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BioWorld - Wednesday, April 15, 2026
Home » Topics » Gastrointestinal, BioWorld

Gastrointestinal, BioWorld
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Liver disease

Cohbar shares climb as early NAFLD data hint at potential in NASH

Aug. 11, 2021
By Michael Fitzhugh
Shares of Cohbar Inc. (NASDAQ:CWBR) hit a 52-week high on Aug. 11 following news that a mitochondrial peptide analogue it is testing for the potential treatment of nonalcoholic steatohepatitis (NASH) and obesity, CB-4211, delivered "robust" improvements in key biomarkers of liver damage and glucose levels vs. placebo during a small phase Ia/Ib study.
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UC, it’s about the pipeline; next-gen candidate touted after Seres miss

July 22, 2021
By Randy Osborne
Differences between Seres Therapeutics Inc.’s next-generation microbiome therapy and SER-287 were highlighted in the wake of the phase IIb failure with the latter in the study called Eco-Reset, which missed its primary endpoint of improving clinical remission rates in ulcerative colitis (UC) compared to placebo.
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Vedanta’s $68M series D to bolster its human microbiome therapies

July 21, 2021
By Lee Landenberger
Proceeds from Vedanta Biosciences Inc.’s just closed $68 million series D financing will be used for a phase III study of the company’s lead candidate, VE-303, composed of eight clonal human commensal bacterial strains to give colonization resistance for treating Clostridioides difficile (C. diff) infection, and also for a phase II study of VE-202, made up of 16 clonal human commensal bacterial strains for treating inflammatory bowel disease.
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First therapy for rare liver disease PFIC, as Albireo’s Bylvay earns priority FDA nod

July 20, 2021
By Jennifer Boggs
Albireo Pharma Inc.’s Bylvay (odevixibat) becomes the first therapy to hit the commercial market for rare genetic liver disease progressive familial intrahepatic cholestasis (PFIC). A day after the European Commission approved the drug, the FDA gave the nod to the ileal bile acid transport inhibitor on its July 20 PDUFA date following a priority review.
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Hepion’s positive phase IIa NASH data disappoint the Street

July 13, 2021
By Lee Landenberger
All the primary endpoints were met in Hepion Pharmaceuticals Inc.’s phase IIa trial of CRV-431 for treating nonalcoholic steatohepatitis (NASH). The market, however, wasn’t celebrating as the Edison, N.J.-based company’s stock (NASDAQ:HEPA) sagged 15.27% on July 13 to close at $1.72 per share.
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Hightide’s HTD-1801 meets primary endpoint in phase II trial for PSC

June 30, 2021
By Elise Mak
Hightide Therapeutics Inc. presented top-line results of its lead program, HTD-1801, from a multicenter phase II trial in primary sclerosing cholangitis (PSC), which showed the drug candidate reduced alkaline phosphatase levels compared to placebo.
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Conference data for June 28, 2021: EASL

June 28, 2021
New and updated preclinical and clinical data presented by biopharma firms at The International Liver Congress – The Annual Meeting of the European Association for the Study of the Liver, including: Arbutus, Arrowhead.
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Conference data for June 23, 2021: EASL

June 23, 2021
New and updated preclinical and clinical data presented by biopharma firms at The International Liver Congress – The Annual Meeting of the European Association for the Study of the Liver, including: Antios, Arrowhead, Assembly, Brii, Durect, Enanta, Mirum.
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Ochre Bio co-founders Jack O’Meara and Quin Wills

Ochre Bio closes $10M seed round to map and drug the liver

June 16, 2021
By Cormac Sheridan
DUBLIN – Ochre Bio Ltd. has raised $9.6 million in seed financing to drug the liver like never before, by combining genetics, single-cell genomics, spatial sequencing, imaging and machine learning to build a high-resolution, in silico model of the organ, which can provide new insights into disease biology and open up new drug targets.
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Alentis’ $67M series B to advance Claudin-1-targeting antibody into clinic

June 15, 2021
By Nuala Moran
LONDON – Alentis Therapeutics SA is now equipped to deliver initial proof of concept for its universal approach to treating fibrosis, after raising $67 million in an oversubscribed series B.
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