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Active, not recruiting Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT05948475

Public ClinicalTrials.gov record NCT05948475. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 7:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Study identification

NCT ID
NCT05948475
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
TransThera Sciences (Nanjing), Inc.
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

  • Tinengotinib 8 mg Drug
  • Tinengotinib 10 mg Drug
  • Physician's Choice Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 19, 2023
Primary completion
Nov 30, 2026
Completion
Nov 30, 2026
Last update posted
Jul 5, 2026

2023 – 2026

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
UCLA Medical Center Santa Monica California 90401
Stanford Cancer Center Stanford California 94305
The University of Kansas Cancer Center Westwood, Los Angeles California 90024
Mount Sinai Comprehensive Cancer Center Miami Beach Florida 33140
The University of Chicago Hospitals Chicago Illinois 60601
UMass Memorial Medical Center Worcester Massachusetts 01655
University of Michigan Ann Arbor Michigan 48103
Henry Ford Detroit Michigan 48201
University of Minnesota- Masonic Cancer Center, M Health Fairview Minneapolis Minnesota 55455
Roswell Park Comprehensive Cancer Center Buffalo New York 14263
Messino Cancer Centers Asheville North Carolina 28806
University Hospitals Cleveland Medical Center Cleveland Ohio 44106
Tennessee Oncology- Nashville Nashville Tennessee 37203
Vanderbilt-Ingram Cancer Center Nashville Tennessee 37203
University of Texas Southwestern Medical Center Dallas Texas 75201
Texas Oncology-Sammons Cancer Center Dallas Texas 75246
The University of Texas MD Anderson Cancer Center Houston Texas 77002
University of Virginia Cancer Center Charlottesville Virginia 22908
Medical College of Wisconsin Milwaukee Wisconsin 53202

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 68 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05948475, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 5, 2026 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05948475 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →