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Ruxolitinib

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDDRUG-RUXOLITINIB
TypeDrug
Aliases
JakafiJakaviРуксолітиніб
Statusreviewed 2026-04-25 | pending_clinical_signoff
DiseasesDIS-PMF DIS-PV
SourcesSRC-COMFORT-I-VERSTOVSEK-2012 SRC-NCCN-MPN-2025 SRC-RESPONSE-VANNUCCHI-2015

Drug Facts

ClassJAK1/JAK2 inhibitor
MechanismSelective JAK1/JAK2 inhibitor. Blocks JAK-STAT signaling driven by JAK2 V617F (and CALR/MPL via JAK2 dimerization). Reduces splenomegaly + symptoms in MF/PV/ET; does not eliminate clone. Backbone of MF symptom-driven therapy.
Typical dosingMF: 5-20 mg PO BID by baseline platelet count (plt 50-100K → 5 mg BID; 100-200K → 15 mg BID; >200K → 20 mg BID). Titrate by toxicity. PV (HU-resistant/intolerant): start 10 mg BID; titrate to Hct <45%. GVHD: 5-10 mg BID.
Ukraine registeredTrue
NSZU reimbursedTrue
Ukraine last verified2026-04-27

Warnings

Notes

Established efficacy in symptomatic MF (COMFORT-I/II — improves spleen volume + symptoms + may extend OS in pooled analyses) and HU-resistant PV (RESPONSE — Hct + spleen response). NEVER abrupt-stop — taper over ≥1-2 weeks. HBV / HSV / TB screening before initiation. Anemia is predictable and usually managed with dose modification ± transfusion; momelotinib is preferred if anemia is dominant problem.

Used By

Regimens