DelveInsight’s, “Irritable Bowel Syndrome Pipeline Insight, 2023,” report provides comprehensive insights about 24+ companies and 24+ pipeline drugs in Irritable Bowel Syndrome pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Irritable Bowel Syndrome pipeline therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
For Irritable Bowel Syndrome Emerging drugs, the Irritable Bowel Syndrome pipeline analysis report provides a 360° view of the therapeutics landscape by development point, product type, route of administration, molecule type, and MOA. The Irritable Bowel Syndrome pipeline research covers business opportunities, challenges, future partnerships, strong competitors, and growth strategies.
In the Irritable Bowel Syndrome Pipeline Report, a detailed description of the drug is given which includes the mechanism of action of the drug, Irritable Bowel Syndrome clinical trials studies, Irritable Bowel Syndrome NDA approvals (if any), and product development activities comprising the technology, Irritable Bowel Syndrome collaborations, licensing, mergers and acquisition, funding, designations, and other product-related details.
Key takeaways from the Irritable Bowel Syndrome Pipeline Report
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Irritable Bowel Syndrome Overview
Irritable bowel syndrome (IBS) is a group of symptoms that occur together, including repeated pain in your abdomen and changes in your bowel movements, which may be diarrhea, constipation, or both. With IBS, you have these symptoms without any visible signs of damage or disease in your digestive tract. The most common symptoms of irritable bowel syndrome (IBS) are pain in your abdomen, often related to your bowel movements, and changes in your bowel movements.
Recent Developmental Activities in the Irritable Bowel Syndrome Treatment Landscape
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Irritable Bowel Syndrome Emerging Drugs Profile
ORP-101 is a new chemical entity designed to confer peripheral partial μ agonist and full κ receptor antagonist activity, enabling treatment of both IBS-D symptoms of dysmotility and pain without the risk of sphincter of Oddi spasm or pancreatitis. ORP-101 has been shown in preclinical studies to not cross the blood-brain barrier. ORP-101 successfully completed Phase 1 clinical trials and was granted FDA Fast Track designation in 2018. Regulatory path to NDA has been agreed with the FDA. Currently, it is in Phase II stage of clinical trial evaluation to treat Irritable bowel syndrome.
Blautix® is a single strain Live Biotherapeutic product (LBP), being developed as a treatment for both IBS-C and IBS-D. Pre-clinical studies demonstrated its ability to address visceral hypersensitivity and other symptoms of IBS and increase microbiome diversity. A Phase I study in healthy volunteers and IBS patients showed that Blautix® was well tolerated and an improvement in symptoms was also reported relative to placebo. The Phase II BHT-II-002 trial demonstrated an impact on overall response with regards to bowel habit and abdominal pain in IBS-C and IBS-D. Blautix® was well tolerated, with a safety profile comparable to placebo.
Irritable Bowel Syndrome Pipeline Therapeutics Assessment
There are approx. 24+ key companies which are developing the therapies for Irritable bowel syndrome. The companies which have their Irritable bowel syndrome drug candidates in the most advanced stage, i.e. phase II include OrphoMed.
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Scope of the Irritable Bowel Syndrome Pipeline Report
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Table of Content
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