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临床试验/CTIS2023-505919-21-00
CTIS2023-505919-21-00招募中1 期

A Phase 2A, Double-blind, Randomized, Placebo-controlled, Multi-center Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986435/MYK-224 in Participants with Heart Failure with Preserved Ejection Fraction (HFpEF) - CV029-1001

Bristol-Myers Squibb Services Unlimited Company0 个研究点目标入组 55 人开始时间: 2023年11月30日最近更新:

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
55

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

  • Adult patients with stable, symptomatic HFpEF with a normal heart pumping ability.

排除标准

  • Some key exclusion criteria include: patients must not have a known diagnosis of obstructive or genetic hypertrophic cardiomyopathy or infiltrative/storage disorder such as cardiac amyloidosis, or any other acute or serious condition that could interfere with assessments during the study or may pose a risk to the participant.

研究者

发起方
Bristol-Myers Squibb Services Unlimited Company

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