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OPDIVO QVANTIG (HYALURONIDASE-NVHY)

BRISTOL-MYERS SQUIBB · FDA-approved approved Quality 6/100

OPDIVO QVANTIG (generic name: HYALURONIDASE-NVHY) is a Programmed Death Receptor-1 Blocking Antibody [EPC] drug developed by BRISTOL-MYERS SQUIBB. It is currently FDA-approved.

At a glance

Generic nameHYALURONIDASE-NVHY
SponsorBRISTOL-MYERS SQUIBB
Drug classProgrammed Death Receptor-1 Blocking Antibody [EPC]
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about OPDIVO QVANTIG

What is OPDIVO QVANTIG?

OPDIVO QVANTIG (HYALURONIDASE-NVHY) is a Programmed Death Receptor-1 Blocking Antibody [EPC] drug developed by BRISTOL-MYERS SQUIBB.

Who makes OPDIVO QVANTIG?

OPDIVO QVANTIG is developed and marketed by BRISTOL-MYERS SQUIBB (see full BRISTOL-MYERS SQUIBB pipeline at /company/bristol-myers-squibb).

What is the generic name of OPDIVO QVANTIG?

HYALURONIDASE-NVHY is the generic (nonproprietary) name of OPDIVO QVANTIG.

What drug class is OPDIVO QVANTIG in?

OPDIVO QVANTIG belongs to the Programmed Death Receptor-1 Blocking Antibody [EPC] class. See all Programmed Death Receptor-1 Blocking Antibody [EPC] drugs at /class/programmed-death-receptor-1-blocking-antibody-epc.

What development phase is OPDIVO QVANTIG in?

OPDIVO QVANTIG is FDA-approved (marketed).

What are the side effects of OPDIVO QVANTIG?

Common side effects of OPDIVO QVANTIG include Musculoskeletal pain, Fatigue, Pruritus, Rash, Hypothyroidism, Diarrhea. Serious adverse events: Serious adverse reactions (overall), Pleural effusion, Pneumonitis, Hyperglycemia.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing