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BioWorld - Friday, February 13, 2026
Home » Topics » Disease categories and therapies » Gastrointestinal

Gastrointestinal
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Gastrointestinal

PDE4 prodrug exhibits colon-selective bioactivation in colitis models

Jan. 30, 2024
Phosphodiesterase-4 (PDE4) is an intracellular pro-inflammatory enzyme that is considered a therapeutic target in inflammatory disorders such as psoriasis, asthma or ulcerative colitis (UC), among others. Researchers from Palisade Bio Inc. have reported preclinical data on PALI-2108, a PDE4 inhibitor prodrug, in models of UC.
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Dupixent

US FDA clears Dupixent for children with eosinophilic esophagitis

Jan. 26, 2024
By Karen Carey
Becoming the first treatment for children ages 1 to 11 with eosinophilic esophagitis (EE), Sanofi SA and Regeneron Pharmaceuticals Inc.’s IL-4/IL-13 inhibitor Dupixent (dupilumab) was cleared by the U.S. FDA on Jan. 25.
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Liver illustration

Sagimet soars with phase IIb NASH data

Jan. 22, 2024
By Lee Landenberger
Sagimet Biosciences Inc. stock (NASDAQ:SGMT) more than doubled Jan. 22 as shares closed 170% higher at $18.42 each as a phase IIb study of lead candidate denifanstat performed well against nonalcoholic steatohepatitis (NASH) compared to placebo. Top-line data from the 52-week, randomized, double-blind Fascinate-2 trial showed the oral fatty acid synthase inhibitor resulted in statistically significant improvements in biopsy-confirmed NASH patients with stage 2 or stage 3 fibrosis, which is moderate to severe disease, at week 52.
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Gastrointestinal

Astrazeneca divulges new FAPα inhibitors for NASH

Jan. 16, 2024
Astrazeneca AB has synthesized fibroblast activation protein-α (FAPα) inhibitors reported to be useful for the treatment of nonalcoholic steatohepatitis (NASH), among others.
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Liver illustration
Gastrointestinal

V1A agonist PHIN-214 shows promise for cirrhosis-associated portal hypertension

Jan. 16, 2024
There are several factors that induce cirrhosis. During cirrhosis, there is an increased intrahepatic resistance to blood flow, leading to portal hypertension, among others, where portal vein pressure is increased.
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Villi in intestinal tract.
Immuno-oncology

Targeting CTLA-4 without colitis induction is gut microbiota dependent

Jan. 16, 2024
By Xavier Bofill Bruna
Immune checkpoint inhibitors (ICIs), such as anti-CTLA-4 antibodies, are widely used in cancer immunotherapy. CTLA-4 blockers such as Yervoy (ipilimumab, Bristol Myers Squibb Co.) stimulate antitumoral immune responses, but may also induce toxicity, such as colitis, a common immune-related adverse event that can lead to treatment discontinuation.
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Gastrointestinal

Pterostilbene derivative shows activity in colitis model

Jan. 15, 2024
Researchers from Hefei University and Anhui Medical University have reported the discovery of novel nitric oxide (NO) inhibitors as anti-inflammatory agents for the treatment of acute colitis.
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Gastrointestinal system with ulcerative colitis.
Gastrointestinal

NLRP3 inhibitor’s efficacy and safety demonstrated in colitis models

Jan. 10, 2024
Inflammasomes are essential components of the innate immune system with a multiprotein structure.
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siRNA bound to mRNA

Boehringer strikes deals with Ribo, 3T Biosciences with combined $2.5B value

Jan. 9, 2024
By Tamra Sami
Boehringer Ingelheim GmbH’s start to the new year includes two fresh deals across two continents. BI struck one deal with Kunshan, China-based Suzhou Ribo Life Science Co. Ltd. and its Mölndal, Sweden-based subsidiary, Ribocure Pharmaceuticals AB, to develop small interfering RNA (siRNA) treatments for nonalcoholic or metabolic dysfunction-associated steatohepatitis. It struck a second deal with San Francisco-based 3T Biosciences Inc. to develop cancer immunotherapies, which builds on an earlier collaboration formed last year. Combined, the two deals are worth more than $2.5 billion.
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Antibodies
Gastrointestinal

Characterization of DONQ-52, a multispecific antibody against HLA-DQ2.5/gluten peptide complexes

Jan. 9, 2024
Patients with celiac disease have gluten-specific CD4+ T cells that recognize gluten via disease-associated human leukocyte antigen (HLA) molecules, specifically HLA-DQ2.5, leading to immune activation and enteropathy.
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