Clin2
NCT07504588Possibly a fitNot yet recruiting

Comparing two treatments for recurrent ovarian cancer after PARP inhibitor therapy

Recurrent Platinum-Sensitive Fallopian Tube Endometrioid AdenocarcinomaRecurrent Platinum-Sensitive Fallopian Tube High Grade Serous AdenocarcinomaRecurrent Platinum-Sensitive Ovarian High Grade Endometrioid AdenocarcinomaRecurrent Platinum-Sensitive Ovarian High Grade Serous AdenocarcinomaRecurrent Platinum-Sensitive Primary Peritoneal Endometrioid AdenocarcinomaRecurrent Platinum-Sensitive Primary Peritoneal High Grade Serous Adenocarcinoma

Treatments studied

Part of Cancer, Women’s health & pregnancy clinical trials.

This trial compares a combination of two drugs (sacituzumab govitecan and bevacizumab) to standard chemotherapy for ovarian cancer that has come back after treatment with a PARP inhibitor. It is for people whose cancer has a BRCA mutation or is homologous recombination deficient.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
87 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have been diagnosed with high-grade serous or endometrioid ovarian cancer, which includes fallopian tube or primary peritoneal cancer.
  • Your cancer responded to platinum-based chemotherapy for at least 6 months before coming back.
  • Your cancer got worse while you were on your first maintenance PARP inhibitor treatment (like Olaparib or Niraparib).
  • Your tumor has a BRCA1 or BRCA2 mutation (inherited or found in the tumor) or is positive for homologous recombination deficiency (HRD).
  • You have not had any treatment with a topoisomerase-I inhibitor before (like irinotecan or topotecan).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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