BRCA Mutation clinical trials at UCSF

1 research study open to eligible people

BRCA mutations are genetic changes linked to higher cancer risk. UCSF is studying how Olaparib and ASTX727 work together in treating tumors with these mutations. This research aims to improve treatment options for people with BRCA1/2 and other similar genetic changes.

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  • Olaparib and ASTX727 in BRCA1/2- and Homologous Recombination Deficient (HRD)-Mutated Tumors

    open to eligible people ages 18 years and up

    This is a single center, phase I/Ib clinical trial evaluating the combination of the poly adenosine diphosphate-ribose polymerase (PARP) inhibitor olaparib with the DNA methyltransferase (DNMT) inhibitor ASTX727, which is an oral formulation of decitabine with cedazuridine (a cytidine deaminase inhibitor that allows for oral administration). The study population consists of adults with advanced/metastatic solid tumor malignancies with germline or somatic mutations in the HRR pathway (i.e., BReast CAncer gene 1 (BRCA1), BReast CAncer gene 2(BRCA2), Partner And Localizer of BRCA2 (PALB2), ATM, and/or Checkpoint kinase 2 (CHEK2) mutations).

    San Francisco, California

Our lead scientists for BRCA Mutation research studies include .

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