Skip to content
Study details
Enrolling now

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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Receive JNJ-90014496
PhasePhase 1/Phase 2
Primary goalPhase 1b: Occurrence of Adverse Events (AEs) [Safety and Tolerability]

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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