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A Post-marketing Observational Study of Tasfygo in Participants With Unresectable Biliary Tract Cancer With Fibroblast Growth Factor Receptor 2 (FGFR2) Fusion Gene Positivity Who Progressed After Chemotherapy
RECRUITINGSponsored by Eisai Co., Ltd.
Actively Recruiting
SponsorEisai Co., Ltd.
Started2025-07-10
Est. completion2032-11-20
Eligibility
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06793709
Summary
The primary purpose of this study is to investigate the safety of Tasfygo.
Eligibility
Healthy volunteers accepted
Inclusion Criteria: 1\. Participants with unresectable biliary tract cancer with FGFR2 fusion gene positivity who are naïve to Tasfygo tablet and progressed after chemotherapy. Exclusion Criteria: Not applicable.
Conditions2
Biliary Tract CancerCancer
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Actively Recruiting
SponsorEisai Co., Ltd.
Started2025-07-10
Est. completion2032-11-20
Eligibility
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06793709