drugset / Trial / NCT04110886

Safety, Tolerability, and Pharmacokinetics of HSK21542 in Healthy Volunteers

NCT04110886

Phase 1 Completed 120 enrolled Sichuan Haisco Pharmaceutical Group Co., Ltd
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single-Ascending-Dose Study To Investigate the Safety, Tolerability, and Pharmacokinetics of a kappa receptor agonist HSK21542 in Healthy Volunteers. The study will enroll approximately 50 adults. The anticipated study duration will be up to 6 months.

Timeline

Start
2020-07-02
Primary completion
2020-12-08
Completion
2021-01-05

Drugs

EvaluationDrugModalityDoseRoute
Subject HSK21542 Peptide 0.2 ug Other
Subject HSK21542 Peptide 20 ug Other

Indications