Overview

A Single-dose Escalation Safety and PK Study for PLC in Healthy Chinese

Status:
Completed
Trial end date:
2016-01-01
Target enrollment:
Participant gender:
Summary
The main objective is to evaluate the effect of single dose Propionyl-L-Carnitine Hydrochloride on clinical pharmacokinetic characteristics and its effect of clinical pharmacokinetic characteristics and safety on healthy Chinese subjects to provide a basis for market authorization registration.
Phase:
Phase 1
Details
Lead Sponsor:
Lee's Pharmaceutical Limited