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Clinical Trials in the EU / 2025-523864-19-00
Completed Phase II

Phase 2 study of iadademstat for the treatment of patients with essential thrombocythemia resistant/intolerant to hydroxyurea

2025-523864-19-00 · tracked via the Priya Life Science EU tracker
Sponsor
Oryzon Genomics S.A.
Sponsor type
Pharmaceutical company
Therapeutic area
Hemic and Lymphatic Diseases
Decision date
20/02/2026
Enrollment target
36
Sites
Spain

Condition studied

Essential Thrombocythemia

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

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

Official registry record

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