxter International Inc., Bayer AG, Bristol Myers Squibb Company, Teva Pharmaceutical Industries Ltd, Eli Lilly and Co., F. Hoffmann La-Roche Ltd, GlaxoSmithKline PLC, and others.

 

Non-Hodgkin Lymphoma Pipeline Analysis:

The Non-Hodgkin Lymphoma pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Non-Hodgkin Lymphoma with aggregate therapies developed by each company for the same.
  • It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Non-Hodgkin Lymphoma Treatment.
  • Non-Hodgkin Lymphoma key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Non-Hodgkin Lymphoma Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type. 
  • Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Non-Hodgkin Lymphoma market.

The report is built using data and information traced from the researcher’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university websites and industry-specific third-party sources, etc.

 

Download Sample PDF Report to know more about Non-Hodgkin Lymphoma drugs and therapies

 

Non-Hodgkin Lymphoma Pipeline Market Drivers

  • Increasing prevalence, ongoing and increased R&D activity, demand for innovative drugs and novel therapies are some of the important factors that are fueling the Non-Hodgkin Lymphoma Market.

 

Non-Hodgkin Lymphoma Pipeline Market Barriers

  • However, high cost of treatment, complications related to the drugs and other factors are creating obstacles in the Non-Hodgkin Lymphoma Market growth.

 

Scope of Non-Hodgkin Lymphoma Pipeline Drug Insight    

  • Coverage: Global
  • Key Non-Hodgkin Lymphoma Companies: Autolus, Genor Biopharma, AbbVie/ Genmab, AstraZeneca, Jiangsu Hengrui Medicine, Pacylex Pharmaceuticals, Zentera Therapeutics, TCR2 Therapeutics, Artiva Biotherapeutics, Loxo Oncology, Angiocrine Bioscience, AbbVie, Novartis, and others
  • Key Non-Hodgkin Lymphoma Therapies: AUTO4, GB226, Epcoritamab, Capivasertib, HRS-3738, PCLX-001, ZN-d5, TC-110, AB-101, LOXO-305, AB-205, Venetoclax, Tisagenlecleucel, and others
  • Non-Hodgkin Lymphoma Therapeutic Assessment: Non-Hodgkin Lymphoma current marketed and Non-Hodgkin Lymphoma emerging therapies
  • Non-Hodgkin Lymphoma Market Dynamics: Non-Hodgkin Lymphoma market drivers and Non-Hodgkin Lymphoma market barriers 

 

Request for Sample PDF Report for Non-Hodgkin Lymphoma Pipeline Assessment and clinical trials

 

Table of Contents

1. Non-Hodgkin Lymphoma Report Introduction

2. Non-Hodgkin Lymphoma Executive Summary

3. Non-Hodgkin Lymphoma Overview

4. Non-Hodgkin Lymphoma- Analytical Perspective In-depth Commercial Assessment

5. Non-Hodgkin Lymphoma Pipeline Therapeutics

6. Non-Hodgkin Lymphoma Late Stage Products (Phase II/III)

7. Non-Hodgkin Lymphoma Mid Stage Products (Phase II)

8. Non-Hodgkin Lymphoma Early Stage Products (Phase I)

9. Non-Hodgkin Lymphoma Preclinical Stage Products

10. Non-Hodgkin Lymphoma Therapeutics Assessment

11. Non-Hodgkin Lymphoma Inactive Products

12. Company-University Collaborations (Licensing/Partnering) Analysis

13. Non-Hodgkin Lymphoma Key Companies

14. Non-Hodgkin Lymphoma Key Products

15. Non-Hodgkin Lymphoma Unmet Needs

16 . Non-Hodgkin Lymphoma Market Drivers and Barriers

17. Non-Hodgkin Lymphoma Future Perspectives and Conclusion

18. Non-Hodgkin Lymphoma Analyst Views

19. Appendix

20. About DelveInsight

 

About DelveInsight

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Ankit Nigam
Email: Send Email
Phone: +91-9650213330
Address:304 S. Jones Blvd #2432
City: Albany
State: New York
Country: United States
Website: https://www.delveinsight.com/consulting

 

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To view the original version on ABNewswire visit: Assessment of Non-Hodgkin Lymphoma Pipeline and Clinical Trials in 2023: FDA Approvals, Therapeutics, and Key Companies by DelveInsight | AstraZeneca, Baxter, Bayer, Bristol Myers Squibb, Teva Pharma

Projected Surge in Psychosis in Parkinson’s and Alzheimer’s Disease Market from 2023 to 2032: Analysis by DelveInsight on Sunovion Pharmaceuticals and Vanda Pharma

“Psychosis in Parkinson’s and Alzheimer’s Disease Market”

DelveInsight’s “Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Psychosis in Parkinson’s Disease and Alzheimer’s Disease, historical and forecasted epidemiology as well as the Psychosis in Parkinson’s Disease and Alzheimer’s Disease market trends in the United States, EU4 (Germany, Spain, Italy, France) the United Kingdom and Japan.

 

To Know in detail about the Psychosis in Parkinson’s Disease and Alzheimer’s Disease market outlook, drug uptake, treatment scenario and epidemiology trends, Click here; Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Forecast

 

Some of the key facts of the Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Report: 

  • The Psychosis in Parkinson’s Disease and Alzheimer’s Disease market size was valued approximately USD 1,229 million in 2022 and is anticipated to grow with a significant CAGR during the study period (2019-2032)
  • Acadia’s NUPLAZID (pimavanserin) stands as the sole approved product for PDP (Parkinson’s Disease Psychosis) in the US. While it is still under investigation for ADP (Alzheimer’s Disease Psychosis), it carries a boxed warning concerning heightened mortality risks observed in elderly patients with psychosis related to dementia.
  • Several medications are in various stages of development to address psychosis in Parkinson’s Disease and Alzheimer’s Disease, yet only a limited number are in advanced stages. Examples include Karuna Therapeutics’ KarXT (xanomeline-trospium), Sunovion Pharmaceuticals’ Ulotaront (SEP-363856), and Vanda Pharmaceuticals’ FANAPT (iloperidone). These are expected to be introduced to the market within the forecast period spanning from 2023 to 2032.
  • In 2022, the combined diagnosed prevalent cases of Psychosis in PD (Parkinson’s Disease) and AD (Alzheimer’s Disease) across the 7MM reached around 6,737,337 cases. Projections indicate an anticipated increase by 2032 at a Compound Annual Growth Rate (CAGR) of 2.4% throughout the study period from 2019 to 2032.
  • In 2022, the United States represented approximately 34% of the diagnosed prevalent cases of Psychosis in PD (Parkinson’s Disease) and AD (Alzheimer’s Disease) within the 7MM. This proportion is anticipated to rise further by the year 2032.
  • In the United States, there were an estimated 675,948 cases in males and 503,305 cases in females affected by PD (Parkinson’s Disease) in 2022. These figures are projected to rise by the year 2032
  • In the year 2022, the number of AD (Alzheimer’s Disease) cases among males in EU4 and the UK was approximately 1,454,541, while among females, it reached nearly 3,487,835 cases. These figures are anticipated to increase by the year 2032.
  • In 2022, Germany contributed to roughly 18% of the total diagnosed prevalent cases of PD (Parkinson’s Disease) within the 7MM. These cases are projected to rise at a Compound Annual Growth Rate (CAGR) of 1.7% during the study period from 2019 to 2032.
  • Key Psychosis in Parkinson’s Disease and Alzheimer’s Disease Companies: Karuna Therapeutics, Sunovion Pharmaceuticals, Vanda Pharmaceuticals, Intra-Cellular Therapeutics, Merck Sharp & Dohme, and others
  • Key Psychosis in Parkinson’s Disease and Alzheimer’s Disease Therapies: KarXT, Ulotaront, FANAPT, ITI-1284, MK-8189, and others
  • The Parkinson’s Disease epidemiology based on gender analyzed that in the US, males diagnosed with PD are higher in number than females
  • The Psychosis in Parkinson’s Disease and Alzheimer’s Disease market is expected to surge due to the disease’s increasing prevalence and awareness during the forecast period. Furthermore, launching various multiple-stage Psychosis in Parkinson’s Disease and Alzheimer’s Disease pipeline products will significantly revolutionize the Psychosis in Parkinson’s Disease and Alzheimer’s Disease market dynamics.

 

Psychosis in Parkinson’s Disease and Alzheimer’s Disease Overview

The National Institute of Mental Health (NIMH) defines psychosis as a group of symptoms affecting the mind in which there has been a partial loss of reality awareness. People have disruptions in their thoughts and perceptions during a psychotic episode, making it difficult for them to distinguish between reality and illusion.

In Parkinson’s disease (PD) and Alzheimer’s disease (AD), psychosis develops as a result of both endogenous (associated with the disease process) and exogenous (drugs, for example).

 

Get a Free sample for the Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Forecast, Size & Share Analysis Report: 

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Psychosis in Parkinson’s Disease and Alzheimer’s Disease Epidemiology

The epidemiology section provides insights into the historical, current, and forecasted epidemiology trends in the seven major countries (7MM) from 2019 to 2032. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. The epidemiology section also provides a detailed analysis of the diagnosed patient pool and future trends.

 

Psychosis in Parkinson’s Disease and Alzheimer’s Disease Epidemiology Segmentation:

The Psychosis in Parkinson’s Disease and Alzheimer’s Disease market report proffers epidemiological analysis for the study period 2019–2032 in the 7MM segmented into:

  • Total Prevalence of Psychosis in Parkinson’s Disease and Alzheimer’s Disease
  • Prevalent Cases of Psychosis in Parkinson’s Disease and Alzheimer’s Disease by severity
  • Gender-specific Prevalence of Psychosis in Parkinson’s Disease and Alzheimer’s Disease
  • Diagnosed Cases of Episodic and Chronic Psychosis in Parkinson’s Disease and Alzheimer’s Disease

 

Download the report to understand which factors are driving Psychosis in Parkinson’s Disease and Alzheimer’s Disease epidemiology trends @ Psychosis in Parkinson’s Disease and Alzheimer’s Disease Epidemiology Forecast

 

Psychosis in Parkinson’s Disease and Alzheimer’s Disease Drugs Uptake and Pipeline Development Activities

The drugs uptake section focuses on the rate of uptake of the potential drugs recently launched in the Psychosis in Parkinson’s Disease and Alzheimer’s Disease market or expected to get launched during the study period. The analysis covers Psychosis in Parkinson’s Disease and Alzheimer’s Disease market uptake by drugs, patient uptake by therapies, and sales of each drug. 

Moreover, the therapeutics assessment section helps understand the drugs with the most rapid uptake and the reasons behind the maximal use of the drugs. Additionally, it compares the drugs based on market share.

The report also covers the Psychosis in Parkinson’s Disease and Alzheimer’s Disease Pipeline Development Activities. It provides valuable insights about different therapeutic candidates in various stages and the key companies involved in developing targeted therapeutics. It also analyzes recent developments such as collaborations, acquisitions, mergers, licensing patent details, and other information for emerging therapies.

 

Psychosis in Parkinson’s Disease and Alzheimer’s Disease Therapies and Key Companies

  • KarXT: Karuna Therapeutics
  • Ulotaront: Sunovion Pharmaceuticals
  • FANAPT: Vanda PharmaceuticalsF
  • ITI-1284: Intra-Cellular Therapeutics
  • MK-8189: Merck Sharp & Dohme

 

Discover more about therapies set to grab major Psychosis in Parkinson’s Disease and Alzheimer’s Disease market share @ Psychosis in Parkinson’s Disease and Alzheimer’s Disease Treatment Landscape

 

Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Strengths

  • Increased awareness and a more in-depth understanding of the disease pathophysiology has improved diagnosis and treatment.
  • The recent US FDA approval of NUPLAZID, the first approved therapy for treating hallucinations and delusions associated with PD Psychosis, indicates a positive change in treatment paradigm.

 

Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Opportunities

  • There are opportunities for pharma players to develop therapies with improved safety and tolerability profiles, effectively reducing symptoms and preventing the recurrence of Psychosis in PD and AD.
  • Advancement in biomarkers for cognitive decline allows precise diagnosis and individualized treatments

 

Scope of the Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Report

  • Study Period: 2019–2032
  • Coverage: 7MM [The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan]
  • Key Psychosis in Parkinson’s Disease and Alzheimer’s Disease Companies: Karuna Therapeutics, Sunovion Pharmaceuticals, Vanda Pharmaceuticals, Intra-Cellular Therapeutics, Merck Sharp & Dohme, and others
  • Key Psychosis in Parkinson’s Disease and Alzheimer’s Disease Therapies: KarXT, Ulotaront, FANAPT, ITI-1284, MK-8189, and others
  • Psychosis in Parkinson’s Disease and Alzheimer’s Disease Therapeutic Assessment: Psychosis in Parkinson’s Disease and Alzheimer’s Disease current marketed and Psychosis in Parkinson’s Disease and Alzheimer’s Disease emerging therapies
  • Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Dynamics: Psychosis in Parkinson’s Disease and Alzheimer’s Disease market drivers and Psychosis in Parkinson’s Disease and Alzheimer’s Disease market barriers 
  • Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter’s five forces, BCG Matrix, Market entry strategies
  • Psychosis in Parkinson’s Disease and Alzheimer’s Disease Unmet Needs, KOL’s views, Analyst’s views, Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Access and Reimbursement 

 

To know more about Psychosis in Parkinson’s Disease and Alzheimer’s Disease companies working in the treatment market, visit @ Psychosis in Parkinson’s Disease and Alzheimer’s Disease Clinical Trials and Therapeutic Assessment

 

Table of Contents 

1. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Report Introduction

2. Executive Summary for Psychosis in Parkinson’s Disease and Alzheimer’s Disease

3. SWOT analysis of Psychosis in Parkinson’s Disease and Alzheimer’s Disease

4. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Patient Share (%) Overview at a Glance

5. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Overview at a Glance

6. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Disease Background and Overview

7. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Epidemiology and Patient Population

8. Country-Specific Patient Population of Psychosis in Parkinson’s Disease and Alzheimer’s Disease 

9. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Current Treatment and Medical Practices

10. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Unmet Needs

11. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Emerging Therapies

12. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Outlook

13. Country-Wise Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Analysis (2019–2032)

14. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Access and Reimbursement of Therapies

15. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Drivers

16. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Market Barriers

17.  Psychosis in Parkinson’s Disease and Alzheimer’s Disease Appendix

18. Psychosis in Parkinson’s Disease and Alzheimer’s Disease Report Methodology

19. DelveInsight Capabilities

20. Disclaimer

21. About DelveInsight

 

About DelveInsight 

DelveInsight is a leading Healthcare Business Consultant, and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance.

It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate the business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Ankit Nigam
Email: Send Email
Phone: +91-9650213330
Address:304 S. Jones Blvd #2432
City: Albany
State: New York
Country: United States
Website: https://www.delveinsight.com/consulting

 

Press Release Distributed by ABNewswire.com

To view the original version on ABNewswire visit: Projected Surge in Psychosis in Parkinson’s and Alzheimer’s Disease Market from 2023 to 2032: Analysis by DelveInsight on Sunovion Pharmaceuticals and Vanda Pharma

Assessment of RNA Interference Pipeline and Clinical Trials in 2023: FDA Approvals, Therapeutics, and Companies by DelveInsight | Moderna Therapeutics, GenSight Biologics, Pfizer, bluebird bio

“RNA Interference Pipeline”

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, RNA interference pipeline constitutes 20+ key companies continuously working towards developing 90+ RNA interference treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

The RNA interference Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers acquisition, funding, designations, and other product-related details.

 

RNA interference Pipeline Insight, 2023 report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the RNA interference Market.

 

Some of the key takeaways from the RNA interference Pipeline Report:

  • Companies across the globe are diligently working toward developing novel RNA interference treatment therapies with a considerable amount of success over the years. 
  • RNA interference companies working in the treatment market are Olix Pharmaceuticals, Phio Pharmaceutic als, Siranomics, Arbutus Biopharma, Bio-Path Holdings, Vir Biotechnology, Alnylam Pharmaceuticals, Sylentis, and others, are developing therapies for the RNA interference treatment 
  • Emerging RNA interference therapies in the different phases of clinical trials are- OLX 703A, PH 894, STP707, AB-729, BP1001, VIR-2218, Cemdisiran, SYL1001, Lumasiran, and others are expected to have a significant impact on the RNA interference market in the coming years.   
  • In October 2022, Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), a leading RNAi therapeutics company, has announced that the U.S. Food and Drug Administration (FDA) has approved an expansion to the label for OXLUMO® (lumasiran), an RNAi therapeutic administered via subcutaneous injection. This expansion now includes an indication for treating primary hyperoxaluria type 1 (PH1) to reduce urinary oxalate (UOx) and plasma oxalate (POx) levels in both pediatric and adult patients. The FDA’s decision is supported by positive efficacy and safety findings from the ILLUMINATE-C Phase 3 study, which involved patients with severe renal impairment, including those receiving hemodialysis.
  • In October 2022, Regeneron Pharmaceuticals has commenced a Phase III clinical trial that is randomized and open-label, comparing pozelimab and cemdisiran in combination. This study aims to evaluate the safety and effectiveness of this therapy combination in patients diagnosed with paroxysmal nocturnal hemoglobinuria. These patients are currently undergoing treatment with eculizumab or ravulizumab. The trial is currently in an active phase and is not recruiting new participants. It is anticipated to conclude by June 2025.

 

RNA interference Overview

One of the mechanisms known as RNA silencing pathways, which use short RNAs as guides for sequence-specific silencing, is RNA interference (RNAi). Long double-stranded RNA (dsRNA)-induced sequence-specific mRNA degradation is known as RNAi, and it was first identified in C. elegans. In almost all human cells, the RNA interference (RNAi) pathway controls mRNA stability and translation.

 

Get a Free Sample PDF Report to know more about RNA interference Pipeline Therapeutic Assessment-

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Emerging RNA interference Drugs Under Different Phases of Clinical Development Include:

  • OLX 703A: Olix Pharmaceuticals
  • PH 894: Phio Pharmaceutic als
  • STP707: Siranomics
  • AB-729: Arbutus Biopharma
  • BP1001: Bio-Path Holdings
  • VIR-2218: Vir Biotechnology
  • Cemdisiran: Alnylam Pharmaceuticals
  • SYL1001: Sylentis
  • Lumasiran: Alnylam Pharmaceuticals

 

RNA interference Route of Administration

RNA interference pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs, such as 

  • Intra-articular
  • Intraocular
  • Intrathecal
  • Intravenous
  • Ophthalmic
  • Oral
  • Parenteral
  • Subcutaneous
  • Topical
  • Transdermal

 

RNA interference Molecule Type

RNA interference Products have been categorized under various Molecule types, such as

  • Oligonucleotide
  • Peptide
  • Small molecule

 

RNA interference Pipeline Therapeutics Assessment

  • RNA interference Assessment by Product Type
  • RNA interference By Stage and Product Type
  • RNA interference Assessment by Route of Administration
  • RNA interference By Stage and Route of Administration
  • RNA interference Assessment by Molecule Type
  • RNA interference by Stage and Molecule Type

 

DelveInsight’s RNA interference Report covers around 90+ products under different phases of clinical development like

  • Late-stage products (Phase III)
  • Mid-stage products (Phase II)
  • Early-stage product (Phase I)
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates
  • Route of Administration

 

Further RNA interference product details are provided in the report. Download the RNA interference pipeline report to learn more about the emerging RNA interference therapies

 

Some of the key companies in the RNA interference Therapeutics Market include:

Key companies developing therapies for RNA interference are – Moderna Therapeutics, GenSight Biologics, Pfizer, bluebird bio, CureVac, ReGenX Biosciences, TransCode Therapeutics, Bicycle Therapeutics, and others.

 

RNA interference Pipeline Analysis:

The RNA interference pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of RNA interference with aggregate therapies developed by each company for the same.
  • It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for RNA interference Treatment.
  • RNA interference key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • RNA interference Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type. 
  • Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the RNA interference market.

The report is built using data and information traced from the researcher’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university websites and industry-specific third-party sources, etc.

 

Download Sample PDF Report to know more about RNA interference drugs and therapies

 

RNA interference Pipeline Market Drivers

Increasing prevalence of genetic disorders and other chronic medical conditions, diverse and extensive pipeline therapies, rise in the number of geriatric population are some of the important factors that are fueling the RNA interference Market.

 

RNA interference Pipeline Market Barriers

However, RNAi silencing method suffers from high off-target effects, high cost of research and development and other factors are creating obstacles in the RNA interference Market growth.

 

Scope of RNA interference Pipeline Drug Insight    

  • Coverage: Global
  • Key RNA interference Companies: Olix Pharmaceuticals, Phio Pharmaceutic als, Siranomics, Arbutus Biopharma, Bio-Path Holdings, Vir Biotechnology, Alnylam Pharmaceuticals, Sylentis, and others
  • Key RNA interference Therapies: OLX 703A, PH 894, STP707, AB-729, BP1001, VIR-2218, Cemdisiran, SYL1001, Lumasiran, and others
  • RNA interference Therapeutic Assessment: RNA interference current marketed and RNA interference emerging therapies
  • RNA interference Market Dynamics: RNA interference market drivers and RNA interference market barriers 

 

Request for Sample PDF Report for RNA interference Pipeline Assessment and clinical trials

 

Table of Contents

1. RNA interference Report Introduction

2. RNA interference Executive Summary

3. RNA interference Overview

4. RNA interference- Analytical Perspective In-depth Commercial Assessment

5. RNA interference Pipeline Therapeutics

6. RNA interference Late Stage Products (Phase II/III)

7. RNA interference Mid Stage Products (Phase II)

8. RNA interference Early Stage Products (Phase I)

9. RNA interference Preclinical Stage Products

10. RNA interference Therapeutics Assessment

11. RNA interference Inactive Products

12. Company-University Collaborations (Licensing/Partnering) Analysis

13. RNA interference Key Companies

14. RNA interference Key Products

15. RNA interference Unmet Needs

16 . RNA interference Market Drivers and Barriers

17. RNA interference Future Perspectives and Conclusion

18. RNA interference Analyst Views

19. Appendix

20. About DelveInsight

 

About DelveInsight 

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Ankit Nigam
Email: Send Email
Phone: +91-9650213330
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City: Albany
State: New York
Country: United States
Website: https://www.delveinsight.com/consulting

 

Press Release Distributed by ABNewswire.com

To view the original version on ABNewswire visit: Assessment of RNA Interference Pipeline and Clinical Trials in 2023: FDA Approvals, Therapeutics, and Companies by DelveInsight | Moderna Therapeutics, GenSight Biologics, Pfizer, bluebird bio