Transthera Sciences Reports Positive Phase 2 Results for Tinengotinib in Cholangiocarcinoma
TransThera Sciences (Nanjing) Inc. has announced the publication of clinical results from a US-based Phase 2 trial evaluating its core product, Tinengotinib, in patients with cholangiocarcinoma $(CCA)$. The results were published in The Lancet Gastroenterology and Hepatology. The study involved patients with FGFR2 fusion-positive CCA who had either primary or acquired resistance to prior FGFR inhibitor therapy, as well as patients with other FGFR alterations or FGFR wild-type tumors. Tinengotinib demonstrated clinical activity in patients with FGFR2 fusion-positive CCA with acquired resistance to FGFR inhibitors, as well as in other FGFR-altered subtypes. The company notes there is no assurance that Tinengotinib will ultimately be successfully developed and marketed.
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. Transthera Sciences (Nanjing) Inc. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20251217-11959013), on December 17, 2025, and is solely responsible for the information contained therein.
免責聲明：投資有風險，本文並非投資建議，以上內容不應被視為任何金融產品的購買或出售要約、建議或邀請，作者或其他用戶的任何相關討論、評論或帖子也不應被視為此類內容。本文僅供一般參考，不考慮您的個人投資目標、財務狀況或需求。TTM對信息的準確性和完整性不承擔任何責任或保證，投資者應自行研究並在投資前尋求專業建議。