PET Imaging Study of 64Cu-GRIP B for Patients Receiving CD19-directed CAR-T Therapy

Official title

A Phase I/Ib PET Imaging Study of 64Cu-GRIP B, a Radiotracer Targeting Granzyme B, in Patients Receiving CD19-directed CAR-T Therapy

Overview

This is a phase I/Ib imaging study of granzyme B, 64-copper granzyme targeting restricted interaction peptide specific to family member B (64Cu-GRIP B) Positron Emission Tomography (PET) in patients with relapsed/refractory non-Hodgkin's lymphoma (NHL) receiving CD19-directed Chimeric antigen receptor T cells (CAR-T) therapy. The proposed study represents the first-ever lymphoma patient imaging studies with 64Cu-GRIP B PET. The tracer is designed to detect extracellular granzyme B as it is secreted by activated immune cells in the tumor microenvironment, which may highlight tumors that will exhibit a durable response to Cluster of Differentiation 19 (CD19)-directed CAR T-cell therapy.

Detailed description

Primary Objectives:

1\. To establish the feasibility of granzyme B detection with 64Cu-GRIP B PET in participants with relapsed/refractory NHL receiving CD19-directed CAR-T cell therapy in both cohorts.

Secondary Objectives:

1. To descriptively report the patterns of intra-tumoral uptake of 64Cu-GRIP B on whole body PET, including by site of disease, uptake by tumor type, inter-tumoral and inter-participant heterogeneity, and tumor-to-background signal in participants with participants with NHL. 2. To descriptively report the number of lesions identified on 64Cu-GRIP B PET compared with conventional imaging in participants with NHL. 3. To assess the safety of 64Cu-GRIP B in participants with NHL undergoing CAR-T cell therapy.

Participants will be initially enrolled in Cohort 1. Based on the interim analysis, enrollment will begin in Cohort 2. An optional research biopsy will be collected after the post-therapy scan and participants will be followed for 12 months after the end of the study intervention.

Interventions

• Drug 64Cu-GRIP B
  Given IV
• Procedure Positron Emission Tomography (PET)
  Undergo imaging procedure
• Procedure Optional tumor biopsy
  Undergo optional tumor biopsy

Primary outcome measures

• Proportion of positive tumors at the post-CAR-T scan [Time frame: From prior to CAR-T to Day 22 following CAR-T cell, approximately 32 days total]

Secondary outcome measures (4)

• Mean SUVmax by disease site [Time frame: From prior to CAR-T to Day 22 following CAR-T cell, approximately 32 days total]
• Overall Mean SUVmax by cohort [Time frame: From prior to CAR-T to Day 22 following CAR-T cell, approximately 32 days total]
• Percent of lymphoma lesions detected [Time frame: From prior to CAR-T to Day 22 following CAR-T cell, approximately 32 days total]
• Frequency and severity of treatment-emergent adverse events [Time frame: Up to 13 months]

Eligibility criteria

Inclusion criteria

• Disease characteristics, as defined by:

• Histologically-confirmed relapsed/refractory non-Hodgkin lymphoma (NHL) with at least one prior line of therapy.
• Planned treatment with a commercially available CD19 targeting CAR-T cell product.
• Willing to undergo post-treatment tumor biopsies and has safely accessible soft tissue lesion.
• Age >= 18 years.
• Ability to understand and the willingness to sign a written informed consent document.
• Eastern Cooperative Oncology Group (ECOG) performance status <2 (Karnofsky >60%).
• Individuals with treated brain metastases are eligible if follow-up brain imaging after central nervous system (CNS)-directed therapy shows no evidence of progression.
• Individuals with new or progressive brain metastases (active brain metastases) or leptomeningeal disease are eligible if the treating physician determines that immediate CNS specific treatment is not required and is unlikely to be required during the first cycle of therapy.
• Individuals with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial. The effects of 64Cu-GRIP B on the developing human fetus are unknown. For this reason, participants of childbearing potential must agree to use adequate contraception: all participants should use barrier protection for the duration of study participation and for one month after last administration of study intervention. Should a participant become pregnant or suspect they are pregnant while they or their partner are participating in this study, they should inform their treating physician immediately. Male participants treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of study participation, and one month after last administration of study treatment.

Exclusion criteria

• Any condition that, in the opinion of the Principal Investigator, would impair the participant's ability to comply with study procedures.
• Pregnant participants are excluded from this study because the effects of 64Cu-GRIP B on the developing human fetus are unknown. There is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the nursing parent with 64Cu-GRIP B, breastfeeding should be discontinued if the nursing parent receives 64Cu-GRIP B.
• Hypersensitivity to 64Cu-GRIP B or any of its excipients.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation

Non-randomized

Model

Sequential

Masking

Open label

Primary purpose

Diagnostic

Study locations

United States · 1 center

• University of California, San Francisco — San Francisco

Identifiers

NCT: NCT06522932 · 24923 · NCI-2024-05085

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗