PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1939680
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1939680
The gastrointestinal therapeutics market is expected to grow from USD 41.94 billion in 2025 to USD 43.74 billion in 2026 and is forecast to reach USD 53.96 billion by 2031 at 4.29% CAGR over 2026-2031.

Robust demand stems from a rising digestive-disease burden, widening adoption of biologics and biosimilars, and continuous investment in microbiome-based pipelines. Specialist shortages in many countries, especially rural regions, intensify reliance on telehealth and AI-guided diagnostic tools, while regulatory support for biosimilar interchangeability accelerates price competition. Companies that combine advanced drug platforms with digital health services strengthen market access, and large-volume subcutaneous delivery systems position injectables as a viable alternative to traditional oral therapies. Meanwhile, regional expansion in Asia-Pacific, driven by healthcare infrastructure upgrades and dietary westernization, offsets pricing pressure in North America and Europe, making the gastrointestinal therapeutics market an attractive long-term play for diversified portfolios.
Colorectal-cancer screening age was lowered to 45 years in the United States, adding millions of procedures annually and amplifying demand for both diagnostics and follow-up therapeutics. Rising incidence of inflammatory bowel disease in rapidly urbanizing Asian populations underscores the need for advanced biologics that surpass acid-suppression drugs in efficacy. Expanded national screening programs in China and India funnel more patients into treatment pathways, and this earlier detection improves long-term therapeutic adherence. Government reimbursement for preventive colonoscopy further buttresses prescription volumes for antispasmodics and prokinetic agents. Collectively, these factors lift the gastrointestinal therapeutics market by enlarging the treated-patient pool and extending treatment durations.
Japan already records 29.1% of its citizens aged >=65 years, and similar trajectories in Europe and North America increase chronic proton-pump-inhibitor use for reflux management. Sedentary behavior and processed-food consumption heighten functional gastrointestinal disorders, prompting broader uptake of prokinetics and microbiome modulators. Obesity magnifies gastroesophageal reflux disease prevalence, feeding sustained PPI prescriptions despite generic erosion. Lifestyle-induced stress links to irritable bowel syndrome, reinforcing demand for low-dose antidepressant adjuncts and antispasmodics. Overall, demographic and behavioral convergence lengthens therapy courses, driving stable revenue streams in the gastrointestinal therapeutics market.
Annual biologic treatment can exceed USD 50,000, straining public and private payers that increasingly impose prior-authorization hurdles. Value-based contracts tie reimbursement to real-world outcomes, compelling manufacturers to fund post-marketing studies. Specialty pharmacies consolidate to negotiate steeper discounts, eroding gross margins yet expanding patient reach through copay-assistance programs. Emerging-market governments explore pooled procurement to lower unit prices, but constrained budgets delay biologic uptake compared with small-molecule alternatives. Although biosimilars promise relief, originators often counter with life-cycle-management strategies such as high-concentration formulations, prolonging price rigidity.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Proton pump inhibitors remained the revenue anchor in 2025, holding 23.78% gastrointestinal therapeutics market share, underpinned by widespread management of gastroesophageal reflux disease and ulcer prophylaxis. Branded PPIs still command premiums in hospital formularies where rapid-acting IV formulations are required for acute bleeding, though generics dominate retail channels. The gastrointestinal therapeutics market size attributable to PPIs is expected to plateau as guideline revisions advocate step-down therapy to minimize long-term adverse effects. In parallel, the biologics segment captures incremental spend through anti-TNF agents, IL-12/23 inhibitors, and JAK inhibitors, but faces biosimilar erosion post-2025. Antibiotics, led by rifaximin, retain niche applications in hepatic encephalopathy and small-intestinal bacterial overgrowth, aided by label expansions.
Microbiome-based therapies comprise the fastest-growing drug class at a 4.33% CAGR, albeit from a low base, benefiting from VOWST's commercial traction and promising pipelines like SER-155 for immunocompromised hosts. Live biotherapeutic product standardization and scalable anaerobic manufacturing processes cut production costs, narrowing the price gap with conventional biologics. Pharma-food cross-sector collaborations, as exemplified by Nestle Health Science, infuse diet-adjacent capabilities such as prebiotic adjuncts that enhance colonization. Over the forecast period, the gastrointestinal therapeutics market size for microbiome products is expected to expand as payers accept real-world evidence of relapse reduction in recurrent C. difficile infection.
The Gastrointestinal Therapeutics Market Report is Segmented by Drug Class (Proton Pump Inhibitors, H2 Receptor Antagonists, and More), Disease Indication (GERD, Peptic Ulcer and More), Route of Administration (Oral, Injectable, and More), Distribution Channel (Hospital Pharmacies, Retail Pharmacies, and More), and Geography (North America, Europe, and More). The Market Forecasts are Provided in Terms of Value (USD).
North America delivered 38.61% of global revenue in 2025, propelled by high biologic penetration and supportive reimbursement environments despite pronounced specialist shortages across 69.3% of counties. Tele-gastroenterology networks and capsule endoscopy interpretation centers extend reach, but the backlog for elective colonoscopy still stretches clinician capacity. Biosimilar adoption accelerates after updated interchangeability rules, with payer formularies quickly prioritizing cost-saving options.
Asia-Pacific is the fastest-growing region at a 5.12% CAGR as aging demographics in China and India intersect with government insurance expansion. Urban dietary shifts drive ulcerative colitis and Crohn's disease incidence, steering investment toward biologics manufacturing facilities in Singapore and South Korea. Meanwhile, Japan's super-aged society sustains steady demand for PPIs and prokinetics, although strict HTA controls temper price inflation. Digital-health startups capitalize on smartphone penetration to deliver microbiome-tracking apps, integrating seamlessly with hospital EMR systems to guide personalized therapy.
Europe maintains a balanced outlook, with Germany, the United Kingdom, and France jointly accounting for more than half of regional sales. HTA bodies negotiate aggressive price caps, spurring rapid biosimilar uptake that broadens patient access yet compresses margins. Southern European countries are exploring outcome-based payment models for high-cost biologics, mirroring pilot programs in Scandinavia. In South America and the Middle East & Africa, Brazil and Saudi Arabia spearhead adoption of endoscopy capital equipment and biologics, leveraging public-private partnerships to upgrade hospital infrastructure. Nonetheless, payer fragmentation and import tariffs slow widespread uptake, keeping these regions at an earlier stage of the gastrointestinal therapeutics market development curve.