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OncoMatch/Clinical Trials/NCT07069335

A Bioequivalence Study to Evaluate Pharmacokinetics and Safety of BR2022 and BR2022-1 in Patients With Deleterious or Suspected Deleterious Germline BRCA-Mutated Advanced Ovarian Cancer

Is NCT07069335 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Olaparib 150 MG for ovarian cancer.

Phase 1RecruitingBoryung Pharmaceutical Co., LtdNCT07069335Data as of May 2026

Treatment: Olaparib 150 MGThis was a multicenter, open-label, randomized, crossover bioequivalence study to evaluate the pharmacokinetics and safety of BR2022 and BR2022-1 in Patients with deleterious or suspected deleterious germline BRCA-mutated advanced ovarian cancer.

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Extracted eligibility criteria

Cancer type

Ovarian Cancer

Biomarker criteria

Required: BRCA1 deleterious or suspected deleterious germline or somatic mutation

deleterious or suspected deleterious germline or somatic BRCA-mutated

Required: BRCA2 deleterious or suspected deleterious germline or somatic mutation

deleterious or suspected deleterious germline or somatic BRCA-mutated

Disease stage

Metastatic disease required

advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer

Prior therapy

Must have received: PARP inhibitor (olaparib)

have been taking stable doses of olaparib for more than 3 months before screening

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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