Essential Thrombocythemia
Percentage of patients achieving a reduction of platelet counts to ≤400x109/L in the absence of any subsequent thrombotic events while maintaining normal platelet counts, at any time during 24 weeks of treatment, Occurrence, severity of Treatment Emergent Adverse Events (TEAEs) (graded using the Common Terminology Criteria for AEs -CTCAE) v 5.0 criteria
This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View 2025-523864-19-00 on CTIS ↗ ← All trials in the EU