Study to Determine the Efficacy and Safety of Asciminib in Pediatric Patients With Ph+ CML-CP

Abroad (travel likely)RecruitingPHASE2

Conditions

Chronic Myelogenous Leukemia · Leukemia, Myelogenous, Chronic, Philadelphia Chromosome Positive

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations
  • Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, United States

    Contact: Study coordinator (Jesmin Habeeb Mohamed) · jsh216@cinj.rutgers.edu
    Contact: Principal Investigator (Richard DRACHTMAN)
  • Columbia University Medical Center New York Presbyterian, New York, New York, United States

    Contact: Study coordinator (Karishma Sookraj) · kss2158@cumc.columbia.edu · 212-305-6953
    Contact: Principal Investigator (Nobuko Hijiya)
  • Novartis Investigative Site, Brisbane, Queensland, Australia

  • Novartis Investigative Site, North Adelaide, South Australia, Australia

  • Novartis Investigative Site, Montreal, Quebec, Canada

  • Novartis Investigative Site, Zhengzhou, Henan, China

  • Novartis Investigative Site, Tianjin, China

  • Novartis Investigative Site, Marseille, France

  • Novartis Investigative Site, Paris, France

  • Novartis Investigative Site, Strasbourg, France

  • Novartis Investigative Site, Yokohama, Kanagawa, Japan

  • Novartis Investigative Site, Saitama, Japan

  • Novartis Investigative Site, Utrecht, Netherlands

  • Novartis Investigative Site, Seoul, South Korea

  • Novartis Investigative Site, Seoul, South Korea

  • Novartis Investigative Site, Madrid, Spain

Study leads
  • Novartis Pharmaceuticals

    Study Director

    Novartis Pharmaceuticals