A Single-arm Prospective Study of Secondary Infusion of Relmacabtagene Autoleucel Injection for Relapsed or Refractory B-cell Lymphoma

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

To observe the efficacy and safety of a second infusion of relma-cel injection in patients with relapsed or refractory B-cell lymphoma.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• Patients have signed an Informed Consent Form (ICF).

• Adults diagnosed with relapsed or refractory B-cell lymphoma who have completed initial treatment with Relma-cel.

• Patients must have undergone at least one disease assessment post-initial Relma-cel treatment, and the investigator decides to administer a second treatment (including PR/PD/SD) based on clinical practice.

• Before the second infusion, confirm that the prepared dose of relma-cel is sufficient (recommended 80-150 x 10\^6 CAR-T cells), with specific dosage determined by the investigator based on patient condition and dose availability.

• Confirm the presence of CD19+ residual tumor tissue, if clinically permissible.

• Measure plasma for the absence of anti-drug antibodies (ADA) to relma-cel before the second treatment.

• Toxicity related to lymphodepleting chemotherapy (fludarabine and cyclophosphamide), except for hair loss, must have resolved to ≤ Grade 1 or returned to baseline levels before retreatment.

• Patients must not have experienced severe adverse reactions during the first treatment, or any adverse reactions must have resolved to baseline levels from the first treatment.

Locations
Other Locations
China
NO.197, Ruijin Er Road
RECRUITING
Shanghai
Contact Information
Primary
Weili Zhao, professor
zwl_trial@163.com
+86 021-64370045
Time Frame
Start Date: 2023-05-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 8
Treatments
Experimental: Relma-cel secondary infusion
Related Therapeutic Areas
Sponsors
Leads: Ruijin Hospital

This content was sourced from clinicaltrials.gov