Dose-escalation and Dose-expansion Study of Safety of Azer-cel (PBCAR0191) in Participants With Relapsed/Refractory (r/r) Non-Hodgkin Lymphoma (NHL) and r/r B-cell Acute Lymphoblastic Leukemia (B-ALL)

חו"ל (דורש נסיעה)מגייס משתתפיםPHASE1

מצבים רפואיים

Non-Hodgkin Lymphoma · B-cell Acute Lymphoblastic Leukemia · Chronic Lymphocytic Leukemia · Small Lymphocytic Lymphoma

סיכום בשפה פשוטהבעזרת בינה מלאכותית

הסיכום נכתב על־ידי מודל שפה והוא ניסיוני. המידע עלול להיות חלקי או שגוי ואינו תחליף לייעוץ רפואי.

מיקומים
  • Banner MD Anderson Cancer Center, Gilbert, Arizona, United States

  • City of Hope, Duarte, California, United States

  • H. Lee Moffitt Cancer Center, Tampa, Florida, United States

    Contact: Study coordinator (Clinical Research)
    Contact: Principal Investigator (Bijal Shah, MD)
  • Winship Cancer Institute Emory University, Atlanta, Georgia, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Edmund Waller, MD)
  • Northside Hospital Cancer Institute, Atlanta, Georgia, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Scott Solomon, MD)
  • University of Maryland, Baltimore, Maryland, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Jean Yared, MD)
  • Tufts Medical Center, Boston, Massachusetts, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Andreas Klein, MD)
  • Dana-Farber Cancer Institute, Boston, Massachusetts, United States

  • Barbara Ann Karmanos Cancer Institute (Wayne State University), Detroit, Michigan, United States

  • University of Minnesota, Minneapolis, Minnesota, United States

    Contact: Study coordinator (Clinical Research)
    Contact: Principal Investigator (Supriya Gupta, MD)
  • Weill Cornell Medical College - NY Presbyterian Hospital, New York, New York, United States

  • Columbia University Irving Medical Center/New York Presbyterian Hospital, New York, New York, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Ran Reshef, MD)
  • Duke University, Durham, North Carolina, United States

  • Ohio State University, Columbus, Ohio, United States

  • Lifespan Cancer Institute at Rhode Island Hospital, Providence, Rhode Island, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Adam Olszewski, MD)
  • Baylor University Medical Center, Dallas, Texas, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Houston Holmes III, MD)
  • MD Anderson, Houston, Texas, United States

  • Medical College of Wisconsin, Milwaukee, Wisconsin, United States

    Contact: Study coordinator (Clinical Trials)
    Contact: Principal Investigator (Nirav Shah, MD)
  • Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia

    Contact: Study coordinator (Dr Vinay Vanguru)
  • Liverpool Hospital, Liverpool, New South Wales, Australia

    Contact: Study coordinator (Dr Nagendra P Sungala)
  • Royal Adelaide Hospital, Adelaide, South Australia, Australia

    Contact: Study coordinator (Dr Danielle Blunt)
  • St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia

    Contact: Principal Investigator (Matthew Ku)
  • Barwon Health - Andrew Love Cancer Centre, Geelong, Victoria, Australia

    Contact: Principal Investigator (Hannah Rose)
מובילי המחקר
  • John Byon, MD, PhD

    Study Chair

    Imugene Limited