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Study details
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A Study of JNJ-90014496 in Participants With B-Cell Non-Hodgkin Lymphoma

Janssen Research & Development, LLC
NCT IDNCT05421663ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

385

Study length

about 6.4 years

Ages

18+

Locations

14 sites in CA, CO, IA +8

What this study is about

This trial is testing a treatment called JNJ-90014496 for people with relapsed or refractory B-cell non-Hodgkin lymphoma. The treatment is an autologous bi-specific chimeric antigen receptor (CAR) T-cell therapy targeting both CD19 and CD20.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive JNJ-90014496

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Phase 1b: Occurrence of Adverse Events (AEs) [Safety and Tolerability], Phase 2: Overall Response (OR) As Assessed by Independent Review Committee (IRC)

Secondary: Change From Baseline of the Functional Assessment of Cancer Therapy-Lymphoma (FACT-Lym) Symptom Score, Phase 1b: Duration of Response (DOR), Phase 1b: Overall Response (OR), Phase 1b: Pharmacokinetic Evaluation of Prizlo-Cel, Phase 2: Area Under the Blood Concentration Time Curve (AUC) for Prizlo-Cel, Phase 2: Complete Response (CR), Phase 2: Duration of Response (DOR), Phase 2: Maximum Observed Blood Concentration (Cmax) for Prizlo-Cel

Body systems

Oncology