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A Study to Evaluate the Efficacy and Safety of JCAR017 in Adult Subjects With Relapsed or Refractory Indolent B-cell Non-Hodgkin Lymphoma (NHL)

Active, not recruiting · Phase 2 · NCT04245839

Conditions: Lymphoma, Non-Hodgkin

At a glance

Research payments reported, 2025
$2.6M
U.S. investigators named
19
Sites paid
19
Planned or actual enrollment
276

About the trial

Sponsor
Celgene
Tested
Fludarabine (drug), Cyclophosphamide (drug), JCAR017 (drug)
Dates
Started 2020-07-14; completion 2031-09-30
Results posted
Not yet

This is a global Phase 2, open-label, single-arm, multicohort, multicenter study to evaluate efficacy and safety of JCAR017 in adult subjects with r/r FL or MZL. The study will be conducted in compliance with the International Council on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use/Good Clinical Practice (GCP) and applicable regulatory requirements. This study is divided into three periods: * Pretreatment, which consists of screening assessments, leukapheresis and the Pretreatment evaluation; * Treatment, which starts with the administration of lymphodepleting (LD) chemotherapy and continues through JCAR017 administration at Day 1 with fo…

From ClinicalTrials.gov, last updated 2025-11-05. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Celgene Corporation reported $2.6M in research payments for this study in 2025 (19 payments).

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.