Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
The intestines are a vital organ system within the gastrointestinal tract, traditionally divided into the small intestine (comprising the duodenum, jejunum, and ileum) and the large intestine (comprising the colon and rectum) [6, 10]. They perform essential biological functions including the enzymatic digestion of food, the absorption of nutrients and electrolytes, and the reabsorption of water to form solid waste [6, 11]. Beyond digestion, the intestines play a critical role in systemic immunity through the gut-associated lymphoid tissue (GALT) and serve as an endocrine organ, secreting hormones such as glucagon-like peptide-1 (GLP-1) and serotonin that regulate metabolism and motility [7, 12]. In the pharmaceutical industry, the intestines are often studied as a site for localized drug delivery to treat conditions like Inflammatory Bowel Disease (IBD) or as a physiological barrier containing transporters (e.g., P-gp, PEPT1) and enzymes (e.g., CYP3A4) that dictate the bioavailability of oral medications [6, 13]. While the term "intestines" refers to an anatomical structure rather than a discrete molecular target, it encompasses numerous specific receptors and pathways—such as Guanylate cyclase-C and the Wnt/beta-catenin signaling pathway—that are targeted to treat gastrointestinal and metabolic disorders [1, 7].
Drugs targeting the intestines act via diverse localized mechanisms, including the inhibition of pro-inflammatory cytokines such as TNF-alpha to reduce mucosal inflammation, the activation of luminal receptors like Guanylate cyclase-C to stimulate fluid secretion and intestinal transit, or the modulation of the enteric nervous system through opioid or serotonin receptor pathways [6, 12]. Additionally, some therapies target specific intestinal transporters (e.g., SGLT1 or ASBT) to manage metabolic conditions and bile acid malabsorption [1, 13].
6 more in the full profile.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on Intestine.