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A Phase 2, Open Label, Multiple Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Voxelotor in Patients With Sickle Cell Disease

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Trial Profile

A Phase 2, Open Label, Multiple Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Voxelotor in Patients With Sickle Cell Disease

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 24 Nov 2023

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At a glance

  • Drugs Voxelotor (Primary)
  • Indications Sickle cell anaemia
  • Focus Adverse reactions
  • Sponsors Pfizer

Most Recent Events

  • 01 Nov 2023 Timeline for the primary end-point is increased from 200 days to 300 days.
  • 29 Aug 2022 Status changed from recruiting to discontinued.
  • 04 Feb 2020 New trial record

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