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A First-in-Human Study of MEN2501 in Participants With Platinum-Resistant Ovarian Cancer

A First-in-Human Study of MEN2501 in Participants With Platinum-Resistant Ovarian Cancer

Recruiting
18 years and older
Female
Phase 1
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Overview

This is a first-in-human, open-label, dose-escalation, dose-optimization trial designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and antitumor activity of MEN2501 monotherapy in adult participants with platinum-resistant ovarian cancer.

Eligibility

Key Inclusion Criteria:

  • Participants must have a histopathologically confirmed diagnosis of high-grade serous ovarian cancer, primary peritoneal cancer, or fallopian tube cancer.

Key Exclusion Criteria:

  • Participants with primary platinum-refractory disease.

Note: Other protocol-defined inclusion/exclusion criteria may apply.

Study details
    Platinum-resistant Ovarian Cancer

NCT07226427

Stemline Therapeutics, Inc.

31 January 2026

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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