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Active, not recruiting Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT04245839

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT04245839. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 13, 2026, 3:54 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Open-label, Single Arm, Multicohort, Multicenter Trial to Evaluate the Efficacy and Safety of JCAR017 in Adult Subjects With Relapsed or Refractory Indolent B-cell Non-Hodgkin Lymphoma (NHL)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 follow-up through Day 29; * Posttreatment, which includes follow-up assessments for disease status and safety for 5 years.

Study identification

NCT ID
NCT04245839
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celgene
Industry
Enrollment
276 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 14, 2020 (Actual)
Primary completion
Sep 30, 2031 (Estimated)
Completion
Sep 30, 2031 (Estimated)
Last update posted
Nov 5, 2025

2020 – 2031

United States locations

U.S. sites
23
U.S. states
19
U.S. cities
21
Facility City State ZIP Site status
Local Institution - 111 Santa Monica California 90095 —
Local Institution - 107 Aurora Colorado 80045 —
Local Institution - 105 New Haven Connecticut 06520 —
Local Institution - 103 Chicago Illinois 60611 —
Local Institution - 109 Niles Illinois 60714 —
Local Institution - 122 Iowa City Iowa 52242 —
Local Institution - 124 Wichita Kansas 67124 —
Local Institution - 102 Baltimore Maryland 21201 —
Local Institution - 100 Boston Massachusetts 02114 —
Local Institution - 101 Boston Massachusetts 02215 —
Local Institution - 127 Detroit Michigan 48201 —
Local Institution - 123 Morristown New Jersey 07960 —
Local Institution - 116 New York New York 10021 —
Local Institution - 110 Charlotte North Carolina 28204 —
Local Institution - 112 Cleveland Ohio 44195 —
Local Institution - 114 Portland Oregon 97213 —
Local Institution - 117 Philadelphia Pennsylvania 19104 —
Local Institution - 113 Sioux Falls South Dakota 57105 —
Local Institution - 121 Dallas Texas 75230-2510 —
Local Institution - 104 Houston Texas 77030 —
Local Institution - 119 Houston Texas 77030 —
Local Institution - 115 Charlottesville Virginia 22903 —
Local Institution - 108 Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04245839, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 5, 2025 · Synced Nov 13, 2026

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