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New pill shows promise for tough ovarian cancer

NCT ID NCT06084416

First seen Nov 01, 2025 · Last updated May 22, 2026 · Updated 30 times

Summary

This study tests a new oral drug called sovilnesib in people with advanced high-grade serous ovarian cancer that no longer responds to platinum chemotherapy. The main goal is to find the best dose that is safe and effective. About 120 adults will take the pill daily, and researchers will monitor side effects and tumor response.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Corewell Health

    Grand Rapids, Michigan, 49503, United States

  • Dana Farber Cancer Institute

    Boston, Massachusetts, 02215, United States

  • Fred Hutchinson Cancer Center

    Seattle, Washington, 98109, United States

  • Georgia Cancer Center Augusta University

    Atlanta, Georgia, 30912, United States

  • Hoag Memorial Hospital

    Newport Beach, California, 92663, United States

  • Icahn School of Medicine at Mount Sinai

    New York, New York, 10128, United States

  • Johns Hopkins Hospital

    Baltimore, Maryland, 21287, United States

  • MUSC Hollings Cancer Center

    Charleston, South Carolina, 29020, United States

  • OU Health Stephenson Cancer Center

    Oklahoma City, Oklahoma, 73117, United States

  • Roswell Park Comprehensive Cancer Center

    Buffalo, New York, 14263, United States

  • The University of Alabama at Birmingham

    Birmingham, Alabama, 35294, United States

  • UCLA

    Los Angeles, California, 90095, United States

  • University of Arkansas for Medical Sciences

    Little Rock, Arkansas, 72205, United States

Conditions

Explore the condition pages connected to this study.