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Study identifier: NCT06630104 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Understanding the Mechanisms of Clonal and Non-clonal Cytopenia Following CAR-T Therapy for Multiple Myeloma or CD19+ Lymphoproliferative Disorder (LPD)

Condition: Lymphoproliferative Disorder · Multiple Myeloma  ·  Sponsor: Mayo Clinic

PhaseNA
Planned participants82
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This clinical trial evaluates the impact of preexisting and therapy-emergent germline and somatic variants on cytopenia in patients with multiple myeloma or CD19 positive lymphoproliferative disorder (LPD) following chimeric antigen receptor T-cell (CAR-T) therapy. The most common adverse event after CAR-T therapy is lower than normal blood cells (cytopenia) and up to one third of patients experience cytopenia that last longer than 30 days post-infusion. Germline and somatic variants are changes in genes found using cancer genomic tests. Cancer genetic/genomic testing is a series of tests that find specific changes in cancer cells or in blood deoxyribonucleic acid. Identifying gene mutations may help identify the risk of cytopenia in patients with multiple myeloma or CD19 positive LPD following CAR-T therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Trials Referral Office  ·  855-776-0015  ·  mayocliniccancerstudies@mayo.edu

Always discuss trial participation with your own doctor first.

Locations (7)

Mayo Clinic in ArizonaScottsdale, Arizona, United StatesRecruiting
Mayo Clinic in FloridaJacksonville, Florida, United StatesRecruiting
Mayo Clinic Health System in Albert LeaAlbert Lea, Minnesota, United StatesRecruiting
Mayo Clinic Health System-MankatoMankato, Minnesota, United StatesRecruiting
Mayo Clinic in RochesterRochester, Minnesota, United StatesRecruiting
Mayo Clinic Health System-Eau Claire ClinicEau Claire, Wisconsin, United StatesRecruiting
Mayo Clinic Health System-Franciscan HealthcareLa Crosse, Wisconsin, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06630104