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Clinical Trial Summary

A phase II, open-label, multicenter study to evaluate the efficacy and safety of oral TT-00420 (Tinengotinib) tablets in subjects with cholangiocarcinoma who failed or relapsed to prior treatment of chemotherapy and FGFR Inhibitor.


Clinical Trial Description

Approximately 50 subjects will be enrolled. Eligible subjects will receive tinengotinib 10 mg QD orally as the initial dose level in 21-day cycles until confirmed disease progression, intolerable toxicity, death, or withdrawal of consent. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06057571
Study type Interventional
Source TransThera Sciences (Nanjing), Inc.
Contact Caixia Sun, PhD
Phone 025-58216298
Email sun_caixia@transtherabio.com
Status Recruiting
Phase Phase 2
Start date November 17, 2023
Completion date October 31, 2025

See also
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Recruiting NCT05053555 - High Dose-Rate Brachytherapy for the Treatment of Both Primary and Secondary Unresectable Liver Malignancies N/A