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A Phase Ib Multicenter, Open-Label, Study of JNJ-90014496, an Autologous CD19/CD20 Bi-specific CAR-T Cell Therapy in Adult Participants With Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma


Description

This is a Phase Ib multicenter, open-label study of JNJ-90014496, an autologous bi-specific chimeric antigen receptor (CAR) T-cell therapy, targeting both cluster of differentiation (CD) CD19 and CD20 for the treatment of adult participants with relapsed or refractory B-Cell non-Hodgkin lymphoma (r/r B-NHL).

Trial Eligibility

* Participant must be greater than or equal to (\>=) 18 years of age, at the time of signing informed consent * Diagnosis of mature aggressive large B cell non-Hodgkin lymphoma or follicular lymphoma * Tumor must be histologically confirmed cluster of differentiation (CD)19 and/or CD20 positive * Must have relapsed or refractory disease with the following indications for each histologic subtype: Mature aggressive large B cell non-Hodgkin lymphoma (NHL) and follicular lymphoma Grade 3b: Participants must have \>= 2 lines of systemic therapy, or \>= 1 line of systemic therapy for participants who are ineligible for autologous stem cell transplant; Follicular lymphoma Grade 1-3a and marginal zone lymphoma: Participants must have \>= 2 prior lines of anti-neoplastic systemic therapy. Participants also must have prior exposure to an anti-CD20 monoclonal antibody * Measurable disease as defined by Lugano 2014 classification * Eastern cooperative oncology group (ECOG) performance status of either 0 or 1 Exclusion Criteria * Diagnosis of Human herpes virus (HHV) 8-positive diffuse large B Cell lymphoma (DLBCL) * Prior allogeneic hematopoietic stem cell transplantation (HSCT) * Autologous stem cell transplant within 12 weeks of chimeric antigen receptor (CAR) T cell infusion * Uncontrolled active infections * History of deep vein thrombosis or pulmonary embolism within six months of infusion (except for line associated deep vein thrombosis \[DVT\]) * History of stroke, unstable angina, myocardial infarction, congestive heart failure New York Heart Association (NYHA) Class III or IV, severe cardiomyopathy or ventricular arrhythmia requiring medication or mechanical control within 6 months of screening * History of a seizure disorder, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease or neurodegenerative disorder * Known history or prior diagnosis of optic neuritis or other immunologic or inflammatory disease affecting the central nervous system * Current active liver or biliary disease (except for Gilbert's syndrome or asymptomatic gallstones)

Study Info

Organization

Janssen Research & Development, LLC


Primary Outcome

Occurrence of Adverse Events (AEs) [Safety and Tolerability]


Outcome Timeframe Up to 24 months

NCTID NCT05421663

Phases PHASE1

Primary Purpose TREATMENT

Start Date 2022-08-12

Completion Date 2026-05-29

Enrollment Target 104

Interventions

BIOLOGICAL JNJ-90014496

Locations Recruiting

City of Hope

United States, California, Duarte


Colorado Blood Cancer Institute

United States, Colorado, Denver


University of Iowa Hospital and Clinics

United States, Iowa, Iowa City


Rutgers Cancer Institute of New Jersey

United States, New Jersey, Piscataway


Levine Cancer Institute

United States, North Carolina, Charlotte


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