Clinical Trials Directory

Trials / Completed

CompletedNCT05140863

To Evaluate the Efficacy and Safety of HSK16149 Capsule in Chinese Patients With Postherpetic Neuralgia

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, 12-Week, Phase 3 Study to Evaluate the Efficacy and Safety of HSK16149 Capsules in Chinese Patients With Postherpetic Neuralgia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
372 (actual)
Sponsor
Haisco Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Investigate the Efficacy and Safety of HSK16149 capsules in Chinese Postherpetic Neuralgia Following 12 Weeks Treatment in Comparison to Placebo

Conditions

Interventions

TypeNameDescription
DRUGHSK16149 20mg BIDHSK16149 20mg, orally twice a day, treatment period; 12-weeks fixed dose
DRUGHSK16149 40mg BIDHSK16149 40mg, orally twice a day, treatment period; 12-weeks fixed dose
DRUGPlacebo BIDPlacebo, orally twice a day, treatment period; 12-weeks fixed dose

Timeline

Start date
2021-11-01
Primary completion
2022-12-22
Completion
2023-01-05
First posted
2021-12-02
Last updated
2023-02-27

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05140863. Inclusion in this directory is not an endorsement.

To Evaluate the Efficacy and Safety of HSK16149 Capsule in Chinese Patients With Postherpetic Neuralgia (NCT05140863) · Clinical Trials Directory