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“Ulcerative Colitis Treatment Market”

(Albany, USA) DelveInsight’s Ulcerative Colitis Market report offers a detailed comprehension of the Ulcerative Colitis market size by treatment, epidemiology, and emerging therapies. The report also provides an understanding of Ulcerative Colitis market share of the individual therapies, current and forecasted Ulcerative Colitis market size from 2020 to 2034 segmented into 7MM (the USA, EU5 (the UK, Italy, Spain, France, and Germany), and Japan).

The Ulcerative Colitis market report provides current treatment practices, emerging drugs, the market share of the individual therapies, and the current and forecasted Ulcerative Colitis market size from 2020 to 2034, segmented by seven major markets. The Report also covers current Ulcerative Colitis treatment practice/algorithm, market drivers, market barriers, and unmet medical needs to curate the best opportunities and assesses the underlying potential of the Ulcerative Colitis market.

To know more in detail about Ulcerative Colitis Market report offerings, click here @ Ulcerative Colitis Market Forecast

Key highlights from the Ulcerative Colitis Market Insight report

• According to DelveInsight, the Ulcerative Colitis market size is expected to grow at a decent CAGR by 2034.
• The total Ulcerative Colitis Market Size in the 7MM was approximately USD 8090 million in 2022 and is projected to increase during the forecast period (2023–2034).
• In the United States, the total number of diagnosed prevalent cases of ulcerative colitis was 1,437,600 in 2022.
• Leading Ulcerative Colitis companies working proactively in the therapeutic market are Janssen Pharmaceuticals, Takeda Pharmaceuticals, Pfizer, EA Pharma, Kissei Pharma, Gilead Sciences, Galapagos NV, Celgene (Bristol-Myers Squibb), AbbVie, Arena Pharmaceuticals, Reistone Biopharma, Landos Biopharma, Bridge Biotherapeutics, Applied Molecular Transport, AbGenomics (AltruBio), Abivax, Connect Biopharma, Boehringer Ingelheim, Eli Lilly and Company, InDex Pharmaceuticals, Bristol-Myers Squibb, Protagonist Therapeutics, Mesoblast Ltd, and several others in the clinical development stage for Ulcerative Colitis will lead to a significant increase in the market size during the forecast period.
• The key Ulcerative Colitis therapies expected to launch in the market include Jyseleca (filgotinib), Rinvoq (Upadacitinib), Skyrizi (Risankizumab), Mirikizumab (LY-3074828), Etrasimod, Tremfya (Guselkumab), Izencitinib (TD-1473/ JNJ 8398), BT-11, and others.
• According to DelveInsight analysis, the Ulcerative Colitis market is expected to rise in the coming years due to the entry of novel therapies with better clinical profile and patient convenient RoA, increase in market penetration of targeted/ advanced therapies, increasing prevalence of Ulcerative Colitis, and new biomarkers for diagnosis of Ulcerative Colitis.
• In March 2025, Palisade Bio, Inc. (Nasdaq: PALI) (“Palisade”, “Palisade Bio”, or the “Company”), a clinical-stage biopharmaceutical company focused on developing and advancing novel therapeutics for patients living with autoimmune, inflammatory, and fibrotic diseases, today provided an update on its ongoing Phase 1a/b study of PALI-2108 for the treatment of Ulcerative Colitis (UC).
• In February 2025, Equillium, Inc. (Nasdaq: EQ), a clinical-stage biotechnology company leveraging a deep understanding of immunobiology to develop novel therapeutics to treat severe autoimmune and inflammatory disorders, and Biocon Limited (BSE code: 532523, NSE: BIOCON), an innovation-led global biopharmaceutical company, today announced positive topline results from the Phase 2 study evaluating itolizumab in the treatment of moderate to severe ulcerative colitis (UC).
• In January 2025, Abivax SA (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company developing innovative therapies to address chronic inflammatory diseases, today announced a significant milestone in the Phase 3 ABTECT clinical trial evaluating obefazimod for the treatment of moderately to severely active UC.
• In September 2024, Johnson & Johnson (NYSE: JNJ) today announced that the U.S. Food and Drug Administration (FDA) has approved TREMFYA® (guselkumab) for the treatment of adults with moderately to severely active ulcerative colitis (UC), a chronic disease of the large intestine in which the lining of the colon becomes inflamed. TREMFYA® is the first and only approved fully-human, dual-acting monoclonal antibody that blocks IL-23 while also binding to CD64, a receptor on cells that produce IL-23. IL-23 is a cytokine secreted by activated monocyte/macrophages and dendritic cells that is known to be a driver of immune-mediated diseases including UC.
• In August 2024, Abivax SA (Euronext Paris & Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, announced today that in July 2024, the 600th participant was enrolled in the Phase 3 ABTECT Trial. Based on this milestone and current enrollment pace, the Company reaffirms expectations to reach full enrollment in early Q1 2025.
• On April 2024, Vedanta Biosciences announced results of A Phase 2 double-blind, placebo-controlled, randomized study to evaluate the safety, efficacy, and microbiota changes of VE202 in biologic-naïve patients with mild to moderate Ulcerative Colitis. In Parts 1 and 2 of the study, patients will receive VE202 or placebo for 8 weeks or 2 weeks. In Part 3, patients will be followed for safety for 1 year from the start of treatment.
• On March 2024, Eli Lilly announced results of a Multicenter, Phase 3b, Open-Label, Single-Arm Study to Investigate Bowel Urgency and Its Relationship with Other Outcome Measures in Adults With Moderately to Severely Active Ulcerative Colitis Treated With Mirikizumab.

For further information on Market Impact by Therapies, Download Ulcerative Colitis Market sample @ https://www.delveinsight.com/sample-request/ulcerative-colitis-uc-market

Ulcerative Colitis Overview

Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD) that causes inflammation and ulcers in the lining of the colon and rectum. It is an autoimmune condition in which the immune system mistakenly attacks the intestinal lining, leading to symptoms such as abdominal pain, persistent diarrhea, rectal bleeding, weight loss, and fatigue. The severity of symptoms varies, with periods of flare-ups and remission.

The exact cause of ulcerative colitis is unknown, but genetic factors, immune system dysfunction, and environmental triggers are believed to play a role. It is commonly diagnosed in young adults between 15 and 30 years old. Diagnosis involves clinical evaluation, blood tests, stool tests, colonoscopy, and imaging studies.

Treatment focuses on reducing inflammation and managing symptoms. Mild to moderate cases are treated with aminosalicylates (5-ASA drugs) like mesalamine, while corticosteroids, immunosuppressants, and biologic therapies (such as TNF inhibitors and JAK inhibitors) are used for more severe cases. In refractory cases or complications like toxic megacolon, surgery (colectomy) may be required.

While ulcerative colitis has no cure, early diagnosis and proper treatment can improve quality of life. Ongoing research into new biologics and microbiome-based therapies offers hope for better disease management.

Ulcerative Colitis Epidemiology Segmentation

DelveInsight’s analysts indicate that the total diagnosed cases of Ulcerative Colitis in the 7MM were 1,577,979 in 2020. These cases are expected to rise by 2034, during the forecast period.

The Ulcerative Colitis market report proffers epidemiological analysis for the study period 2020-32 in the 7MM segmented into:

• Total Prevalent Ulcerative Colitis Cases
• Total Diagnosed Prevalent Ulcerative Colitis Cases
• Age-Specific Diagnosed Prevalent Cases of Ulcerative Colitis
• Severity-Specific Diagnosed Prevalent Cases of Ulcerative Colitis
• Total Treated Ulcerative Colitis Cases

Download Ulcerative Colitis Market sample to know more about the epidemiology and market trends @ Ulcerative colitis Prevalence

Ulcerative Colitis Pipeline Therapies and Key Companies

• Jyseleca (filgotinib): Gilead Sciences/Galapagos NV
• Rinvoq (Upadacitinib) & Skyrizi(Risankizumab): AbbVie
• Risankizumab (ABBV-066): AbbVie and Boehringer Ingelheim
• Mirikizumab (LY-3074828): Eli Lilly and Company
• Etrasimod: Arena Pharmaceuticals
• Tremfya (Guselkumab): Janssen (Johnson & Johnson)
• Izencitinib (TD-1473/ JNJ 8398): Theravance Biopharma/Johnson & Johnson
• BT-11: Landos Biopharma

Ulcerative Colitis Market Dynamics

The current therapeutic landscape of Ulcerative Colitis in the 7MM is driven by several approved therapies. Also, the Ulcerative Colitis market is expected to surge due to factors such as the increasing prevalence of Ulcerative Colitis, entry of novel therapies with better clinical profile and patient convenient RoA, increase in market penetration of targeted/ advanced therapies, new biomarkers for diagnosis of Ulcerative Colitis and also the involvement of digital technology for diagnosis and treatment.

A high number of undiagnosed and unreported cases contribute to the lack of awareness of Ulcerative Colitis. The entry of biosimilars in the Ulcerative Colitis Market, insufficient knowledge of the disease, and significant drawbacks of existing therapeutic options may act as certain obstructions in the Ulcerative Colitis market.

For further information on Market Impact by Therapies, Download Ulcerative Colitis Market sample @ Ulcerative colitis Medication and Companies

Scope of the Ulcerative Colitis Market Report

• Study Period: 2020-34
• Coverage: 7MM [The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan]
• Key Ulcerative Colitis Companies: Takeda Pharmaceutical, Pfizer, Celgene (Bristol-Myers Squibb), Gilead Sciences, Galapagos NV, AbbVie, Eli Lilly and Company, Arena Pharmaceuticals, Janssen (Johnson & Johnson), Theravance Biopharma, Landos Biopharma
• Key Ulcerative Colitis Drugs: Jyseleca (filgotinib), Rinvoq (Upadacitinib), Skyrizi(Risankizumab), Mirikizumab (LY-3074828), Etrasimod, Tremfya (Guselkumab), Izencitinib (TD-1473/ JNJ 8398), BT-11
• Ulcerative Colitis Therapeutic Assessment: Ulcerative Colitis current marketed and emerging therapies
• Ulcerative Colitis Market Dynamics: Ulcerative Colitis market drivers and barriers
• Competitive Intelligence Analysis: Porter’s five forces, SWOT analysis, PESTLE analysis, Market entry strategies, BCG Matrix, Unmet Needs
• KOL views
• Reimbursement Scenario

Download Market sample to know more about the recent happenings in the Ulcerative colitis therapeutic landscape @ Ulcerative colitis Clinical Trials and Advancements

Table of Contents

1. Key Insights

2. Report Introduction of Ulcerative Colitis

3. Ulcerative Colitis Market Overview at a Glance

4. Executive Summary of Ulcerative Colitis

5. Ulcerative Colitis Epidemiology and Market Forecast Flow

6. Ulcerative Colitis: Disease Background and Overview

7. Ulcerative Colitis Diagnosis

8. Ulcerative Colitis Current Treatment

9. Ulcerative Colitis Epidemiology and Patient Population

10. Ulcerative Colitis Patient Journey

11. Key Endpoints in Ulcerative Colitis Clinical Trials

12. Ulcerative Colitis Marketed Therapies of Ulcerative Colitis

13. Ulcerative Colitis Emerging Therapies

14. Conjoint Analysis of Ulcerative Colitis

15. Ulcerative Colitis: Seven Major Market Analysis

16. The United States Market Size

17. Ulcerative Colitis Market Access and Reimbursement

18. Ulcerative Colitis Market Drivers

19. Ulcerative Colitis Market Barriers

20. Ulcerative Colitis SWOT Analysis

21. Ulcerative Colitis Unmet Needs

22. Appendix

23. DelveInsight Capabilities

24. Disclaimer

25. About DelveInsight

About DelveInsight

DelveInsight is a pioneer in stipulating state-of-the-art services to the clients, also serving as 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. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve.

Media Contact
Company Name: DelveInsight Business Research LLP
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“Obesity Treatment Market”

(Albany, USA) DelveInsight’s “Obesity Market Insights, Epidemiology, and Market Forecast-2034” report delivers an in-depth understanding of Obesity, historical and forecasted epidemiology as well as the Obesity market trends in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom), and Japan.

The Obesity market report provides current treatment practices, emerging drugs, the market share of the individual therapies, and the current and forecasted Obesity market size from 2020 to 2034, segmented by seven major markets. The Report also covers current Obesity treatment practice/algorithm, market drivers, market barriers, and unmet medical needs to curate the best opportunities and assesses the underlying potential of the Obesity market.

Request for a Free Sample Report @ Obesity Market Forecast

Some facts of the Obesity Market Report are:

• In March 2025, Novo Nordisk launched NovoCare® Pharmacy, a direct-to-patient delivery service, to ensure access to Wegovy® (semaglutide) injection in all dose strengths (0.25 mg, 0.5 mg, 1 mg, 1.7 mg, and 2.4 mg). This service offers uninsured patients or those with commercial insurance lacking obesity medicine coverage the option to purchase Wegovy® at a reduced cost of $499 per month. This initiative expands Novo Nordisk’s efforts to meet the needs of individuals living with obesity, following the FDA’s confirmation that the shortage of the medication has been resolved and that all doses now meet or exceed U.S. demand.
• In February 2025, Eli Lilly launched 7.5 mg and 10 mg Zepbound (tirzepatide) vials for $499 through the Zepbound Self Pay Journey Program, alongside price reductions for 2.5 mg and 5 mg vials. These are available exclusively via LillyDirect Self Pay Pharmacy Solutions, offering direct savings outside of insurance.
• In February 2025, Amgen announced that the U.S. FDA has placed a hold on a study of the company’s early-stage obesity candidate, AMG 513, marking another potential setback in its efforts to enter the growing weight loss drug market. Amgen has provided limited information about the drug, including its mechanism of action.
• In January 2025, Novo Nordisk reported that a high dose of its obesity drug Wegovy led to greater weight loss than the approved regimen in a Phase III trial. However, the data also suggest that Eli Lilly’s rival GLP-1 drug Zepbound may still have an advantage over Wegovy.
• In January 2025, Verdiva Bio Limited launched as a clinical-stage biopharmaceutical company focused on innovative therapies for obesity and cardiometabolic disorders. The company is advancing next-generation oral and injectable treatments and raised $411M in an oversubscribed Series A round, co-led by Forbion and General Atlantic, with participation from RA Capital Management, OrbiMed, Logos Capital, Lilly Asia Ventures, and LYFE Capital.
• In January 2025, Eli Lilly filed a motion to intervene as a defendant in a case between the Outsourcing Facilities Association and FarmaKeio Custom Compounding against the FDA. The court has ordered the Outsourcing Facilities Association to respond by January 15, with Eli Lilly’s reply due by January 21.
• As per DelveInsight’s estimates, the United States accounted for the highest number of total prevalent cases of Obesity among the 7MM in 2023.
• DelveInsight’s consultant estimates that adult patients constituted the maximum number of cases of obesity patients seeking help in 2023.
• According to the findings, treatment rate for children was found to be less than that of adults across countries.
• Among EU4 and the UK, the highest number of treated cases of obesity in adults was observed in the United Kingdom in 2023, which is followed by Germany.
• The leading Obesity Companies such as Rhythm Pharmaceuticals, Boehringer Ingelhium, D&D Pharmatech, ProQR Therapeutics, Nano Precision Medical, Bukwang Pharmaceutical, Caliway Biopharmaceutics, Yuhan, Terns Pharmaceuticals, BioRestorative Therapies, SCOHIA PHARMA, Click Therapeutics, Hanmi Pharmaceuticals, Novo Nordisk, Empros Pharma, Carmot Therapeutics, Eli Lilly and Company, and others
• Promising Obesity Therapies such as IMCIVREE (setmelanotide), ZEPBOUND (tirzepatide), Semaglutide oral, Survodutide (BI 456906), DD03, AX-0601, NPM 139, BK-1701, CBW-520, YH34160, TERN-601, Thermostem, SCO-267, CT-181, HM15136, NNC0480-0389, EMP-16, CT-868, Semaglutide, and others.
• On June 2023, Eli Lilly and Company (NYSE: LLY) announced the new phase 2 data from retatrutide, Lilly’s investigational molecule being studied for the treatment of obesity. At 24 weeks, retatrutide (1 mg, 4 mg, 8 mg or 12 mg) met the primary endpoint for the efficacy estimand in participants living with obesity or overweight without diabetes, demonstrating a mean weight reduction up to 17.5% (41.2 lb. or 18.7 kg). In a secondary endpoint, retatrutide demonstrated a mean weight reduction up to 24.2% (57.8 lb. or 26.2 kg)ii at the end of the 48-week treatment duration.
• On June 2023, Pfizer (NYSE: PFE) updated that it is scrapping its once-a-day experimental obesity pill because of concerns about liver safety, but will continue developing its other obesity pill, the twice-daily treatment danuglipron, as it races to rival the success of other weight loss treatments.
• On May 2023, Novo Nordisk (NYSE: NVO) announced positive results from a phase IIIa study, OASIS 1, in the global OASIS program for a once-daily oral formulation of semaglutide in obesity.

Obesity Overview

Obesity is a chronic condition characterized by an excessive accumulation of body fat, leading to adverse health effects and increased risk of various diseases. It is typically defined by a body mass index (BMI) of 30 or higher. Obesity results from complex interactions between genetic, environmental, socioeconomic, and behavioral factors. Sedentary lifestyles, high-calorie diets, and genetic predispositions contribute to its development. Obesity is associated with numerous health complications, including type 2 diabetes, cardiovascular disease, hypertension, certain cancers, and musculoskeletal disorders. Additionally, it can impair quality of life and increase mortality rates. Prevention and management strategies for obesity include dietary modifications, regular physical activity, behavioral therapy, medications, and in severe cases, bariatric surgery. Public health initiatives and policies aimed at promoting healthy lifestyles and reducing obesity prevalence are essential to address this global epidemic and its associated health burdens.

Learn more about Obesity treatment algorithms in different geographies, and patient journeys. Contact to receive a sample @ https://www.delveinsight.com/sample-request/weight-loss-weight-management-obesity-market

Obesity Market

The Obesity market outlook of the report helps to build a detailed comprehension of the historical, current, and forecasted Obesity market trends by analyzing the impact of current Obesity therapies on the market and unmet needs, and drivers, barriers, and demand for better technology.

This segment gives a thorough detail of the Obesity market trend of each marketed drug and late-stage pipeline therapy by evaluating their impact based on the annual cost of therapy, inclusion and exclusion criteria, mechanism of action, compliance rate, growing need of the market, increasing patient pool, covered patient segment, expected launch year, competition with other therapies, brand value, their impact on the market and view of the key opinion leaders. The calculated Obesity market data are presented with relevant tables and graphs to give a clear view of the market at first sight.

According to DelveInsight, the Obesity market in 7MM is expected to witness a major change in the study period 2020-2034.

Obesity Epidemiology

The Obesity epidemiology section provides insights into the historical and current Obesity patient pool and forecasted trends for seven individual major countries. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. This part of the Obesity market report also provides the diagnosed patient pool, trends, and assumptions.

Explore more about Obesity Epidemiology @ Obesity Market Dynamics

Obesity Drugs Uptake

This section focuses on the uptake rate of the potential Obesity drugs recently launched in the Obesity market or expected to be launched in 2020-2034. The analysis covers the Obesity market uptake by drugs, patient uptake by therapies, and sales of each drug.

Obesity Drugs Uptake helps in understanding the drugs with the most rapid uptake and the reasons behind the maximal use of new drugs and allows the comparison of the drugs based on Obesity market share and size, which again will be useful in investigating factors important in market uptake and in making financial and regulatory decisions.

Obesity Pipeline Development Activities

The Obesity report provides insights into different therapeutic candidates in Phase II, and Phase III stages. It also analyses Obesity key players involved in developing targeted therapeutics.

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Obesity Therapeutics Assessment

Major key companies are working proactively in the Obesity Therapeutics market to develop novel therapies which will drive the Obesity treatment markets in the upcoming years are Novo Nordisk, Eli Lilly and Company, MedImmune, Boehringer Ingelheim, Raziel Therapeutics, Altimmune, Saniona, YSOPIA Bioscience, Innovent Biologics, Glaceum, Shionogi, Aardvark Therapeutics, NuSirt Biopharma, Novartis, CSPC Baike (Shandong) Biopharmaceutical, Jiangsu HengRui Medicine, Carmot Therapeutics, Pfizer, Sciwind Biosciences, Empros Pharma and others.

Learn more about the emerging Obesity therapies & key companies @ Obesity Clinical Trials and Advancements

Obesity Report Key Insights

1. Obesity Patient Population

2. Obesity Market Size and Trends

3. Key Cross Competition in the Obesity Market

4. Obesity Market Dynamics (Key Drivers and Barriers)

5. Obesity Market Opportunities

6. Obesity Therapeutic Approaches

7. Obesity Pipeline Analysis

8. Obesity Current Treatment Practices/Algorithm

9. Impact of Emerging Therapies on the Obesity Market

Table of Contents

1. Key Insights

2. Executive Summary

3. Obesity Competitive Intelligence Analysis

4. Obesity Market Overview at a Glance

5. Obesity Disease Background and Overview

6. Obesity Patient Journey

7. Obesity Epidemiology and Patient Population

8. Obesity Treatment Algorithm, Current Treatment, and Medical Practices

9. Obesity Unmet Needs

10. Key Endpoints of Obesity Treatment

11. Obesity Marketed Products

12. Obesity Emerging Therapies

13. Obesity Seven Major Market Analysis

14. Attribute Analysis

15. Obesity Market Outlook (7 major markets)

16. Obesity Access and Reimbursement Overview

17. KOL Views on the Obesity Market

18. Obesity Market Drivers

19. Obesity Market Barriers

20. Appendix

21. DelveInsight Capabilities

22. Disclaimer

About DelveInsight

DelveInsight is a leading Life Science market research and business consulting company recognized for its off-the-shelf syndicated market research reports and customized solutions to firms in the healthcare sector.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Ankit Nigam
Email: Send Email
Phone: +14699457679
Address:304 S. Jones Blvd #2432
City: Albany
State: New York
Country: United States
Website: https://www.delveinsight.com/aacr-annual-meeting

Press Release Distributed by ABNewswire.com

To view the original version on ABNewswire visit: Obesity Treatment Market 2034: EMA, PDMA, FDA Approvals, Clinical trials, Medication, Statistics, Revenue, Therapies, Prevalence and Companies by DelveInsight

“Spinal Muscular Atrophy Clinical Trials”

(Albany, USA) “Spinal Muscular Atrophy Pipeline Insight, 2025″ report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Spinal Muscular Atrophy Market.

Spinal Muscular Atrophy pipeline constitutes 18+ key companies continuously working towards developing 20+ Spinal Muscular Atrophy treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

The Spinal Muscular Atrophy clinical trials 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.

To know more in detail about Spinal Muscular Atrophy pipeline report offerings, click here: Spinal Muscular Atrophy Clinical Trials and Pipeline

Some of the key takeaways from the Spinal Muscular Atrophy Pipeline Report:

• In March 2025, Scholar Rock (NASDAQ: SRRK), a late-stage biopharmaceutical company focused on advancing innovative treatments for neuromuscular diseases, cardiometabolic disorders, and other serious diseases, today announced that the U.S. Food and Drug Administration (FDA) has accepted its Biologics License Application (BLA) for apitegromab, an investigational muscle-targeted treatment that is being developed to provide clinically meaningful improvement in motor function for people living with spinal muscular atrophy (SMA) who are receiving an SMN-targeted treatment. The FDA will review the application under priority review and has assigned a Prescription Drug User Fee Act (PDUFA) target action date of September 22, 2025. The FDA priority review designation conveys that the FDA has determined that if apitegromab is approved, it could offer significant improvement in the safety or effectiveness of treatment of the serious condition of SMA
• Spinal Muscular Atrophy Companies across the globe are diligently working toward developing novel Spinal Muscular Atrophy treatment therapies with a considerable amount of success over the years.
• Leading Spinal Muscular Atrophy companies working in the market are Scholar Rock, Biogen, Astellas Pharma, Alcyone Therapeutics, AndroScience Corporation, Hanugen Theraputics, Voyager Therapeutics, Hoffmann-La Roche, Catalyst Pharmaceuticals, NMD Pharma, Biohaven Pharmaceuticals, CANbridge Pharmaceuticals Inc., Aurimed Pharma, Exicure, Amylon Therapeutics, Amniotics, and others, are developing therapies for the Spinal Muscular Atrophy treatment
• Spinal Muscular Atrophy emerging therapies such as – ACTX-401, Apitegromab, GYM329, and others are expected to have a significant impact on the Spinal Muscular Atrophy market in the coming years.
• In February 2025, Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), announced today that the U.S. Food and Drug Administration (FDA) has approved a New Drug Application (NDA) for an Evrysdi® (risdiplam) tablet for people living with spinal muscular atrophy (SMA). Evrysdi is the only non-invasive disease-modifying treatment for SMA. The 5 mg Evrysdi tablet can either be swallowed whole or dispersed in water.
• In January 2025, Biogen Inc. (Nasdaq: BIIB) announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s supplemental New Drug Application (sNDA) and the European Medicines Agency (EMA) has validated the application for a higher dose regimen of nusinersen for spinal muscular atrophy (SMA). The higher dose regimen of nusinersen comprises a more rapid loading regimen, two 50 mg doses 14 days apart, and higher maintenance regimen, 28 mg, every 4 months, compared to the approved nusinersen regimen (SPINRAZA®).
• On April 2024, Hoffmann-La Roche announced a Phase IV Open-Label Study Evaluating the Effectiveness and Safety of Risdiplam Administered as an Early Intervention in Pediatric Patients With Spinal Muscular Atrophy After Gene Therapy
• On April 2024, Genentech announced results of a multi-center, longitudinal, prospective, non-comparative study to investigate the long-term safety and effectiveness of risdiplam, prescribed based on clinician judgment as per the Evrysdi® U.S. Package Insert (USPI) in adult and pediatric participants with spinal muscular atrophy (SMA). In this study, participants will be followed for up to 5 years from enrollment or until withdrawal of consent, loss to follow-up, or death. Participants who discontinue risdiplam may still remain in the study, if they agree to continue participating in the follow-up assessments.
• On April 2024, Biogen announced results of a study whose primary objective is to examine the clinical efficacy of nusinersen administered intrathecally at higher doses to participants with spinal muscular atrophy (SMA), as measured by change in Children’s Hospital of Philadelphia-Infant Test of Neuromuscular Disorders (CHOP-INTEND) total score (Part B); to examine the safety and tolerability of nusinersen administered intrathecally at higher doses to participants with SMA (Parts A and C).
• On January 2024, Novartis announced results of a Phase IIIb, Open-label, Single-arm, Multi-center Study to Evaluate the Safety, Tolerability and Efficacy of OAV101 Administered Intrathecally (1.2 x 10^14 Vector Genomes) to Participants 2 to < 18 Years of Age With Spinal Muscular Atrophy (SMA) Who Have Discontinued Treatment With Nusinersen (Spinraza®) or Risdiplam (Evrysdi®).
• On January 2024, NMD Pharma A/S announced results of a Phase 2, Randomised, Double-blind, Placebo-controlled, 2-way Crossover Study to Evaluate the Efficacy, Safety, and Tolerability of NMD670 in Ambulatory Adults With Type 3 Spinal Muscular Atrophy
• On December 2023, Novartis announced results of a Long-term Safety Study in Brazilian Patients With a Confirmed Diagnosis of Spinal Muscular Atrophy (SMA) Treated With Onasemnogene Abeparvovec (Zolgensma®) – ARISER Study.
• On May 2023, Biogen announced results of a study whose primary objective is to describe the natural history and utilization of disease modifying therapy (DMT) among adult Chinese participants with SMA linked to chromosome 5q (5q-SMA)

To know in detail about the Spinal Muscular Atrophy clinical trials and recent FDA approvals for Spinal Muscular Atrophy drugs, click here: Spinal Muscular Atrophy Drugs and Therapies

Spinal Muscular Atrophy Overview

Spinal Muscular Atrophy (SMA) is a rare genetic neuromuscular disorder that affects motor neurons in the spinal cord, leading to progressive muscle weakness and atrophy. It is caused by mutations in the SMN1 (Survival Motor Neuron 1) gene, which results in reduced levels of the SMN protein essential for motor neuron survival. The severity of SMA varies, and it is classified into different types (SMA 0–4) based on age of onset and disease progression.

Spinal Muscular Atrophy primarily affects voluntary muscles, particularly those involved in movement, breathing, and swallowing. Spinal Muscular Atrophy Symptoms range from severe muscle weakness in infancy (SMA Type 1, the most common and severe form) to milder symptoms with later onset (SMA Type 3 and 4). In severe cases, respiratory complications can be life-threatening.

Spinal Muscular Atrophy Diagnosis is confirmed through genetic testing. While there is no cure, disease-modifying therapies like nusinersen (Spinraza), risdiplam (Evrysdi), and gene therapy with onasemnogene abeparvovec (Zolgensma) can improve motor function and survival. Supportive care, including physical therapy, respiratory support, and nutritional management, plays a crucial role in improving the quality of life.

Spinal Muscular Atrophy Advancements in treatment and early intervention, especially through newborn screening, have significantly improved outcomes for individuals with SMA.

Spinal Muscular Atrophy Pipeline Therapeutics Assessment

• Spinal Muscular Atrophy Assessment by Product Type
• Spinal Muscular Atrophy By Stage and Product Type
• Spinal Muscular Atrophy Assessment by Route of Administration
• Spinal Muscular Atrophy By Stage and Route of Administration
• Spinal Muscular Atrophy Assessment by Molecule Type
• Spinal Muscular Atrophy by Stage and Molecule Type

DelveInsight’s Spinal Muscular Atrophy Report covers around 20+ 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

Emerging Spinal Muscular Atrophy Drugs Under Different Phases of Clinical Development Include:

• ACTX-401: Novartis
• Apitegromab: Scholar Rock
• GYM329: Roche
• And Many Others

Get a Free Sample PDF Report to know more about Spinal Muscular Atrophy Pipeline Assessment- Spinal Muscular Atrophy Medication

Spinal Muscular Atrophy Pipeline Analysis:

• The Spinal Muscular Atrophy pipeline report provides insights into
• The report provides detailed insights about companies that are developing therapies for the Spinal Muscular Atrophy treatment 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 Spinal Muscular Atrophy Treatment.
• Spinal Muscular Atrophy key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
• Spinal Muscular Atrophy 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 Spinal Muscular Atrophy 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.

Further Spinal Muscular Atrophy product details are provided in the report. Download the Spinal Muscular Atrophy pipeline report to learn more about the emerging Spinal Muscular Atrophy therapies @ Spinal Muscular Atrophy Companies and Drugs

Scope of Spinal Muscular Atrophy Pipeline Drug Insight

• Coverage: Global
• Key Spinal Muscular Atrophy Companies: Scholar Rock, Biogen, Astellas Pharma, Alcyone Therapeutics, AndroScience Corporation, Hanugen Theraputics, Voyager Therapeutics, Hoffmann-La Roche, Catalyst Pharmaceuticals, NMD Pharma, Biohaven Pharmaceuticals, CANbridge Pharmaceuticals Inc., Aurimed Pharma, Exicure, Amylon Therapeutics, Amniotics, and others
• Key Spinal Muscular Atrophy Therapies: AS-202, HK001, Tegoprubart, AP-101, BLZ945, ANX005, MN-166, TW001, BIIB067, and others
• Spinal Muscular Atrophy Therapeutic Assessment: Spinal Muscular Atrophy current marketed and Spinal Muscular Atrophy emerging therapies
• Spinal Muscular Atrophy Market Dynamics: Spinal Muscular Atrophy market drivers and Spinal Muscular Atrophy market barriers

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Table of Contents

• Spinal Muscular Atrophy Report Introduction
• Spinal Muscular Atrophy Executive Summary
• Spinal Muscular Atrophy Overview
• Spinal Muscular Atrophy- Analytical Perspective In-depth Commercial Assessment
• Spinal Muscular Atrophy Pipeline Therapeutics
• Spinal Muscular Atrophy Late Stage Products (Phase II/III)
• Spinal Muscular Atrophy Mid Stage Products (Phase II)
• Spinal Muscular Atrophy Early Stage Products (Phase I)
• Spinal Muscular Atrophy Preclinical Stage Products
• Spinal Muscular Atrophy Therapeutics Assessment
• Spinal Muscular Atrophy Inactive Products
• Company-University Collaborations (Licensing/Partnering) Analysis
• Spinal Muscular Atrophy Key Companies
• Spinal Muscular Atrophy Key Products
• Spinal Muscular Atrophy Unmet Needs
• Spinal Muscular Atrophy Market Drivers and Barriers
• Spinal Muscular Atrophy Future Perspectives and Conclusion
• Spinal Muscular Atrophy Analyst Views
• Appendix
• About DelveInsight

About DelveInsight

DelveInsight is a leading Business Consultant, and Market Research firm focused exclusively on life sciences.

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“Binge eating disorder Treatment Market”

(Albany, USA) DelveInsight’s Binge Eating Disorder Market Insights report includes a comprehensive understanding of current treatment practices, binge eating disorder emerging drugs, market share of individual therapies, and current and forecasted market size from 2020 to 2034, segmented into 7MM [the United States, the EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan].

The Binge eating disorder market report provides current treatment practices, emerging drugs, the market share of the individual therapies, and the current and forecasted Binge eating disorder market size from 2020 to 2034, segmented by seven major markets. The Report also covers current Binge eating disorder treatment practice/algorithm, market drivers, market barriers, and unmet medical needs to curate the best opportunities and assesses the underlying potential of the Binge eating disorder market.

Request for sample report @ Binge Eating Disorder Market Insights

Key Takeaways from the Binge Eating Disorder Market Report

• According to DelveInsight’s analysis, the market size for binge eating disorder is expected to grow significantly by 2034.
• Binge eating disorder is the most common eating disorder in the United States, and it affects people of all racial and ethnic groups. About 1.25% of adult women and 0.42% of adult men have binge eating disorder.
• Leading binge eating disorder companies such as TRYP Therapeutics, Tonix Pharmaceuticals, Alvogen Iceland ehf, Bausch Health Companies Inc., Chronos Therapeutics Ltd., Currax Pharmaceuticals LLC, Eli Lilly and Co., Johnson and Johnson Services Inc., Lupin Ltd., Omeros Corp., Pyramid Healthcare Inc., Rosewood Centers for Eating disorders, Sumitomo Pharma Co. Ltd., Takeda Pharmaceutical Co. Ltd., Timberline Knolls Residential Treatment Center, Tonix Pharmaceuticals Holding Corp., Tryp Therapeutics Inc., Viatris Inc., VIVUS LLC, Walden Behavioral Care and others are developing novel binge eating disorder drugs that can be available in the binge eating disorder market in the coming years.
• The promising binge eating disorder therapies in the pipeline include TRYP-0082, TNX-1900, VYVANSE (lisdexamfetamine), among others.
• In March 2025, Axsome Therapeutics, Inc announced an Open-Label Study to Assess the Long-term Safety and Efficacy of Solriamfetol in Adults with Binge Eating Disorder
• On January 30, 2025, Granules India Limited (NSE:GRAN) announced the U.S. Food & Drug Administration (FDA) approval for its generic Lisdexamfetamine Dimesylate Capsules. Available in various strengths (10 mg to 70 mg), this drug is bioequivalent to Vyvanse Capsules and is indicated for treating Attention Deficit Hyperactivity Disorder (ADHD) in both adults and children six years and older, as well as for Moderate to Severe Binge Eating Disorder (BED) in adults.
• In January 2025, Axsome Therapeutics, Inc announced a Phase 3, Randomized, Double-blind, Placebo-Controlled Trial of Solriamfetol in Adults With Binge Eating Disorder (BED)

Discover which therapies are expected to grab the major binge eating disorder market share @ Binge Eating Disorder Market Report

Binge Eating Disorder Overview

Binge eating disorder is a serious mental health condition characterized by recurrent episodes of consuming large quantities of food in a short period while feeling a loss of control over eating behavior. Unlike bulimia nervosa, individuals with binge eating disorder typically do not engage in compensatory behaviors such as purging or excessive exercise to counteract the binge eating episodes. Several factors contribute to the development of binge eating disorder, including genetic predisposition, psychological factors like stress or low self-esteem, and environmental influences such as societal pressure to attain certain body ideals. Traumatic life events, childhood experiences, and dysfunctional family dynamics may also play a role in its onset.

Symptoms of binge eating disorder include eating unusually large amounts of food in a specific time frame, eating rapidly until feeling uncomfortably full, eating alone due to embarrassment over food intake, and experiencing feelings of guilt, shame, or distress after binge eating episodes. Individuals with BED often struggle with emotional regulation and may use food as a coping mechanism to deal with stress, anxiety, or depression. Diagnosing binge eating disorder involves a comprehensive assessment by a healthcare professional, including a physical examination, psychological evaluation, and discussion of eating habits and behaviors. Criteria outlined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) are used to determine if someone meets the diagnostic criteria for BED.

Binge Eating Disorder Epidemiology Segmentation

The binge eating disorder epidemiology section provides insights into the historical and current binge eating disorder patient pool and forecasted trends for the 7MM. It helps recognize the causes of current and forecasted patient trends by exploring numerous studies and views of key opinion leaders.

The binge eating disorder market report proffers epidemiological analysis for the study period 2020–2034 in the 7MM segmented into:

• Total Prevalent Cases of Binge Eating Disorder
• Total Diagnosed Prevalent Cases of Binge Eating Disorder
• Gender-specific Diagnosed Prevalent Cases of Binge Eating Disorder
• Treatable Cases of Binge Eating Disorder

Binge Eating Disorder Treatment Market

Treatment for binge eating disorder is centered around tackling the intricate issues linked with repeated episodes of overeating, often marked by a feeling of being unable to control one’s eating habits. Therapeutic strategies, like cognitive-behavioral therapy (CBT) or dialectical behavior therapy (DBT), are commonly utilized to address the underlying emotional and psychological aspects. Additionally, nutritional guidance and encouragement are offered to encourage healthier eating habits, while medication, such as selective serotonin reuptake inhibitors (SSRIs), may be prescribed in certain instances. The primary objective is to assist individuals in managing their binge eating tendencies, enhancing their emotional state, and establishing sustainable lifestyle adjustments to facilitate long-lasting recovery.

Vyvanse (lisdexamfetamine) is the only medication approved by the FDA specifically for addressing binge eating disorders. Operating as a precursor to amphetamine, Vyvanse boosts neurotransmitter levels such as dopamine and norepinephrine in the brain, affecting impulse control and appetite management. Clinical studies have validated its effectiveness in diminishing binge eating occurrences and ameliorating associated psychological symptoms. Nonetheless, Vyvanse carries potential side effects like sleeplessness, heightened heart rate, and anxiety. Its prescription is typically reserved for situations where psychotherapy alone might not suffice, underscoring the importance of a holistic approach to treating binge eating disorder that integrates both pharmaceutical and therapeutic measures.

Fluoxetine, categorized as a selective serotonin reuptake inhibitor (SSRI), isn’t directly endorsed by the FDA for treating binge eating disorders, yet it has demonstrated effectiveness in certain instances. Despite not being formally approved for this purpose, fluoxetine is sometimes prescribed off-label to tackle the emotional and psychological aspects linked with binge eating. Through elevating serotonin levels in the brain, fluoxetine potentially aids in mood regulation and diminishing the occurrence of binge eating episodes. However, its efficacy can differ from person to person.

To know more about binge eating disorder treatment guidelines, visit @ Binge Eating Disorder Management

Binge Eating Disorder Pipeline Therapies and Key Companies

Some of the drugs in the pipeline include TRYP-0082 (TRYP Therapeutics), and TNX-1900 (Tonix Pharmaceuticals), among others.

Psilocybin (TRP-8802) signifies a groundbreaking advancement in pharmaceuticals, being developed to address various conditions such as fibromyalgia, binge eating disorder, irritable bowel syndrome (IBS), hypothalamic obesity, and chronic pain. It is administered orally in capsule form and intravenously, drawing attention to its potential to tackle a wide range of medical issues. The oral method offers convenient dosing for patients, while the intravenous route ensures precise and rapid therapeutic effects. With its unique psychedelic properties, Psilocybin presents a novel approach to treating historically difficult-to-manage disorders. Currently, the drug is undergoing Phase II clinical trials for further evaluation.

Tonix Pharmaceuticals is progressing with the development of TNX-1900, a nasal oxytocin compound enhanced for effectiveness. This medication is aimed at treating chronic migraine and binge eating disorders associated with obesity. Acquired from Trigemina, Inc., and licensed from Stanford University in 2020, the formula includes magnesium to boost oxytocin’s interaction with its receptors. Having received FDA Investigational New Drug (IND) clearance in the fourth quarter of 2021, Tonix initiated a Phase II clinical trial for BED in partnership with Massachusetts General Hospital. This trial began in March 2022 and is expected to wrap up by April 2024. It’s worth noting that Tonix Pharmaceuticals does not possess an IND for BED. Currently, the drug is undergoing Phase IIA trials for binge eating disorder treatment.

The anticipated launch of these emerging therapies for binge eating disorder are poised to transform the market landscape in the coming years. As these cutting-edge therapies continue to mature and gain regulatory approval, they are expected to reshape the binge eating disorder market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth.

Learn more about the FDA-approved drugs for binge eating disorder @ Drugs for Binge Eating Disorder Treatment

Binge Eating Disorder Market Dynamics

The dynamics of the binge eating disorder market are expected to change in the coming years. As societal understanding evolves, coupled with advances in research and healthcare, there’s a notable shift towards integrated approaches that encompass pharmacological interventions, psychotherapy, and lifestyle modifications. Pharmaceutical companies are responding with innovative drug therapies tailored to address the underlying neurobiological mechanisms of binge eating disorder, while mental health professionals are emphasizing the importance of holistic treatment models to address both physical and psychological aspects. Moreover, the rise of telemedicine and digital health platforms is expanding access to care, allowing individuals to seek support and guidance conveniently.

Furthermore, many potential therapies are being investigated for the treatment of binge eating disorder, and it is safe to predict that the treatment space will significantly impact the binge eating disorder market during the forecast period. Moreover, the anticipated introduction of emerging therapies with improved efficacy and a further improvement in the diagnosis rate are expected to drive the growth of the binge eating disorder market in the 7MM.

However several factors may impede the growth of the binge eating disorder market. One prominent barrier is the stigma surrounding mental health issues, including misconceptions about binge eating disorder as a lack of willpower rather than a complex psychological disorder. This stigma can prevent individuals from seeking help or disclosing their struggles, leading to underdiagnosis and undertreatment. Additionally, limited awareness among healthcare providers and the general public about binge eating disorder as a distinct disorder further exacerbates these challenges. Furthermore, access to specialized treatment options and binge eating disorder trained in managing binge eating disorders remains limited in many regions, hindering timely intervention and support for affected individuals.

Moreover, binge eating disorder treatment poses a significant economic burden and disrupts patients’ overall well-being and QOL. Furthermore, the binge eating disorder market growth may be offset by failures and discontinuation of emerging therapies, unaffordable pricing, market access and reimbursement issues, and a shortage of healthcare specialists. In addition, the undiagnosed, unreported cases and the unawareness about the disease may also impact the binge eating disorder market growth.

Scope of the Binge Eating Disorder Market Report

• Study Period: 2020–2034
• Coverage: 7MM [the United States, the EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan].
• Key Binge Eating Disorder Companies: TRYP Therapeutics, Tonix Pharmaceuticals, and others
• Key Pipeline Binge Eating Disorder Therapies: TRYP-0082, TNX-1900, and others
• Therapeutic Assessment: Binge Eating Disorder current marketed and emerging therapies
• Binge Eating Disorder Market Dynamics: Key Market Forecast Assumptions of Emerging Binge Eating Disorder Drugs and Market Outlook
• Competitive Intelligence Analysis: SWOT analysis and Market entry strategies
• Unmet Needs, KOL’s views, Analyst’s views, Binge Eating Disorder Market Access and Reimbursement

Discover more about binge eating disorder drugs in development @ Binge Eating Disorder Clinical Trials

Table of Contents

1. Binge Eating Disorder Key Insights

2. Binge Eating Disorder Report Introduction

3. Binge Eating Disorder Overview at a Glance

4. Binge Eating Disorder Executive Summary

5 Binge Eating Disorder Key Events

6 Epidemiology and Market Forecast Methodology

6. Disease Background and Overview

7. Binge Eating Disorder Treatment and Management

8. Binge Eating Disorder Guidelines

9. Binge Eating Disorder Epidemiology and Patient Population

10. Patient Journey

11. Key Endpoints in Binge Eating Disorder

12. Binge Eating Disorder Marketed Drugs

13. Binge Eating Disorder Emerging Drugs

14. 7MM Binge Eating Disorder Market Analysis

15. Market Access and Reimbursement

16. KOL Views

17. Unmet Needs

18. SWOT Analysis

19. Appendix

20. DelveInsight Capabilities

21. Disclaimer

22. About DelveInsight

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: Ankit Nigam
Email: Send Email
Phone: +14699457679
Address:304 S. Jones Blvd #2432
City: Albany
State: New York
Country: United States
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To view the original version on ABNewswire visit: Binge eating disorder Treatment Market 2034: Clinical Trials, EMA, PDMA, FDA Approvals, Medication, Epidemiology, Statistics, Revenue, Therapies, Treatment, Companies by DelveInsight