RecruitingPhase 1NCT06930755

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

Study of NMS-03305293, a Non-Trapping PARP1-Specific PARP Inhibitor in Relapsed Ovarian Cancer


Sponsor

Nerviano Medical Sciences

Enrollment

24 participants

Start Date

May 13, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This 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.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a new investigational drug called NMS-03305293 for women with relapsed high-grade serous ovarian, fallopian tube, or peritoneal cancer who have not responded well to prior treatments. **You may be eligible if...** - You are an adult woman with high-grade serous ovarian, fallopian tube, or peritoneal cancer confirmed by a tissue sample - Your cancer has progressed after your most recent line of treatment - You have received no more than 5 prior treatment regimens - You have at least one measurable tumor - You are in good enough health (ECOG performance status of 2 or lower) **You may NOT be eligible if...** - You are currently enrolled in another clinical trial - You have a BRCA gene mutation or specific genetic features associated with DNA repair problems - You have been previously treated with PARP inhibitors (a type of targeted therapy) - You are currently receiving other cancer treatments Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGNMS-03305293

Route of administration: Oral

DRUGTopotecan

Route of administration: Intravenous


Locations(5)

OSF Saint Francis Medical Center

Peoria, Illinois, United States

Washington University School of Medicine in St. Louis

St Louis, Missouri, United States

Penn Medicine - Perelman Center for Advanced Medicine

Philadelphia, Pennsylvania, United States

Tennessee Oncology

Nashville, Tennessee, United States

The University of Texas MD Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06930755


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