Study of Arlocabtagene Autoleucel (BMS-986393) a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma

חו"ל (דורש נסיעה)מגייס משתתפיםPHASE2

מצבים רפואיים

Multiple Myeloma

סיכום בשפה פשוטהבעזרת בינה מלאכותית

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

מיקומים
  • University of Alabama at Birmingham, Birmingham, Alabama, United States

    Contact: Study coordinator (Susan Bal) · 205-934-1908
  • Banner MD Anderson Cancer Center, Gilbert, Arizona, United States

    Contact: Study coordinator (Ambuga Badari)
  • University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States

    Contact: Study coordinator (Sharmilan Thanendrarajan) · 000-000-0000
  • UCLA Hematology/Oncology - Westwood (Building 200 Suite 214), Los Angeles, California, United States

    Contact: Study coordinator (Sarah Larson) · 310-829-5471
  • UCSF Helen Diller Medical Center at Parnassus Heights, San Francisco, California, United States

    Contact: Study coordinator (Anupama Kumar) · 415-514-0768
  • Colorado Blood Cancer Institute, Denver, Colorado, United States

    Contact: Study coordinator (Tara Gregory) · 720-754-4800
  • Mayo Clinic in Florida, Jacksonville, Florida, United States

    Contact: Study coordinator (Vivek Roy) · 000-000-0000
  • Miami Cancer Institute at Baptist Health, Inc., Miami, Florida, United States

    Contact: Study coordinator (George Nahas) · 201-310-8558
  • Moffitt Cancer Center, Tampa, Florida, United States

    Contact: Study coordinator (Ciara Freeman) · 813-745-2475
  • Winship Cancer Institute of Emory University, Atlanta, Georgia, United States

    Contact: Study coordinator (Nisha Joseph) · 502-608-5503
  • Northside Hospital, Atlanta, Georgia, United States

    Contact: Study coordinator (Scott Solomon) · 404-255-1930
  • Northwestern Memorial Hospital, Chicago, Illinois, United States

    Contact: Study coordinator (Seema Singhal) · 312-505-1290
  • University of Chicago Medical Center, Chicago, Illinois, United States

    Contact: Study coordinator (Jennifer Cooperrider)
  • University of Iowa, Iowa City, Iowa, United States

    Contact: Study coordinator (Christopher Strouse) · 630-917-8956
  • The University of Kansas Cancer Center - Westwood, Westwood, Kansas, United States

    Contact: Study coordinator (Leyla Shune) · 913-588-6029
  • Norton Women's and Children's Hospital, Louisville, Kentucky, United States

    Contact: Study coordinator (Don Stevens) · 502-899-3366
  • Local Institution - 0065, Baltimore, Maryland, United States

  • Massachusetts General Hospital, Boston, Massachusetts, United States

    Contact: Study coordinator (Diana Cirstea) · 617-724-4000
  • Dana-Farber Cancer Institute, Boston, Massachusetts, United States

    Contact: Study coordinator (Omar Nadeem) · 617-632-3000
  • Mayo Clinic in Rochester, Minnesota, Rochester, Minnesota, United States

    Contact: Study coordinator (Taxiarchis Kourelis) · 855-776-0015
  • Washington University School of Medicine, St Louis, Missouri, United States

    Contact: Study coordinator (Michael Slade) · 314-454-8304
  • Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, United States

    Contact: Study coordinator (Mansi Shah) · 732-209-5479
  • Roswell Park Cancer Institute, Buffalo, New York, United States

    Contact: Study coordinator (Ehsan Malek) · 216-286-4441
  • Icahn School of Medicine at Mount Sinai, New York, New York, United States

    Contact: Study coordinator (Adriana Rossi) · 646-962-6500
  • Memorial Sloan Kettering Cancer Center, New York, New York, United States

    Contact: Study coordinator (Sham Mailankody) · 646-608-3712
  • University of North Carolina Medical Center, Chapel Hill, North Carolina, United States

    Contact: Study coordinator (Eben Lichtman) · 617-842-6051
  • Local Institution - 0067, Charlotte, North Carolina, United States

  • Oncology Hematology Care, Cincinnati, Ohio, United States

    Contact: Study coordinator (Kruti Patel) · 888-961-4156
  • The James Cancer Hospital and Solove Research Institute at The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States

    Contact: Study coordinator (Srinivas Devarakonda) · 570-423-0522
  • Oregon Health and Science University, Portland, Oregon, United States

    Contact: Study coordinator (Amrita Desai) · 503-494-0896
  • Sidney Kimmel Cancer Center - Jefferson Health, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (Usama Gergis) · 917-698-4310
  • Tennessee Oncology, Nashville, Tennessee, United States

    Contact: Study coordinator (Jesus Berdeja) · 615-329-0570
  • Vanderbilt University Medical Center, Nashville, Tennessee, United States

    Contact: Study coordinator (Muhamed Baljevic) · 917-913-9166
  • Local Institution - 0069, Austin, Texas, United States

  • UT Southwestern Medical Center, Dallas, Texas, United States

    Contact: Study coordinator (Larry Anderson) · 214-648-5906
  • University of Texas MD Anderson Cancer Center, Houston, Texas, United States

    Contact: Study coordinator (Krina Patel) · 713-792-6662
  • Methodist HealthCare System of San Antonio Clinical Trials Office, Texas Transplant Institute, San Antonio, Texas, United States

    Contact: Study coordinator (Paul Shaughnessy) · 210-670-2313
  • LDS Hospital, Salt Lake City, Utah, United States

    Contact: Study coordinator (Bradley Hunter) · 801-408-3729
  • Virginia Oncology Associates, Norfolk, Virginia, United States

    Contact: Study coordinator (gary Simmons) · 757-461-7084
  • Fred Hutchinson Cancer Center, Seattle, Washington, United States

    Contact: Study coordinator (Rahul Banerjee) · 206-606-1453
  • University of Wisconsin Carbone Cancer Center - University Hospital, Madison, Wisconsin, United States

    Contact: Study coordinator (Zhubin Gahvari) · 608-262-9317
  • Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia

    Contact: Study coordinator (Joy Ho) · +61295158031
  • Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia

    Contact: Study coordinator (Nicholas Weber) · +61736460818
  • The Alfred Hospital, Melbourne, Victoria, Australia

    Contact: Study coordinator (Sueh-Li Lim) · 0403374221
  • St Vincent's Hospital, Melbourne, Victoria, Australia

    Contact: Study coordinator (Hang Quach) · 61392882698
  • Arthur J.E. Child Comprehensive Cancer Centre, Calgary, Alberta, Canada

    Contact: Study coordinator (Nizar Bahlis) · 4032202801
  • McGill University Health Centre, Montreal, Quebec, Canada

    Contact: Study coordinator (Michael Sebag) · 514-934-1934-31558
  • Nagoya City University Hospital, Nagoya, Aichi-ken, Japan

    Contact: Study coordinator (Shinsuke Iida) · 81528515511
  • Hyogo Medical University Hospital, Nishinomiya, Hyōgo, Japan

    Contact: Study coordinator (Satoshi Yoshihara) · +81-90-2102-4734
  • Chiba University Hospital, Chiba, Japan

    Contact: Study coordinator (Emiko Sakaida) · +81432227171
  • University Hospital,Kyoto Prefectural University of Medicine, Kyoto, Japan

    Contact: Study coordinator (Junya Kuroda) · 81752515740
  • Japanese Red Cross Medical Center, Tokyo, Japan

    Contact: Study coordinator (Tadao Ishida) · 8133400104
מובילי המחקר
  • Bristol-Myers Squibb

    Study Director

    Bristol-Myers Squibb