drugset / Trial / NCT07060365

A Master Protocol Study to Investigate Biomarker-guided Novel Anticancer Agent(s) as Monotherapy or Combination Therapy in Participants With Advanced/Recurrent Ovarian Cancer

NCT07060365

Phase 1/2 Withdrawn AstraZeneca Parexel · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The main purpose of this study is to investigate the safety, tolerability, preliminary efficacy, pharmacokinetics (PK) and pharmacodynamics (PD) of biomarker-guided novel anticancer agent(s) as monotherapy or combination therapy for the treatment of participants with advanced/recurrent ovarian cancer. Substudy 1 will investigate the safety, tolerability, preliminary efficacy, PK and PD of saruparib monotherapy in participants with BReast CAncer gene (BRCA) mutated epithelial ovarian, fallopian tube, or primary peritoneal cancer.

Timeline

Start
2025-09-02
Primary completion
2025-12-19
Completion
2025-12-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Saruparib Small molecule Oral

Indications