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BioWorld - Saturday, April 4, 2026
Home » Topics » Disease categories and therapies » Gastrointestinal

Gastrointestinal
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Group photo, including Onconic CEO John Kim, at Kosdaq

Cancer, GI-focused Onconic shares take off after ₩20B IPO

Dec. 24, 2024
By Marian (YoonJee) Chu
Onconic Therapeutics Inc., a subsidiary of Jeil Pharmaceutical Co. Ltd., saw its shares (KOSDAQ:476060) ascend for two consecutive days after debuting with a ₩20.15 billion (US$13.89 million) IPO on the Korea Exchange Dec. 19. Seoul, South Korea-based Onconic’s Kosdaq IPO offered about 1.55 million shares at ₩13,000 each, which was lowered from its original price band of ₩16,000 to ₩18,000 per share after demand forecasting.
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Group photo, including Onconic CEO John Kim, at Kosdaq

Cancer, GI-focused Onconic shares take off after ₩20B IPO

Dec. 20, 2024
By Marian (YoonJee) Chu
Onconic Therapeutics Inc., a subsidiary of Jeil Pharmaceutical Co. Ltd., saw its shares (KOSDAQ:476060) ascend for two consecutive days after debuting with a ₩20.15 billion (US$13.89 million) IPO on the Korea Exchange Dec. 19. Seoul, South Korea-based Onconic’s Kosdaq IPO offered about 1.55 million shares at ₩13,000 each, which was lowered from its original price band of ₩16,000 to ₩18,000 per share after demand forecasting.
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CRL for Zealand Pharma's glepaglutide; Novo’s Cagrisema disappoints

Dec. 20, 2024
By Nuala Moran
Shares in Zealand Pharma A/S (CO:ZEAL) dropped 22.4% to as low as DKK587 (US$82.16) on Dec. 20, after the U.S. FDA issued a complete response letter (CRL) for glepaglutide in the treatment of short bowel syndrome.
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Illustration for inflammatory bowel disease

Teva-Sanofi upbeat on ‘best-in-class’ duvakitug bowel disease data

Dec. 17, 2024
By Karen Carey
The potential for TL1A-targeting duvakitug to impact unmet needs of patients with ulcerative colitis (UC) and Crohn’s disease (CD), and to provide antifibrotic effects for a host of other diseases, boosted shares of Teva Pharmaceutical Industries Ltd. and Sanofi SA by 26.5% and 6.7%, respectively, as the partners released what analysts called “best-in-class” results from the phase IIb Relieve UCCD study and prepare for a phase III trial in 2025.
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Welireg, Emcitate among drugs EMA recommends for approval

Dec. 13, 2024
By Nuala Moran
The EMA’s Committee for Medicinal Products for Human Use recommended 17 drugs for approval at its December meeting, bringing the total for 2024 to 114. That is up from the 77 drugs recommended for approval in 2023, of which 39 were novel.
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Gastrointestinal

NIDDK grant supports Orphagen’s RARα antagonist for inflammatory bowel disease

Dec. 10, 2024
Orphagen Pharmaceuticals Inc. has been granted an award of up to $1.7 million.
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Celltrion building and skyline

Celltrion to expand CRDMO business, hit ₩10T sales in 2027

Dec. 3, 2024
By Marian (YoonJee) Chu
South Korean billionaire and chairman of Celltrion Group Jungjin Seo is returning Celltrion Inc. to its contract manufacturing organization (CMO) roots, as it relies on biosimilar sales to anchor the company in a fiercely competitive novel drug R&D arena.
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Gastrointestinal

EA-3571, a dual inhibitor of enteropeptidase and trypsin with efficacy in mouse model of MASH

Dec. 3, 2024
Recently presented preclinical data show that EA Pharma Co. Ltd.'s EA-3571 is a highly potent dual inhibitor of enteropeptidase and trypsin with luminal action, resulting in potential anti-insulin resistance and fat-burning properties.
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Gastrointestinal

Amgen discloses 15-PGDH inhibitors

Dec. 3, 2024
Amgen Inc. has reported new 5,6- and 6,6-fused bicyclic alcohols and ethers acting as 15-hydroxyprostaglandin dehydrogenase (15-PGDH) inhibitors. They are reported to be useful for the treatment of gastrointestinal disorders.
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Gastrointestinal

SRT-015 prevents acute liver injury in preclinical tests

Dec. 3, 2024
Genfit SA and its collaborators have described the preclinical efficacy of SRT-015, a liver-selective ASK1 inhibitor in models of liver failure.
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