Nivolumab/hyaluronidase

Medication From Wikipedia, the free encyclopedia

Nivolumab/hyaluronidase, sold under the brand name Opdivo Qvantig, is a fixed-dose combination anti-cancer medication used for the treatment of various forms of cancer.[1][2] Nivolumab/hyaluronidase contains nivolumab, a programmed death receptor-1 (PD-1)–blocking monoclonal antibody; and hyaluronidase, an endoglycosidase.[1] It is given by subcutaneous injection.[1][2]

Trade namesOpdivo Qvantig
Other namesNivolumab/hyaluronidase-nvhy
Quick facts Combination of, Hyaluronidase ...
Nivolumab/hyaluronidase
Combination of
NivolumabProgrammed death receptor-1-blocking antibody
HyaluronidaseEndoglycosidase
Clinical data
Trade namesOpdivo Qvantig
Other namesNivolumab/hyaluronidase-nvhy
AHFS/Drugs.comOpdivo-qvantig
MedlinePlusa625029
License data
Routes of
administration
Subcutaneous injection
ATC code
  • None
Legal status
Legal status
Close

Nivolumab/hyaluronidase was approved for medical use in the United States in December 2024.[2]

Medical uses

In December 2024, the US Food and Drug Administration (FDA) approved the combination of nivolumab and hyaluronidase across approved adult, solid tumor nivolumab indications as monotherapy, monotherapy maintenance following completion of hyaluronidase plus ipilimumab combination therapy, or in combination with chemotherapy or cabozantinib.[2] The approval includes indications for renal cell carcinoma, melanoma, non–small cell lung cancer, head and neck squamous cell carcinoma, urothelial carcinoma, colorectal cancer, hepatocellular carcinoma, esophageal carcinoma, gastric cancer, gastroesophageal junction cancer, and esophageal adenocarcinoma.[2]

History

The subcutaneous injection of nivolumab and hyaluronidase was evaluated in CHECKMATE-67T (NCT04810078), a multicenter, randomized, open-label trial in participants with advanced or metastatic clear cell renal cell carcinoma who received no more than two prior systemic treatment regimens.[2] A total of 495 participants were randomized to receive either subcutaneous nivolumab and hyaluronidase or intravenous nivolumab.[2]

Society and culture

Nivolumab/hyaluronidase was approved for medical use in the United States in December 2024.[2][3]

References

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