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Clinical Trial Summary

This study is a multi-center, randomized, double-blind, placebo-controlled study. About 90 liver disease subjects with moderate or above pruritus are planned to be enrolled. They will be randomized to two dose groups (0.3 μg/kg and 0.6 μg/kg) and a placebo control group at a 1:1:1 ratio, with about 30 subjects in each group.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04999787
Study type Interventional
Source Haisco Pharmaceutical Group Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date September 16, 2021
Completion date August 3, 2022

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