Drug intelligence / Profile preview

nivolumab + hyaluronidase-nvhy

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Recombinant Proteins and Enzymes
Administration
Subcutaneous
01

Overview

Nivolumab + hyaluronidase-nvhy (Opdivo Qvantig) is a subcutaneous coformulation developed by Bristol Myers Squibb. It combines nivolumab, a fully human IgG4 monoclonal antibody targeting the programmed cell death receptor-1 (PD-1), with recombinant human hyaluronidase-nvhy, an enzyme that facilitates drug absorption by degrading hyaluronic acid in the subcutaneous extracellular matrix. By blocking the PD-1 receptor on T-cells, nivolumab prevents tumor-expressed PD-L1 and PD-L2 from suppressing the immune response, thereby restoring the immune system's ability to attack cancer cells. Approved by the FDA in December 2024, this formulation allows for a 3–5 minute subcutaneous injection, providing a more convenient alternative to the intravenous administration of nivolumab across various solid tumor indications, including melanoma, non-small cell lung cancer, and renal cell carcinoma.

Brand names
Opdivo Qvantig
Other names
nivolumab and hyaluronidase-nvhy
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)

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