Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at San Francisco, California and other locations
Dates
study started

Description

Summary

This study is designed to evaluate the safety and efficacy of nonconforming idecabtagene vicleucel (ide-cel) in participants with multiple myeloma per the approved prescribing information. This is an expanded access protocol (EAP) to be conducted at Risk Evaluation and Mitigation Strategies (REMS) qualified sites approved for commercial administration of idecabtagene vicleucel and where the EAP is authorized to be conducted for use of nonconforming idecabtagene vicleucel. Non-conforming idecabtagene vicluecel is idecabtagene vicleucel that does not meet commercial release specifications but may be acceptable for use as an investigational product in the Expanded Access Protocol setting.

Official Title

Expanded Access Protocol (EAP) for Subjects Receiving Idecabtagene Vicleucel That is Nonconforming for Commercial Release

Keywords

Multiple Myeloma BB2121 Expanded Access idecabtagene vicleucel nonconforming CAR T EAP Pre-Approval Access Nonconforming idecabtagene vicleucel

Eligibility

You can join if…

Open to people ages 18 years and up

  • Had a participant-specific batch of Idecabtagene vicleucel (ide-cel) manufactured intended for commercial treatment; however, the final manufactured product was nonconforming and did not meet commercial release criteria
  • Remanufacturing is deemed not feasible or clinically inappropriate per assessment of the treating physician in discussion with the participant
  • Clinically stable

You CAN'T join if...

  • Has a hypersensitivity to the active substance or to any of the excipients
  • No experience of a significant worsening in clinical status that would, in the opinion of the treating physician, either increase the risk of Adverse Events associated with lymphodepleting chemotherapy, or exclude them from treatment with nonconforming Idecabtagene vicleucel (ide-cel)
  • Has any condition and/or laboratory abnormality that places the participant at unacceptable risk if he/she were to participate in the Expanded Access Protocol based on the Investigator's judgement

Other protocol-defined inclusion/exclusion criteria apply

Locations

  • University of California San Francisco Medical Center not accepting new patients
    San Francisco California 94142 United States
  • Stanford University not accepting new patients
    Stanford California 94305 United States

Details

Status
not accepting new patients
Start Date
Sponsor
Celgene
Links
EAP Investigator Requests BMS Clinical Trial Information FDA Safety Alerts and Recalls BMS Clinical Trial Patient Recruiting
ID
NCT04771078
Study Type
Expanded Access
Last Updated