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Terminated Phase 2 Interventional Results available

A Study of TAS-120 in Patients With Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT04024436

Public ClinicalTrials.gov record NCT04024436. 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 Sep 6, 2026, 12:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Study of TAS-120 in Metastatic Breast Cancers Harboring Fibroblast Growth Factor Receptor (FGFR) Amplifications

Brief summary

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

The purpose of the trial is to evaluate a patient's response to a Fibroblast Growth Factor Receptor (FGFR) inhibitor, futibatinib (TAS-120), used either alone or in combination with the hormonal therapy, fulvestrant. This study will be conducted in patients with metastatic breast cancer who have specific Fibroblast Growth Factor Receptor gene abnormalities and who have previously received conventional therapies to treat their breast cancer, or who are not able to tolerate certain cancer therapies. This study will also evaluate the safety of taking futibatinib, or futibatinib and fulvestrant, by learning about the potential side effects.

Study identification

NCT ID
NCT04024436
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Taiho Oncology, Inc.
Industry
Enrollment
64 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
Jan 27, 2020
Primary completion
May 30, 2023
Completion
Sep 5, 2023
Last update posted
Nov 12, 2025

2020 – 2023

United States locations

U.S. sites
17
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
Mayo Clinic - AZ Phoenix Arizona 85054
USCF San Francisco California 94115
Florida Cancer Specialists Fort Myers Florida 33901
Mayo Clinic - FL Jacksonville Florida 32224
Florida Cancer Specialists St. Petersburg Florida 33705
Florida Cancer Specialists Tallahassee Florida 32308
Moffitt Cancer Center Tampa Florida 33612
Florida Cancer Specialists West Palm Beach Florida 33401
Massachusetts General Hospital Boston Massachusetts 02114
BIDMC Boston Massachusetts 02115
Dana Farber Cancer Institute Boston Massachusetts 02115
Mayo Clinic - MN Rochester Minnesota 55905
HCA Midwest Health Kansas City Missouri 64132
Tennessee Oncology Chattanooga Tennessee 37404
Tennessee Oncology Nashville Tennessee 37203
UT Southwestern Dallas Texas 75390
MD Anderson Houston Texas 77030

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04024436, 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 Nov 12, 2025 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04024436 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →