PUBLISHER: DelveInsight | PRODUCT CODE: 2023874
PUBLISHER: DelveInsight | PRODUCT CODE: 2023874
Short bowel syndrome (SBS) Insights and Trends
Short bowel syndrome (SBS) Market size and forecast of the 7MM
DelveInsight's 'Short bowel syndrome (SBS) - Market Insights, Epidemiology and Market Forecast - 2036' report delivers an in-depth understanding of the SBS, historical and forecasted epidemiology, as well as the SBS market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.
The SBS market report delivers a comprehensive analysis of the current treatment landscape, including standards of care, clinical practices, and evolving therapeutic algorithms. It evaluates, SBS patient burden trends, revenue & market share dynamics, peak patient share & therapy uptake analysis, and provides an in-depth market size assessment, and growth rate projections (Historical & Forecast 2022-2036) across global regions. The report highlights key unmet medical needs in SBS and maps the competitive and clinical landscape to uncover high-value opportunities, providing a clear outlook on future market growth potential.
Key Factors Driving the Short bowel syndrome (SBS) Market
SBS Overview and Diagnosis
Short bowel syndrome is a complex condition caused by the loss or dysfunction of portions of the small and/or large intestine, resulting in reduced absorption of nutrients, fluids, and electrolytes. It commonly presents with severe diarrhea, dehydration, malnutrition, and weight loss, and in some cases may become life-threatening, although it can often be managed despite having no cure. In adults, the normal small bowel length ranges from 275-850 cm, and SBS is typically defined as having less than 180-200 cm of remaining small intestine, often necessitating nutritional support. Most cases arise from major bowel resection, and prognosis largely depends on age and underlying disease, with around two-thirds of patients surviving the first year.
SBS is diagnosed through medical history, physical examination, and tests such as blood work, fecal fat analysis, and imaging, with additional procedures like endoscopy or liver biopsy to assess complications, while treatment is individualized and focuses on maintaining nutrition, promoting intestinal adaptation, and managing complications using total parenteral nutrition (TPN), enteral feeding, dietary modifications, medications, and, in severe cases, surgery or intestinal transplantation.
Current SBS Treatment Landscape
Treatment of SBS is complex and individualized, focusing on maintaining nutrition, enhancing intestinal adaptation, and managing complications through approaches such as total parenteral nutrition (TPN), enteral feeding, dietary modifications, oral rehydration, medications, and, in severe cases, surgery or intestinal transplantation. Mild cases may be managed with diet and anti-diarrheal therapy, while many patients require TPN, though newer therapies like growth hormone and GLP-2 analogs have reduced long-term dependence. Nutritional management is central, with gradual transition from TPN to enteral or oral feeding as intestinal function improves, supported by tailored diets, small frequent meals, and supplementation. Medications include anti-diarrheals, acid-suppressing agents, and absorption-enhancing drugs, with antibiotics or enzyme therapy used when needed. Surgical options, reserved for refractory cases, include bowel-lengthening procedures (e.g., STEP, Bianchi) and, in severe cases, small bowel transplantation, particularly for patients with TPN-related complications or inadequate nutritional status.
Short bowel syndrome (SBS) Unmet Needs
The section "unmet needs of SBS" outlines the critical gaps between the current state of patient care, diagnosis, and the ideal & effective management of the disease. It highlights the obstacles experienced by patients, clinicians, and researchers and identifies potential solutions for future progress.
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Key Findings from SBS Epidemiological Analysis and Forecast
Short bowel syndrome (SBS) Drug Analysis & Competitive Landscape
The SBS drug chapter provides a detailed, market-focused review of approved therapies and the emerging pipeline across Phase I-III clinical trials. It covers mechanism of action, clinical trial data, regulatory approvals, patents, collaborations, strategic partnerships upcoming Key catalyst for each therapy, along with their advantages, limitations, and recent developments. This section offers critical insights into the SBS treatment landscape, supporting market assessment, competitive analysis, and growth forecasting for the SBS market.
Approved Therapies for SBS
GATTEX/REVESTIVE (teduglutide): Takeda (Shire Pharmaceuticals)
Teduglutide is a novel, recombinant analogue of human GLP-2, a naturally occurring protein involved in the rehabilitation of the intestinal lining. It has been developed to reduce dependence on parenteral nutrition in adult patients with SBS. Teduglutide has received ODD for the treatment of SBS from the EMA and the US FDA.
Short bowel syndrome (SBS) Pipeline Analysis
Apraglutide: Ironwood Pharmaceuticals (VectivBio)
Apraglutide is an investigational, next-generation, long-acting synthetic GLP-2 analog being developed for a range of rare gastrointestinal diseases where GLP-2 can play a central role in addressing disease pathophysiology, including SBS-IF.
In August 2025, according to the Q2 2025 corporate highlights, following discussions with the US FDA in April 2025, the company is finalizing a confirmatory apraglutide Phase III trial design for patients with SBS who are dependent on parenteral support and plans to align with the FDA in Q4 of 2025. Pending alignment with the FDA, Ironwood expects to initiate a confirmatory Phase III trial in the 1H of 2026.
Glepaglutide (ZP1848): Zealand Pharma
Glepaglutide is a long-acting GLP-2 analog in development as a potential treatment option for SBS. Glepaglutide is being developed as a liquid product in an autoinjector designed for subcutaneous administration, aimed to reduce or eliminate the need for parenteral support in people living with SBS. The US FDA has granted ODD for glepaglutide for the treatment of SBS.
As per the Q2 2025 presentation in August 2025, the company had completed the Type A meeting with the US FDA, ensuring the alignment on the design of EASE-5, and anticipates the initiation of the Phase III trial (EASE-5) in H2 2025 to support resubmission in the US.
Short bowel syndrome (SBS) Key Players, Market Leaders and Emerging Companies
Short bowel syndrome (SBS) Drug Updates
The short bowel syndrome (SBS) market is evolving from reliance on total parenteral nutrition (TPN) the current cornerstone despite its cost, risks, and long-term burden toward advanced therapies that reduce dependence on parenteral support. Growing use of GLP-2 analogs such as GATTEX/REVESTIVE, along with emerging next-generation agents like apraglutide offering improved efficacy and convenient dosing, is driving this shift. With declining use of older growth hormone therapies and a strong focus on achieving intestinal autonomy, the SBS market is poised for significant growth, supported by innovation in biologics and ongoing pipeline advancements.
Drug Class/Insights into Leading Emerging and Marketed Therapies in SBS (2022-2036 Forecast)
The SBS market comprises Peptides, and others, each targeting different aspects of tumor growth and progression.
Peptide: Peptide-based therapies are emerging as innovative treatment strategies, targeting key pathways involved in intestinal adaptation and absorption to reduce dependence on parenteral nutrition and improve clinical outcomes.
Short bowel syndrome (SBS) Drug Uptake
This section focuses on the uptake rate of potential drugs expected to be launched in the market during the forecast period (2026-2036). The analysis covers the SBS drug's uptake, performance at peak, factors affecting performance during prime years of growth, patient uptake by therapy, and anticipated sales generated by each drug.
Detailed insights of emerging therapies' drug uptake is included in the report
Market Access and Reimbursement of Approved therapies in Short bowel syndrome (SBS)
The report further provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenario of approved therapies, programs making accessibility easier and out-of-pocket costs more affordable, insights on patients insured under federal or state government prescription drug programs, etc.
Reimbursement is a crucial factor that affects the drug's access to the market. Often, the decision to reimburse comes down to the price of the drug relative to the benefit it produces in treated patients. To reduce the healthcare burden of these high-cost therapies, many payment models are being considered by payers and other industry insiders.
NOTE: Further Details are provided in the final report....
SBS therapies Price Scenario & Trends
Pricing and analogue assessment of SBS therapies highlights evolving price dynamics structures. This section summarizes the cost of approved treatments, closest and most approproiate analogue selection for emerging therapies, and understanding of how pricing influences market access, adherence, and long-term uptake.
GATTEX ranked as the 11th most expensive drug in the US in 2020, with a monthly cost of approximately USD 40,450 (as of March 2020) for 30 vials. Since GATTEX is typically administered on an ongoing basis, the total cost of treatment can be difficult to define. This becomes especially relevant when patients do not show the expected clinical response; however, it is important to consider that some individuals may experience a significant delayed response even after 24 months of therapy. For our analysis, we used a 12-month treatment duration, as patients typically remain on therapy for 6 to 24 months. Based on this timeframe and standard daily subcutaneous dosing, the estimated annual cost of therapy may reach approximately USD 485,400.
Industry Experts and Physician Views for Short bowel syndrome (SBS)
To keep up with SBS market trends, we take Key Opinion Leaders (KOLs) and Subject Matter Experts (SMEs) opinions working in the domain through primary research to fill the data gaps and validate our secondary research. Industry Experts were contacted for insights on the SBS emerging therapies, evolving treatment landscape, patient adherence to conventional therapies, therapy switching trends, drug adoption and uptake, accessibility challenges, and epidemiology and real-world prescription patterns in SBS, including MD, PhD, Instructor, Postdoctoral Researcher, Professor, Researcher, and others.
DelveInsight's analysts connected with 10+ KOLs to gather insights at country level. Centers such as the University of California, Imperial College London, Hokkaido University, and Cholangiocarcinoma Foundation, etc. were contacted.Their opinion helps understand and validate current and emerging SBS therapies, highlight unmet medical needs, provide epidemiological context, and support strategic decisions for market access, therapy adoption, and pipeline prioritization in SBS.
Qualitative Analysis: SWOT and Conjoint Analysis
We perform qualitative and market Intelligence analysis using various approaches, such as SWOT analysis and conjoint analysis.
In the SWOT analysis of SBS, strengths, weaknesses, opportunities, and threats in terms of disease diagnosis, patient awareness, patient burden, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided.
Conjoint analysis analyzes emerging therapies based on relevant attributes such as safety, efficacy, frequency of administration, route of administration, and order of entry. Scoring is given based on these parameters to analyze the effectiveness of therapy.
The team of analysts analyzes promising emerging therapies based on relevant attributes such as safety, efficacy, frequency of administration, route of administration, and order of entry. In efficacy, the trial's primary and secondary outcome measures are evaluated, whereas the therapies' safety is evaluated, wherein the acceptability, tolerability, and adverse events are majorly observed. In addition, the scoring is also based on the route of administration, order of entry, probability of success, and the addressable patient pool for each therapy. According to these parameters, the final weightage score and the ranking of the emerging therapies are decided.
Market Insights