drugset / Trial / NCT02631044

Study Evaluating the Safety and Pharmacokinetics of JCAR017 in B-cell Non-Hodgkin Lymphoma (TRANSCEND-NHL-001)

NCT02631044 ↗

Phase 1 Completed 387 enrolled Juno Therapeutics, a Subsidiary of Celgene
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This open-label Phase 1 study will evaluate the safety, PK, and antitumor activity of modified T cells (JCAR017) administered to adult patients with relapsed or refractory B-cell NHL. The dose and schedule of JCAR017 will be evaluated and modified, as needed, for safety and antitumor activity. We will also determine how long the modified T cells stay in the patient's body and how well JCAR017 works in treating patients with non-Hodgkin's lymphoma whose disease has come back or has not responded to treatment.

Timeline

Start
2016-01-06
Primary completion
2024-05-16
Completion
2024-05-16

Outcome

Met primary endpoint

release “(TRANSCEND NHL 001) met its primary and secondary endpoints” bms.com ↗

release “With a median on-study follow-up of 16.1 months, the ORR in patients evaluated for efficacy in the primary analysis set (n=74) was 86.5% (95% CI: 76.5-93.3; one-sided p<0.0001)” bms.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lisocabtagene Maraleucel Cell therapy 5e+07 cells Intravenous
Subject Lisocabtagene Maraleucel Cell therapy 1e+08 cells Intravenous
Subject Lisocabtagene Maraleucel Cell therapy 1.5e+08 cells Intravenous