Galmed Pharmaceuticals Announces Promising Preclinical Results of Aramchol in Treating PSC-Related Fibrosis, Paving Way for Future Clinical Trials

Reuters
05-13
Galmed Pharmaceuticals Announces Promising Preclinical Results of Aramchol in Treating PSC-Related Fibrosis, Paving Way for Future Clinical Trials

Galmed Pharmaceuticals Ltd. has announced promising results from pre-clinical studies of their drug Aramchol, which shows significant anti-fibrotic effects in models of primary sclerosing cholangitis $(PSC.AU)$. Aramchol, an SCD1 inhibitor, demonstrated the ability to attenuate and prevent biliary fibrosis in mouse models of PSC, significantly inhibiting TGFβ-induced hepatic fibrosis pathways and upregulating PPAR signaling. These pre-clinical findings provide a strong rationale for further clinical trials, particularly in patients suffering from fibrosis-driven liver cancers. Galmed's President and CEO, Allen Baharaff, emphasized the potential for Aramchol to advance into Phase 2/3 clinical studies, given its robust anti-fibrotic effects previously observed in clinical studies with NASH and advanced fibrosis patients. This development marks a significant step forward in addressing the urgent need for effective treatments for biliary fibrosis and related liver conditions.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Galmed Pharmaceuticals Ltd. published the original content used to generate this news brief via PR Newswire (Ref. ID: IO86582) on May 13, 2025, and is solely responsible for the information contained therein.

免责声明:投资有风险,本文并非投资建议,以上内容不应被视为任何金融产品的购买或出售要约、建议或邀请,作者或其他用户的任何相关讨论、评论或帖子也不应被视为此类内容。本文仅供一般参考,不考虑您的个人投资目标、财务状况或需求。TTM对信息的准确性和完整性不承担任何责任或保证,投资者应自行研究并在投资前寻求专业建议。

热议股票

  1. 1
     
     
     
     
  2. 2
     
     
     
     
  3. 3
     
     
     
     
  4. 4
     
     
     
     
  5. 5
     
     
     
     
  6. 6
     
     
     
     
  7. 7
     
     
     
     
  8. 8
     
     
     
     
  9. 9
     
     
     
     
  10. 10