Pembrolizumab
Checkpoint blockade rather than direct cytotoxicity is how pembrolizumab acts: the monoclonal antibody binds programmed cell death protein 1 and prevents the inhibitory signal that tumours exploit to switch off cytotoxic T cells. Releasing that brake restores antitumour immunity, so the therapeutic effect is produced by the patient's own lymphocytes rather than by the drug. The antibody belongs to the antineoplastic and immunomodulating group, and its elimination half-life of roughly 26 days reflects the slow clearance typical of immunoglobulin therapeutics, allowing dosing intervals measured in weeks. Because the mechanism removes an immune restraint, the adverse effects characteristic of the class are autoimmune in nature.
This immunotherapy helps the immune system recognize and attack cancer cells by blocking the PD-1 protein.
Áreas Terapêuticas
Classes de Medicamentos
Mecanismo de Ação
Anti-PD-1 monoclonal antibody restoring anti-tumor immunity.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Anti-PD-1 monoclonal antibody restoring anti-tumor immunity.
HBD / HBA
- / -
Prednisone at immunosuppressive doses may blunt pembrolizumab's anti-tumour efficacy by dampening the T-cell responses required for checkpoint inhibitor activity.
Systemic corticosteroids such as dexamethasone can attenuate pembrolizumab's immune-stimulating anti-tumour activity by suppressing the immune effector responses that the checkpoint inhibitor relies on.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
This immunotherapy helps the immune system recognize and attack cancer cells by blocking the PD-1 protein.
Anti-PD-1 monoclonal antibody restoring anti-tumor immunity.
Key pharmacokinetic parameters for Pembrolizumab: Half-life: 26 days.
Yes, Pembrolizumab is an approved drug. It has reached clinical phase 4. It is classified as a Antibody.
Related Drugs
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3137343. Open-access bioactivity database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.
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