A Multicenter, Randomized, Double-blind, Parallel Group Study to Assess the Safety and Tolerability of Initiating LCZ696 in Heart Failure Patients Comparing Two Titration Regimens
收藏DataCite Commons2025-12-16 更新2026-05-07 收录
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https://search.vivli.org/doiLanding/studies/PR00012259/isLanding
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资源简介：
The purpose of this study is to assess the safety and tolerability of initiating LCZ696 in heart failure patients with reduced ejection fraction (HF-rEF) using conservative (reaching target dose over 6 weeks) and condensed (reaching target dose over 3 weeks) up-titration regimens.
提供机构：
Vivli
创建时间：
2025-12-16
