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KEYTRUDA QLEX (BERAHYALURONIDASE ALFA-PMPH)

MERCK SHARP DOHME · FDA-approved approved Quality 6/100

KEYTRUDA QLEX (generic name: BERAHYALURONIDASE ALFA-PMPH) is a Programmed Death Receptor-1 Blocking Antibody [EPC] drug developed by MERCK SHARP DOHME. It is currently FDA-approved.

At a glance

Generic nameBERAHYALURONIDASE ALFA-PMPH
SponsorMERCK SHARP DOHME
Drug classProgrammed Death Receptor-1 Blocking Antibody [EPC]
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

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

Competitive intelligence

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Frequently asked questions about KEYTRUDA QLEX

What is KEYTRUDA QLEX?

KEYTRUDA QLEX (BERAHYALURONIDASE ALFA-PMPH) is a Programmed Death Receptor-1 Blocking Antibody [EPC] drug developed by MERCK SHARP DOHME.

Who makes KEYTRUDA QLEX?

KEYTRUDA QLEX is developed and marketed by MERCK SHARP DOHME (see full MERCK SHARP DOHME pipeline at /company/merck).

What is the generic name of KEYTRUDA QLEX?

BERAHYALURONIDASE ALFA-PMPH is the generic (nonproprietary) name of KEYTRUDA QLEX.

What drug class is KEYTRUDA QLEX in?

KEYTRUDA QLEX 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 KEYTRUDA QLEX in?

KEYTRUDA QLEX is FDA-approved (marketed).

What are the side effects of KEYTRUDA QLEX?

Common side effects of KEYTRUDA QLEX include Nausea, Fatigue, Musculoskeletal pain.

Related

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