Expanded Access Study of TAS-120 in Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements

NCT04507503 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2026-03-10

No results posted yet for this study

Summary

The objective of the study is to provide access to TAS-120 to patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements.

Conditions

  • Advanced Cholangiocarcinoma

Interventions

DRUG

TAS-120

Futibatinib 20mg QD orally on a 28 days cycle

Sponsors & Collaborators

  • Taiho Oncology, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04507503 on ClinicalTrials.gov