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

Abroad (travel likely)RecruitingPHASE2

Conditions

Multiple Myeloma

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
  • 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
Study leads
  • Bristol-Myers Squibb

    Study Director

    Bristol-Myers Squibb