Capmatinib rollover study offers continued treatment for cMET-Dependent cancer patients

NCT ID NCT03040973

First seen Nov 01, 2025 · Last updated May 25, 2026 · Updated 23 times

Summary

This study gives patients with advanced cMET-dependent solid tumors continued access to capmatinib, a targeted cancer drug, after completing a previous Novartis-sponsored trial. The main goal is to monitor long-term safety and side effects. About 29 participants who are already benefiting from capmatinib alone or in combination will be followed closely.

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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

  • Massachusetts General Hospital

    Boston, Massachusetts, 02114, United States

  • Novartis Investigative Site

    Leuven, 3000, Belgium

  • Novartis Investigative Site

    Edmonton, Alberta, T6G 1Z2, Canada

  • Novartis Investigative Site

    Shanghai, Shanghai Municipality, 200433, China

  • Novartis Investigative Site

    Kunming, Yunnan, 650106, China

  • Novartis Investigative Site

    Copenhagen, DK-2100, Denmark

  • Novartis Investigative Site

    Dijon, Cote D Or, 21034, France

  • Novartis Investigative Site

    Cologne, North Rhine-Westphalia, 50937, Germany

  • Novartis Investigative Site

    Hanover, 30625, Germany

  • Novartis Investigative Site

    Perugia, PG, 06129, Italy

  • Novartis Investigative Site

    Milan, 20141, Italy

  • Novartis Investigative Site

    Singapore, 119074, Singapore

  • Novartis Investigative Site

    Seoul, 03080, South Korea

  • Novartis Investigative Site

    Seoul, 05505, South Korea

  • Novartis Investigative Site

    Madrid, 28040, Spain

Conditions

Explore the condition pages connected to this study.