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A Study to Compare the Efficacy and Safety of JCAR017 to Standard of Care in Adult Subjects With High-risk, Transplant-eligible Relapsed or Refractory Aggressive B-cell Non-Hodgkin Lymphomas

Completed · Phase 3 · NCT03575351

Conditions: Lymphoma, Non-Hodgkin

At a glance

Research payments reported, 2025
$57,544
U.S. investigators named
2
Sites paid
2
Planned or actual enrollment
184

About the trial

Sponsor
Celgene
Tested
Standard of Care (drug), JCAR017 (genetic)
Dates
Started 2018-10-23; completion 2023-10-23
Results posted
Yes

The study will be conducted in compliance with the International Council for Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use/Good Clinical Practice (GCP) and applicable regulatory requirements. This is a randomized, open-label, parallel-group, multi-center trial in adult subjects with Relapsed or refractory (R/R) aggressive Non-Hodgkin lymphoma (NHL) to compare safety and efficacy between the standard of care (SOC) strategy versus JCAR017 (also known as lisocabtagene maraleucel or liso-cel). Subjects will be randomized to either receive SOC (Arm A) or to receive JCAR017 (Arm B). All subjects randomized to Arm A will receive Standard of care …

From ClinicalTrials.gov, last updated 2025-08-03. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Celgene Corporation reported $57,544 in research payments for this study in 2025 (2 payments).

Products named: Imfinzi

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.