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临床试验/PACTR202209867711506
PACTR202209867711506尚未招募3 期

An Open-Label Extension Study of Voxelotor Administered Orally to Pediatric Participants with Sickle Cell Disease Who Have Participated in Voxelotor Clinical Trials

Global Blood Therapeutics inc0 个研究点目标入组 300 人开始时间: 2022年7月6日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
1 Month(s) 至 23 Month(s)(—)
性别
All

入选标准

  • 1. Male or female participant with SCD, up to 18 years, who participated and received study drug in a GBT-sponsored voxelotor pediatric clinical study
  • 2. Participant has provided written assent (both the consent of the participant's legal representative or legal guardian and the participant's assent [where applicable] must be obtained)

排除标准

  • 1.Female participant who is breastfeeding or pregnant
  • 2. Participant withdrew consent from a GBT-sponsored voxelotor pediatric clinical study
  • 3. Known hypersensitivity to voxelotor or any other components of the study drug

研究者

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