Protocol for Transgene Assay Service

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Biological
Study Type: Observational
SUMMARY

The purpose of this transgene assay testing service is to evaluate tumor samples for transgene levels in patients who received a commercially available Bristol-Myers Squibb manufactured gene modified cellular therapy and have reported a qualifying second malignancy.

Eligibility
Participation Requirements
Sex: All
View:

• Participant has received a commercially available Bristol-Myers Squibb (BMS) manufactured Gene Modified Cell Therapy (GMCT) and has been diagnosed with a qualifying second primary malignancy or a second primary malignancy which BMS has qualified for testing.

• Participant has received a commercially available BMS manufactured GMCT in a clinical trial or other investigational setting (including non-conforming product) for which there is no testing protocol in place for that trial or investigational setting and has been diagnosed with a qualifying second primary malignancy or a second primary malignancy which BMS has qualified for testing.

Locations
United States
Texas
Local Institution - 0008
NOT_YET_RECRUITING
Dallas
Utah
Local Institution - 0010
NOT_YET_RECRUITING
Salt Lake City
Wisconsin
Local Institution - 0004
WITHDRAWN
Madison
Other Locations
Germany
Universitaetsklinikum Essen (AoR)
RECRUITING
Essen
Japan
Local Institution - 0003
WITHDRAWN
Kumamoto
Local Institution - 0012
NOT_YET_RECRUITING
Toyokawa
Switzerland
Kantonsspital Aarau
RECRUITING
Aarau
Contact Information
Primary
BMS Study Connect Contact Center www.BMSStudyConnect.com
Clinical.Trials@bms.com
855-907-3286
Backup
First line of the email MUST contain NCT # and Site #.
Time Frame
Start Date: 2023-10-06
Estimated Completion Date: 2038-10-06
Participants
Target number of participants: 50
Treatments
Participants treated with idecabtagene vicleucel
Participants treated with lisocabtagene maraleucel
Related Therapeutic Areas
Sponsors
Leads: Bristol-Myers Squibb

This content was sourced from clinicaltrials.gov