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Recruiting NCT06357754

NCT06357754 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

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Clinical Trial Summary
NCT ID NCT06357754
Status Recruiting
Phase
Sponsor Bristol-Myers Squibb
Condition Non-Hodgkin Lymphoma
Study Type OBSERVATIONAL
Enrollment 50 participants
Start Date 2023-10-06
Primary Completion 2038-10-06

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Idecabtagene vicleucelLisocabtagene maraleucel

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 50 participants in total. It began in 2023-10-06 with a primary completion date of 2038-10-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

Inclusion Criteria: * 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. Exclusion Criteria: * Participant is actively participating in a clinical trial where information and sample collection is being conducted under that clinical trial. * Participant has not received a BMS manufactured GMCT or has not been diagnosed with a qualifying second primary malignancy.

Contact & Investigator

Central Contact

BMS Study Connect Contact Center www.BMSStudyConnect.com

✉ Clinical.Trials@bms.com

📞 855-907-3286

Principal Investigator

Bristol-Myers Squibb

STUDY DIRECTOR

Bristol-Myers Squibb

Frequently Asked Questions

Who can join the NCT06357754 clinical trial?

This trial is open to participants of all sexes, studying Non-Hodgkin Lymphoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06357754 currently recruiting?

Yes, NCT06357754 is actively recruiting participants. Contact the research team at Clinical.Trials@bms.com for enrollment information.

Where is the NCT06357754 trial being conducted?

This trial is being conducted at Portland, United States, Dallas, United States, Salt Lake City, United States, Madison, United States and 4 additional locations.

Who is sponsoring the NCT06357754 clinical trial?

NCT06357754 is sponsored by Bristol-Myers Squibb. The principal investigator is Bristol-Myers Squibb at Bristol-Myers Squibb. The trial plans to enroll 50 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology