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Spots Global Cancer Trial Database for Study of BMS-986393 a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma

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Trial Identification

Brief Title: Study of BMS-986393 a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma

Official Title: A Phase 2, Open-Label, Multicenter Study of BMS-986393, a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma (QUINTESSENTIAL)

Study ID: NCT06297226

Interventions

BMS-986393

Study Description

Brief Summary: The purpose of this study is to evaluate the effectiveness and safety of BMS-986393 in participants with relapsed or refractory multiple myeloma.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Local Institution - 0001, Birmingham, Alabama, United States

Local Institution - 0025, Gilbert, Arizona, United States

Local Institution - 0037, Little Rock, Arkansas, United States

UCLA Hematology/Oncology - Westwood (Building 200 Suite 214), Los Angeles, California, United States

Local Institution - 0018, San Francisco, California, United States

Colorado Blood Cancer Institute, Denver, Colorado, United States

Local Institution - 0045, Miami, Florida, United States

Local Institution - 0029, Tampa, Florida, United States

Local Institution - 0009, Atlanta, Georgia, United States

Local Institution - 0004, Atlanta, Georgia, United States

Local Institution - 0005, Chicago, Illinois, United States

Local Institution - 0056, Chicago, Illinois, United States

University of Iowa, Iowa City, Iowa, United States

Local Institution - 0016, Westwood, Kansas, United States

Local Institution - 0026, Saint Matthews, Kentucky, United States

Local Institution - 0039, Boston, Massachusetts, United States

Local Institution - 0036, Boston, Massachusetts, United States

Local Institution - 0033, Rochester, Minnesota, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

Local Institution - 0034, New Brunswick, New Jersey, United States

Local Institution - 0046, Buffalo, New York, United States

Local Institution - 0002, New York, New York, United States

Local Institution - 0003, New York, New York, United States

Local Institution - 0031, Chapel Hill, North Carolina, United States

Local Institution - 0054, Cincinnati, Ohio, United States

Local Institution - 0032, Columbus, Ohio, United States

Local Institution - 0038, Portland, Oregon, United States

Local Institution - 0043, Nashville, Tennessee, United States

Local Institution - 0035, Dallas, Texas, United States

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Local Institution - 0055, San Antonio, Texas, United States

Local Institution - 0050, Salt Lake City, Utah, United States

Local Institution - 0011, Seattle, Washington, United States

University Hospital and UW Health Clinics, Madison, Wisconsin, United States

Local Institution - 0020, Calgary, Alberta, Canada

Local Institution - 0021, Montréal, Quebec, Canada

Contact Details

Name: Bristol-Myers Squibb

Affiliation: Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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