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Irritable bowel syndrome (IBS) is a chronic gastrointestinal disorder characterized by abdominal pain, bloating, and altered bowel habits. As per Ashwin Porwal et al., 2024, it affects around 4% of the global population, with only about 30% of affected individuals seeking medical help. The growing focus on improving patient outcomes is driving advancements in irritable bowel syndrome therapeutic products. Emerging therapies target gut-brain interaction, microbiota modulation, and visceral hypersensitivity. According to the irritable bowel syndrome pipeline analysis by Expert Market Research, the treatment pipeline is expected to witness significant growth in the coming years, supported by ongoing R&D and rising awareness.
Major companies involved in the irritable bowel syndrome pipeline analysis include Guangzhou Zhiyi Biotechnology Co., Ltd., and TRYP Therapeutics, among others.
Leading drugs currently in the pipeline include Tenapanor, CIN-103, EBX-102-02, and others.
The pipeline growth in irritable bowel syndrome drugs is driven by rising disease prevalence, increased R&D in gut-brain axis modulation, and expanding biologic and microbiome-targeted therapies.
The Irritable Bowel Syndrome Pipeline Analysis Report by Expert Market Research gives comprehensive insights into irritable bowel syndrome therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for irritable bowel syndrome. The irritable bowel syndrome report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The irritable bowel syndrome pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with irritable bowel syndrome treatment guidelines to ensure optimal care practices.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to irritable bowel syndrome.

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Irritable bowel syndrome (IBS) is a functional gastrointestinal disorder characterized by abdominal pain, bloating, and altered bowel habits, such as diarrhea, constipation, or both. It occurs due to abnormal gut-brain interactions, visceral hypersensitivity, and changes in gut motility and microbiota, often triggered by stress, infections, or dietary factors.
Irritable bowel syndrome treatment includes dietary changes, stress management, and medications such as antispasmodics, laxatives, and selective drugs based on symptoms, especially for IBS with constipation or diarrhea. In July 2022, the American Gastroenterological Association recommended linaclotide, plecanatide, and lubiprostone as pharmacological treatments in the irritable bowel syndrome with constipation (IBS-C) drug pipeline, improving fluid secretion and easing bowel movements.
According to Chaoping Li et al., 2024, irritable bowel syndrome (IBS) affects 7%-21% of the global population, with an estimated adult prevalence of 8.8%. In Asia, the rate is higher at 12.6%. According to Ashwin Porwal et al., 2024, IBS is more common in females and individuals under 50 years of age. The incidence rates vary in different countries, with factors such as dietary habits, lifestyle, and healthcare access. Only about 30% of those experiencing symptoms seek medical attention, indicating underdiagnosis and unmet treatment needs.
This section of the report covers the analysis of irritable bowel syndrome drug candidates based on several segmentations, including:
By Phase
By Drug Class
By Route of Administration
The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II (accounts for 38%) covers a major share of the total irritable bowel syndrome clinical trials, highlighting strong mid-stage clinical activity. Phase III represents 29%, indicating significant progress toward regulatory approval. Phase I and phase IV each contribute 12.5%. This balanced development pipeline can accelerate innovative treatment availability, positively impacting market growth and patient outcomes.
The drug molecule categories covered under the irritable bowel syndrome pipeline analysis include small molecules, monoclonal antibodies, peptides, polymers, and gene therapies. The irritable bowel syndrome report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for irritable bowel syndrome. Serotonergic agents are emerging as promising candidates in the treatment pipeline for irritable bowel syndrome (IBS). For instance, LX1031, a tryptophan hydroxylase inhibitor, is under clinical evaluation. It targets serotonin production in the gastrointestinal tract to reduce abdominal pain and regulate bowel habits, offering a novel mechanism for managing non-constipation predominant IBS symptoms.
The EMR report for the irritable bowel syndrome pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a detailed irritable bowel syndrome therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in irritable bowel syndrome clinical trials:
This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for irritable bowel syndrome. It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of irritable bowel syndrome drug candidates.
Tenapanor is currently being evaluated in a Phase 3 open-label long-term safety study sponsored by Ardelyx for pediatric patients aged 6 to less than 18 years with IBS-C (irritable bowel syndrome with constipation). The objective of this phase is to examine the long-term safety and tolerability of tenapanor.
CIN-103, developed by CinPhloro Pharma, LLC, is currently being evaluated in a Phase 2 clinical trial for adults with irritable bowel syndrome with predominant diarrhea (IBS-D). This study is assessing the efficacy, safety, and tolerability of CIN-103, a non-opioid small molecule formulation of phloroglucinol targeting motility, secretion, pain, spasms, and inflammation. Researchers are comparing two dose strengths of CIN-103 with a placebo to determine symptom improvement and tolerability.
EBX-102-02 is being sponsored by EnteroBiotix in a Phase II clinical trial to evaluate its potential for treating irritable bowel syndrome (IBS) with constipation. The study is currently assessing the safety and tolerability of this next-generation, full-spectrum microbiome drug. EBX-102-02 contains diverse microbial ecosystems using AMPLA technology, aiming to restore gut balance and improve IBS symptoms. The trial is enrolling 60 patients across UK sites.
*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*
The Irritable Bowel Syndrome Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for irritable bowel syndrome. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into irritable bowel syndrome collaborations, regulatory environments, and potential growth opportunities.
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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