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临床试验/CTIS2023-508735-31-00
CTIS2023-508735-31-00进行中(未招募)1 期

IMPAHCT-FUL: A Long-Term Extension, Multi-Center Safety Study of AV-101 in Subjects With Pulmonary Arterial Hypertension (PAH) Who Have Completed Study AV-101-002 - AV-101-003

Aerovate Therapeutics Inc.0 个研究点目标入组 462 人开始时间: 2024年2月10日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
462

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
18 至 65+(—)
性别
All

入选标准

  • Consented to participate in the LTE and has successfully completed the placebo-controlled 24-week Study AV-101-002., Female subjects of childbearing potential who have agreed to continue to use a highly effective form of contraception during the LTE and for at least 30 days after completing or discontinuing study treatment.

排除标准

  • The Investigator believes that it would not be in the best interest of the subject to be included in the LTE e.g., for clinical or social reasons., Subjects who were not compliant with study medication in AV-101-002 as assessed by the Investigator.

研究者

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