Study of Futibatinib in Patients With Advanced Cholangiocarcinoma With FGFR2 Fusion or Rearrangement

Part of paid clinical trials in La Jolla, California.

Sponsor
Taiho Oncology, Inc.
Study ID
NCT05727176
Phase
PHASE2
Status
Recruiting

Conditions

  • Advanced Cholangiocarcinoma
  • FGFR2 Fusions
  • Gene Rearrangement

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • TAS-120 — DRUG
    TAS-120 is an oral FGFR inhibitor

Study Details

This is an open-label, multinational, randomized Phase 2 study confirming the clinical benefit of 20 mg futibatinib and evaluating the safety and efficacy of 16 mg futibatinib in previously treated CCA harboring FGFR2 gene fusions and other rearrangements.

Key Dates

First listed
Feb 14, 2023
Start date
Jul 5, 2023
Status verified
Jul 2026
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
120 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Treatment Arm A
    TAS-120 (20mg) tablets, oral; 21-day cycle
  • Experimental: Treatment Arm B
    TAS-120 (16mg) tablets, oral; 21-day cycle

Primary Outcome Measure

ORR by independent central review [ Time Frame: 12 months after the study completion ]

Central Contacts

Locations (10)

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