Clinical trial · Interventional
A Study of TAS-120 in Patients With Metastatic Breast Cancer
A Phase 2 Study of TAS-120 in Metastatic Breast Cancers Harboring Fibroblast Growth Factor Receptor (FGFR) Amplifications
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): The Sponsor decided to discontinue the study due to strategic considerations and not due to any safety-related concerns.
Summary
Brief summary (as posted)
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.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| FGFR 1 High Amplification | — | UNRESOLVED | — |
| FGFR2 Amplification | — | UNRESOLVED | — |
| Metastatic Breast Cancer | Malignant Breast Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Futibatinib | Drug | Futibatinib | ALIAS |
| Futibatinib plus Fulvestrant | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- Futibatinib (Cohort 1)
- description
- Participants with advanced or metastatic hormone receptor - positive (HR+), human epidermal growth factor receptor 2 - negative (HER2-) breast cancer, harboring fibroblast growth factor receptor 2 (FGFR2) gene amplification, with measurable disease received futibatinib, 20 milligrams (mg), oral tablets, once daily for a continuous 28-day cycle up to maximum of 244 days.
- interventionNames
- Drug: Futibatinib
- type
- EXPERIMENTAL
- label
- Futibatinib (Cohort 2)
- description
- Participants with advanced or metastatic triple negative breast cancer (TNBC), harboring FGFR2 gene amplification, with measurable disease received futibatinib, 20 mg, oral tablets, once daily for a continuous 28-day cycle up to maximum of 1066 days.
- interventionNames
- Drug: Futibatinib
- type
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Provide written informed consent 2. Age ≥ 18 years of age 3. Histologically or cytologically confirmed recurrent locally advanced or metastatic breast cancer not amenable to treatment with curative intent, and the following cohort specific criteria: A. Cohort 1 * HR+ HER2- breast cancer harboring an FGFR2 gene amplification. * Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 * Has received 1-3 prior endocrine-containing therapies and up to 2 prior chemotherapy regimens for advanced/metastatic disease * Has received prior treatment with a CDK4/6 inhibitor or is ineligible for such treatment B. Cohort 2 * TNBC harboring an FGFR2 gene amplification * Measurable disease per RECIST 1.1 * Has received at least 1 prior chemotherapy or chemotherapy/immunotherapy (PD-L1/PD-1 inhibitors) regimen for advanced/metastatic disease C. Cohort 3 * TNBC or HR+ HER2- breast cancer harboring an FGFR2 gene amplification * Non measurable, evaluable disease per RECIST 1.1. Patients with bone-only disease must have lytic or mixed lytic-blastic lesions * Other criteria for either HR+ HER2- breast cancer or TNBC should be met as described for Cohort 1 and 2, respectively D. Cohort 4 * HR+ HER2- breast cancer harboring an FGFR1 high-level gene amplification * Measurable disease per RECIST 1.1 * Has received 1-2 prior endocrine-containing therapies and no more than 1 prior chemotherapy regimen for advanced/metastatic disease. Prior treatment with fulvestrant is not permitted. * Has received prior treatment with a CDK4/6 inhibitor or is ineligible for such treatment * Pre/peri-menopausal patients must be on goserelin 4. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 5. Archival or (preferably) fresh tumor tissue must be available 6. Adequate organ function Exclusion Criteria: 1. History and/or current evidence of any of the following disorders: 1. Non-tumor related alteration of the calcium-phosphorus homeostasis that is considered clinically significant 2. Ectopic mineralization/calcification, including but not limited to soft tissue, kidneys, intestine, or myocardia and lung, considered clinically significant 3. Retinal or corneal disorder confirmed by retinal/corneal examination and considered clinically significant 2. Prior treatment with an FGFR inhibitor 3. A serious illness or medical condition(s) 4. Brain metastases that are untreated or clinically or radiologically unstable 5. Pregnant or lactating female
References
Publications (0)
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