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OncoMatch/Clinical Trials/NCT06930755

Study of NMS-03305293 in Adult Patients With Relapsed Ovarian Cancer

Is NCT06930755 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies multiple treatments including NMS-03305293 and Topotecan for ovarian cancer.

Phase 1RecruitingNerviano Medical SciencesNCT06930755Data as of Jun 2026

Treatment: NMS-03305293 · TopotecanThis is a multicenter, open-label Phase Ia/b study on the safety and efficacy of the combination of NMS-03305293 and topotecan in patients with recurrent ovarian cancer, with dose-limiting toxicity (DLT) escalation. The aim of this study is to determine the safety and tolerability, as well as to evaluate the anti-tumor efficacy and pharmacokinetics of NMS-03305293 in combination with topotecan.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

Topotecan

Other

NMS-03305293

Cancer type

Ovarian Cancer

Biomarker criteria

Excluded: BRCA1 mutation

Excluded: BRCA2 mutation

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Female only

Prior therapy

Max 5 prior lines

Must have received: evidence based local standards of care

failed all evidence based local standards of care as per Investigator judgment

Cannot have received: PARP inhibitor

Exception: outside of approved indication and schedules

Prior therapy with PARP inhibitor, outside of approved indication and schedules

Cannot have received: topoisomerase inhibitor

Prior therapy with topoisomerase inhibitors including payloads of Antibody-Drug Conjugates (ADCs)

Cannot have received: wide-field radiotherapy

Exception: affecting at least 20 percent of the bone marrow

Patients with prior wide-field radiotherapy (RT) affecting at least 20 percent of the bone marrow

Cannot have received: anti-tumor treatment

Exception: within 2 weeks prior to treatment start or 5 half-lives, whichever is longer

Prior anti-tumor treatment within 2 weeks prior to treatment start or 5 half-lives, whichever is longer

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

US trial sites

  • OSF Saint Francis Medical Center · Peoria, Illinois
  • Washington University School of Medicine in St. Louis · St Louis, Missouri
  • Penn Medicine - Perelman Center for Advanced Medicine · Philadelphia, Pennsylvania
  • Tennessee Oncology · Nashville, Tennessee
  • The University of Texas MD Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06930755 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior PARP inhibitor, topoisomerase inhibitor, wide-field radiotherapy disqualifies patients from enrollment.

Are patients with BRCA1 alterations eligible?

No. BRCA1 mutation is an exclusion criterion.

Are patients with BRCA2 alterations eligible?

No. BRCA2 mutation is an exclusion criterion.

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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