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By physician referral or invitation only

Multiple Myeloma study

You are being asked to take part in this study because you previously agreed to receive a U.S. Food and Drug Administration (FDA) approved drug, idecabtagene vicleucel (ide-cel), for the treatment of your disease as part of routine care and not a clinical research study. You had the blood collection (leukapheresis) (pronounced loo-ka-fer-ee-sis) procedure, your T cells (a subset of your white blood cells that are part of your immune system and attack things like infections and cancer cells) were collected and genetically modified in a laboratory in order to manufacture the ide-cel T cells for your disease treatment. The ide-cel T cells that were produced do not meet all of the prespecified release criteria to be used as a routine prescription drug as required by the governing health authority (such as the FDA) where you are being treated. For example, the modified T cells may have a lower cell

Age & Gender

  • 18 years ~ 99 years
  • Male, Female, Gender Inclusive

Contact the Team

Location

Thank you for your interest, but this study is recruiting by invitation only.

North Carolina (Statewide)

Additional Study Information

Principal Investigator

Sascha Tuchman
LCCC - Clinical Trials

Study Type

Clinical or Medical
Interventional

Study Topics

Blood Conditions

IRB Number

20-2838

ClinicalTrials.gov

NCT04771078

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