Transgene Assay Testing Service of Tumor Samples From Patients Who Received a Bristol-Myers Squibb Manufactured Gene Modified Cell Therapy and Have a Qualifying Second Primary Malignancy
Condition(s) studied
Investigational drug(s) / intervention(s)
Idecabtagene vicleucel: As per product label
Lisocabtagene maraleucel: As per product label
Study 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
Primary outcome measure(s)
- Participant in situ hybridization (ISH) or droplet-based digital Polymerase chain reaction (ddPCR) transgene testing results — Baseline
- Participant insertion site analysis (ISA) testing results — Baseline
For participants with positive in situ hybridization (ISH) transgene or droplet-based digital polymerase chain reaction (ddPCR) transgene
Trial sites (8)
| Facility | City | Region | Status |
|---|---|---|---|
| Local Institution - 0016 | Portland | Oregon | Not Yet Recruiting |
| Ut Southwestern | Dallas | Texas | Recruiting |
| Huntsman Cancer Institute at the University of Utah | Salt Lake City | Utah | Recruiting |
| Local Institution - 0004 | Madison | Wisconsin | Withdrawn |
| Universitaetsklinikum Essen (AoR) | Essen | Germany | Recruiting |
| Toyokawa City Hospital | Toyokawa | Aichi-ken | Recruiting |
| Local Institution - 0003 | Kumamoto | Kumamoto | Withdrawn |
| Kantonsspital Aarau | Aarau | Switzerland | Recruiting |
More Bristol-Myers Squibb trials in Japan
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06357754 on ClinicalTrials.gov ↗ ← All trials in Japan