drugset / Trial / NCT04247594

Dose Escalation Study to Evaluate the Safety, Tolerability, PK and PD of Voxelotor in Patients With SCD

NCT04247594

Phase 2 Terminated 6 enrolled Pfizer
Non-randomizedSequentialOpen-labelTreatment

Summary

Study participants will undergo up to four periods of voxelotor administered orally at progressively higher dose levels from 1500 mg until either a maximum tolerated dose (MTD) or 3000 mg/day dose is reached, whichever occurs first

Timeline

Start
2020-01-09
Primary completion
2021-06-08
Completion
2021-06-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Voxelotor Small molecule 3000 mg Oral

Indications