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Clinical Trial Summary

This is a double-blind, placebo-controlled study during which patients will receive ricolinostat or placebo.


Clinical Trial Description

This is a double-blind, placebo-controlled study during which patients will receive ricolinostat or placebo. Prior to randomization, patients will participate in the Screening and Baseline assessment period to ensure that they meet study inclusion/exclusion criteria. Following the Screening and Baseline assessment period, patients who meet entry criteria will be randomized in a 2:1 ratio to receive either ricolinostat or placebo. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05229042
Study type Interventional
Source Beijing 3E-Regenacy Pharmaceuticals Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date January 1, 2022
Completion date November 10, 2023

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