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A Study to Evaluate Zilebesiran in Japanese Patients With Mild to Moderate Hypertension

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Contents

clinicaltrials.gov/study/NCT06423352
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT064233520
Trial Recruitment Size
360
Trial Sponsor
Alnylam Pharmaceuticals
Alnylam Pharmaceuticals
0
Clinical Trial Start Date
June 7, 2024
0
Primary Completion Date
September 30, 2025
0
Study Completion Date
September 30, 2025
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Drug0
Interventional Trial Phase
Phase 10
Phase 20
Official Name
A Phase 1/2, Randomized, Double-blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacodynamics, and Pharmacokinetics of Zilebesiran in Japanese Patients With Mild to Moderate Hypertension0
Last Updated
May 21, 2024
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Triple0
Masked Party
Investigator0
Care Provider0
Participant0

Other attributes

Intervention Treatment
Placebo0
Zilebesiran0
Study summary

The purpose of this study is to evaluate the safety, tolerability, efficacy, pharmacodynamics (PD) and pharmacokinetics (PK) of zilebesiran in Japanese patients with mild to moderate hypertension.

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