Clin2
NCT07504588Possibly a fitRecruiting

Comparing two drug combinations for recurrent ovarian cancer after PARP inhibitor treatment

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 tests whether a new drug combination (sacituzumab govitecan plus bevacizumab) works better than the usual chemotherapy for ovarian cancer that has come back after platinum treatment and PARP inhibitor maintenance. It may offer a new option for people with certain genetic markers (BRCA mutations or HRD).

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 a type of ovarian cancer that is high-grade serous or endometrioid (including fallopian tube or primary peritoneal cancer).
  • Your cancer is platinum-sensitive, meaning it responded to platinum chemo and then came back at least 6 months after your last platinum dose.
  • You have already taken a PARP inhibitor (like olaparib, niraparib, or rucaparib) as maintenance after first-line treatment, and your cancer has progressed on that. You cannot have had any other treatment in between.
  • You have a BRCA1 or BRCA2 mutation (inherited or in the tumor) or a test showing homologous recombination deficiency (HRD).
  • You have not had topoisomerase-I inhibitors (a type of chemo) before, and you have recovered from side effects of prior treatments.
  • You are at least 18 years old, not pregnant, and have adequate organ function (kidney, liver, blood counts).

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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