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FGFR2 Amplification clinical trials at UCSF

2 in progress, 1 open to eligible people

FGFR2 amplification is a genetic change found in some cancer cells. UCSF is currently recruiting patients for a clinical trial called "REFOCUS" that is testing a new drug called RLY-4008. This trial is for patients with advanced solid tumors, including intrahepatic cholangiocarcinoma (ICC). There is also another trial in progress, but it is not accepting new participants at this time.

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  • REFOCUS: A First-in-Human Study of Highly Selective FGFR2 Inhibitor, RLY-4008, in Patients With ICC and Other Advanced Solid Tumors

    open to eligible people ages 18 years and up

    This is a Phase 1/2, open-label, FIH study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDy), and antineoplastic activity of RLY-4008, a potent and highly selective FGFR2 inhibitor, in patients with unresectable or metastatic cholangiocarcinoma (CCA) and other solid tumors. The study consists of 3 parts: a dose escalation (Part 1), a dose expansion (Part 2), and an extension (Part 3).

    San Francisco, California and other locations

  • TAS-120 in Patients With Metastatic Breast Cancer

    Sorry, in progress, not accepting new patients

    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.

    San Francisco, California and other locations

Our lead scientists for FGFR2 Amplification research studies include .

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