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64Cu-GRIP B

Development stage
Phase 2
Lead developer
University of California, San Francisco
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Peptide-Drug Conjugates → Peptide Conjugates → Peptides
Administration
Intravenous
01

Overview

64Cu-GRIP B is a diagnostic radiopharmaceutical and peptide conjugate radionuclide designed for positron emission tomography (PET) imaging. It specifically targets extracellular granzyme B, an enzyme secreted by activated immune cells in the tumor microenvironment, particularly following immunotherapy such as immune checkpoint inhibitors or CAR-T cell therapy. The drug consists of a peptide substrate optimized for cleavage by human granzyme B, conjugated to DOTA and radiolabeled with copper-64. Upon systemic administration, the inactive pro-form of the probe is cleaved by extracellular granzyme B at sites of immune activation, releasing a radiolabeled antimicrobial peptide that binds to nearby cell membranes—enabling visualization of active anti-tumor immunity via PET imaging. This mechanism allows noninvasive assessment of immune response within tumors and may help predict or monitor responses to immunomodulatory therapies in cancer patients[1][2][5][6].

Other names
64Cu-GRIP BCopper-64 granzyme targeting restricted interaction peptide specific to family member BCopper64 granzyme targeting restricted interaction peptide specific to family member BCopper 64 granzyme targeting restricted interaction peptide specific to family member B
02

Targets

GZMB (Granzyme B)

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