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Camrelizumab

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IDDRUG-CAMRELIZUMAB
TipoFármaco
Alegais
AíRuiKaSHR-1210Камрелізумаб
Estadoreviewed 2026-07-11 | pending_clinical_signoff
DoençasDIS-NPC
FontesSRC-CAPTAIN-1ST-YANG-2021

Fatos sobre as drogas

ClasseAnti-PD-1 humanizado anticorpo monoclonal IgG4 (inibidor do ponto de controlo imune)
MecanismoHumanized IgG4 monoclonal antibody binding PD-1 on activated T cells, blocking PD-1/PD-L1 and PD-1/PD-L2 interactions and restoring cytotoxic T-cell antitumor activity. Same general anti-PD-1 mechanistic class as pembrolizumab, nivolumab, and toripalimab. Studied specifically in recurrent/metastatic nasopharyngeal carcinoma (CAPTAIN-1st) combined with gemcitabine + cisplatin, as well as in multiple other Chinese-registered indications (hepatocellular carcinoma, NSCLC, esophageal SCC, classical Hodgkin lymphoma).
Dose típicaPer the CAPTAIN-1st trial protocol: camrelizumab 200 mg IV every 3 weeks, combined with gemcitabine + cisplatin (GP) for up to 6 cycles, followed by camrelizumab monotherapy (200 mg IV q3w) until disease progression, unacceptable toxicity, or up to 2 years total. STUB — dosing drafted from trial-protocol recall; pending Clinical Co-Lead confirmation against the primary source.
Ucrânia registadaFalso
NSZU reembolsadoFalso

Notas

STUB — draft entity pending Clinical Co-Lead sign-off (CHARTER §6.1; currently dev-mode-exempted). Anti-PD-1 backbone alternative for NPC metastatic 1L combination per CAPTAIN-1st (Yang Y et al., Lancet Oncol 2021): camrelizumab + gemcitabine + cisplatin significantly improved PFS vs chemo alone in treatment-naive recurrent/metastatic NPC. NOT FDA-approved (China/NMPA-approved only) — distinguishes it from toripalimab (DRUG-TORIPALIMAB), the FDA-approved alternative for the identical clinical scenario. Reuse this entity rather than duplicate. RCCEP is a genuinely distinctive camrelizumab-class AE not shared with pembrolizumab/nivolumab/toripalimab — worth flagging for patient counseling.

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