A Study of JNJ-90009530 in Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma (r/r B-NHL)

Last updated: September 24, 2026
Sponsor: Janssen Research & Development, LLC
Overall Status: Active - Not Recruiting

Phase

1

Condition

Lymphoma

Lymphoma, B-cell

Treatment

JNJ-90009530

C-CAR066

Clinical Study ID

NCT05784441
90009530LYM1001
2023
90009530LYM1001
2023-506259-97-00
  • Ages > 18
  • All Genders

Study Summary

The goal of this multicenter study is to test JNJ-90009530 in Relapsed or Refractory Non-Hodgkin Lymphoma Patients. The main questions the study aims to answer are:

  • can a dose of JNJ-90009530 be determined that is safe and well tolerated by patients.

  • will JNJ-90009530 help patients achieve a response and for how long?

Eligibility Criteria

Inclusion

Key Inclusion Criteria

  • Participant must be greater than or equal to (>=) 18 years of age, at the time of signing informed consent

  • All participants must have relapsed or refractory disease for each histologic subtype

  • Mature aggressive large B cell NHL and Follicular Lymphoma Grade 3b: Participants must have >= 2 lines of systemic therapy or >=1 line of systemic therapy in case of participants ineligible for high-dose chemotherapy and autologous Hematopoietic stem cell transplantation (HSCT). Participants also must have had exposure to an anthracycline and an anti-CD20 targeted agent

  • 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

  • Tumor must be cluster of differentiation (CD) 20 positive

  • Measurable disease as defined by Lugano 2014 classification

  • Eastern Cooperative Oncology Group (ECOG) performance status of either 0 or 1

Key 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, 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

  • Active central nervous system (CNS) involvement by malignancy

  • Current active liver or biliary disease (except for Gilbert's syndrome or asymptomatic gallstones)

Study Design

Total Participants: 21
Treatment Group(s): 2
Primary Treatment: JNJ-90009530
Phase: 1
Study Start date:
November 06, 2023
Estimated Completion Date:
January 03, 2040

Connect with a study center

  • Royal Prince Alfred Hospital

    Camperdown, 2050
    Australia

    Site Not Available

  • Monash Medical Centre

    Clayton, 3168
    Australia

    Site Not Available

  • Austin Hospital

    Heidelberg, 3084
    Australia

    Site Not Available

  • Royal Brisbane and Women's Hospital

    Herston, 4029
    Australia

    Site Not Available

  • Westmead Hospital

    Westmead, 2145
    Australia

    Site Not Available

  • Hadassah Medical Center

    Jerusalem, 9112001
    Israel

    Site Not Available

  • Sheba Medical Center

    Ramat Gan, 5266202
    Israel

    Site Not Available

  • University College London Hospitals

    London, NW1 2BU
    United Kingdom

    Site Not Available

  • University of Iowa Hospital

    Iowa City, Iowa 52242
    United States

    Site Not Available

  • University of Kentucky

    Lexington, Kentucky 40506
    United States

    Site Not Available

  • Mayo Clinic Rochester

    Rochester, Minnesota 55905
    United States

    Site Not Available

  • Rutgers University

    New Brunswick, New Jersey 08901
    United States

    Site Not Available

  • University Hospitals Cleveland Medical Center

    Cleveland, Ohio 44106
    United States

    Site Not Available

  • University of Pennsylvania

    Philadelphia, Pennsylvania 19104
    United States

    Site Not Available

  • MD Anderson Cancer Center

    Houston, Texas 77030
    United States

    Site Not Available

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