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Completed Phase 1Phase 2 Interventional Results available

A Study of TAS-120 in Patients With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT02052778

Public ClinicalTrials.gov record NCT02052778. 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 Oct 21, 2026, 12:49 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

Phase 1/2 Study of TAS-120 in Patients With Advanced Solid Tumors Harboring FGF/FGFR Aberrations

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an open-label, nonrandomized, Phase 1/2 study for the fibroblast growth factor receptor (FGFR) inhibitor futibatinib (TAS-120). The purpose of the study is to evaluate the safety, tolerability, pharmacokinetic, pharmacodynamic, and anti-tumor activity of futibatinib in patients with advanced solid tumors with and without genomic FGF/FGFR abnormalities. The study will be conducted in 3 parts: 1. Dose escalation portion to determine the -Maximum Tolerated Dose and/ or Recommended Phase 2 Dose of futibatinib. 2. Phase 1 expansion portion to further evaluate the safety and efficacy of futibatinib in patients with tumors harboring FGF/FGFR aberrations, including patients with cholangiocarcinoma (CCA), primary central nervous system tumors, urothelial carcinoma, breast cancer, gastric cancer. 3. Phase 2 study portion to confirm objective response rate of futibatinib in intrahepatic CCA patients with tumors harboring FGFR2 gene rearrangements (incl fusions).

Study identification

NCT ID
NCT02052778
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Taiho Oncology, Inc.
Industry
Enrollment
407 participants

Conditions and interventions

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
Jul 21, 2014 (Actual)
Primary completion
Oct 1, 2020 (Actual)
Completion
Oct 22, 2024 (Actual)
Last update posted
Mar 27, 2025

2014 – 2024

United States locations

U.S. sites
26
U.S. states
17
U.S. cities
24
Facility City State ZIP Site status
Banner MD Anderson Cancer Center Gilbert Arizona 85234 —
Mayo Clinic (AZ) Scottsdale Arizona 85259 —
The University of Arizona Cancer Center - North Campus Tucson Arizona 85719 —
City of Hope National Medical Center Duarte California 91010 —
UCSF Helen Diller Family Comprehensive Cancer Center. Mission Bay San Francisco California 94158 —
Cancer Treatment Centers of America Newnan Georgia 30265 —
Cancer Treatment Centers of America Zion, IL Zion Illinois 60099 —
The University of Kansas Cancer Center Fairway Kansas 66205 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Dana Farber Cancer Institution Boston Massachusetts 02215 —
Wayne State Universtity (Karmanos Cancer Institute) Detroit Michigan 48201 —
Mayo Clinic (MN) Rochester Minnesota 55905 —
New Mexico Cancer Care Alliancer Albuquerque New Mexico 87106 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104 —
Sidney Kimmel Cancer Center at Jefferson Philadelphia Pennsylvania 19107 —
University of Pittsburgh Medical Center Hillman Cancer Center Pittsburgh Pennsylvania 15232 —
Greenville Health System ITOR,Clinical Research Unit Greenville South Carolina 29605 —
Spartanburg Medical Center Spartanburg South Carolina 29303 —
Mary Crowley Cancer Research - Medical City Dallas Texas 75230 —
The University of Texas MD Anderson Cancer Center Houston Texas 77030 —
University of Utah, Huntsman Cancer Hospital Salt Lake City Utah 84112 —
University of Virginia Cancer Center Charlottesville Virginia 22903 —
Virginia Mason Cancer Center Seattle Washington 98101 —
University of Wisconsin Clinical Science Center Madison Wisconsin 53792 —
Medical College of Wisconsin Milwaukee Wisconsin 53226 —

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 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02052778, 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 Mar 27, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02052778 live on ClinicalTrials.gov.

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