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Trials / Completed

CompletedNCT05890053

To Evaluate the Long-term Safety and Efficacy of HSK16149 in Chinese Patients With Peripheral Neuralgia

A 52-week, Open Phase III Study Evaluating the Long-term Safety and Efficacy of HSK16149 Capsules in Chinese Patients With Peripheral Neuralgia

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

Summary

Investigate the long-term(52 weeks) safety and efficacy of HSK16149 capsules in Chinese patients with periphcral neuralgia

Detailed description

Investigate the long-term(52 weeks) safety and efficacy of HSK16149 capsules in Chinese patients with Peripheral neuropathic pain

Conditions

Interventions

TypeNameDescription
DRUGHSK16149 40mg BIDHSK16149 40mg , orally twice a day, treatment period; 52-weeks fixed dose.

Timeline

Start date
2022-02-17
Primary completion
2023-07-30
Completion
2023-08-07
First posted
2023-06-06
Last updated
2025-09-04

Locations

24 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05890053. Inclusion in this directory is not an endorsement.

To Evaluate the Long-term Safety and Efficacy of HSK16149 in Chinese Patients With Peripheral Neuralgia (NCT05890053) · Clinical Trials Directory