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A Study of LP-168 in Healthy Volunteers

Multiple Sclerosis Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LP-168 Following Single and Multiple Oral Administration to Healthy Volunteers

Clinical Trial Summary

This is a Phase I study designed to assess the safety, tolerability and pharmacokinetics of LP-168 in healthy human volunteers.

Clinical Trial Description

This study will enroll 70 healthy subjects, will set 4 SAD and 3 MAD dose cohorts, with 10 subjects in each dose cohort. Subjects will be assigned to L-168 or placebo group by ratio of 8:2 in each cohort. Sentinel subjects will be used in each dose cohort during the single dose phase. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05432713
Study type Interventional
Source Guangzhou Lupeng Pharmaceutical Company LTD.
Contact
Status Completed
Phase Phase 1
Start date May 14, 2022
Completion date December 28, 2022
View Details
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