drugset / Trial / NCT04676529

Study to Evaluate Safety, Pharmacokinetic and Pharmacodynamic Dose Escalation and Expansion Study of PXS-5505 in Patients With Primary, Post-polycythemia Vera or Post-essential Thrombocythemia Myelofibrosis

NCT04676529

Phase 1/2 Completed 43 enrolled Syntara
Non-randomizedSequentialOpen-labelTreatment

Summary

This study will be an open-label phase 1/2a study to evaluate the safety and tolerability of PXS-5505 in patients with primary, postpolycythemia vera (PV) or post-essential thrombocythemia (ET) myelofibrosis.

Timeline

Start
2021-02-18
Primary completion
2025-07-09
Completion
2025-07-09

Drugs

EvaluationDrugModalityDoseRoute
Subject PXS-5505 Unknown 100 mg
Subject PXS-5505 Unknown 200 mg

Indications