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Pembrolizumab

KEYTRUDA

What it isPD-1 blocking antibody releasing T-cell inhibition; melanoma, lung cancer and many tumors with high PD-L1 or MSI.

Why this oneIt pioneered tumor-agnostic immunotherapy for MSI-high cancers and now carries an exceptionally broad oncology label.

What limits itImmune-related adverse events can hit any organ — thyroid, colon, liver, lung, pituitary — and are treated with steroids, not by stopping alone.

FDA label

FDA dosingPopulationStartTargetMax
Solid tumors and lymphomas (multiple approved indications)adults200 mg IV every 3 weeks or 400 mg IV every 6 weeks200 mg Q3W or 400 mg Q6W400 mg Q6W
Pediatric-approved indications (e.g., melanoma, cHL, PMBCL, MCC, MSI-H/dMMR, TMB-H)pediatric2 mg/kg (up to 200 mg) IV every 3 weeks2 mg/kg (up to 200 mg) Q3W200 mg per dose

Renal Undefined

Hepatic Undefined

Regimen and combination partners vary by indication (see full prescribing information).

Instructions

Cautions

Adverse reactions

Pregnancy Can cause fetal harm based on mechanism of action; advise of risk to a fetus.

Lactation No data on presence in milk; do not breastfeed during treatment and for 4 months after the last dose.

NO BOXED WARNINGS

Principal riskImmune-related adverse events in any organ

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

Mechanism of action: Pembrolizumab ballicule

Pembrolizumab ballicule: receptor binding, kinetics and half-life diagram

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Memory aids: mascots and interaction avatars

Pembrolizumab KEYTRUDA mascot mnemonic cartoon
“Key Pimp bro”

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