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OncoMatch/Clinical Trials/NCT06855069

HS-20089 for Injection in Patients With Platinum-Resistant Recurrent Epithelial Ovarian Cancer

Is NCT06855069 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies multiple treatments including HS-20089 and Paclitaxel for ovarian cancer.

Phase 3RecruitingHansoh BioMedical R&D CompanyNCT06855069Data as of Jun 2026Location: China

Treatment: HS-20089 · Paclitaxel · Doxorubicin · TopotecanThis study is a randomized, open-label, controlled, phase III study to evaluate the efficacy and safety of HS-20089 versus investigator's choice of chemotherapy in patients with platinum-resistant recurrent epithelial ovarian cancer.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

PaclitaxelDoxorubicinTopotecan

Other

HS-20089

Cancer type

Ovarian Cancer

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Female only

Prior therapy

Must have received: platinum-based chemotherapy

Patients must have platinum-resistant disease

Cannot have received: TOP1 inhibitor

Prior treated with TOP1 inhibitors

Cannot have received: antibody-drug conjugate

Exception: if payload is TOP1 inhibitor

ADCs with TOP1 inhibitors as payload

Lab requirements

Blood counts

adequate bone marrow reserve

Kidney function

adequate organ function

Liver function

adequate organ function

Adequate bone marrow reserve and organ function.

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

Frequently asked questions

Is NCT06855069 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior TOP1 inhibitor, antibody-drug conjugate disqualifies patients from enrollment.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

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

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