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Clinical trial · no report yet · Phase 3

FIRST-308

Study of Tinengotinib VS. Physician's Choice a Treatment of Subjects With FGFR-altered in Cholangiocarcinoma

  • NCT05948475 ↗
  • Active, not recruiting
  • TransThera Sciences (Nanjing), Inc.
  • Focused

We haven't built a report for this trial yet. This page shows the registry record and the public commentary we found that names the trial. A report reads that commentary and sets out what clinicians said about the trial, each point linked to its source. How reports are made.

Preliminary discovery

Commentary in our index that names this trial so far

Podcasts, YouTube videos and X posts we have indexed. A report screens them, searches for more and cites what clinicians said when it is built, so final coverage is set at build.

ChannelFound
X threads4
Bluesky threads1

The trial

ClinicalTrials.gov
Official title
A Phase III, Randomized, Controlled, Global Multicenter Study to Evaluate the Efficacy and Safety of Oral Tinengotinib VS Physician's Choice in Subjects With FGFR-altered, Chemotherapy- and FGFR Inhibitor-Cholangiocarcinoma
Phase
Phase 3
Status
Active, not recruiting
Conditions
Cholangiocarcinoma
Interventions
Tinengotinib 8 mg; Tinengotinib 10 mg; Physician's Choice
Arms
  • Tinengotinib 8 mg QD · Experimental
  • Tinengotinib 10 mg QD · Experimental
  • Physician's Choice · Active comparator
Enrollment
200 (estimated)
Primary outcomes
  • Part A: Incidence, duration, and severity of adverse events (AEs)
  • Part B: PFS by BICR
Sponsor
TransThera Sciences (Nanjing), Inc.
Start
Dec 20, 2023
Primary completion
Dec 2026 (estimated)
Results posted
No
Registry record
NCT05948475 · updated Jul 6, 2026