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A Trial of HRS-2261 in Healthy Subjects After Single and Multiple Oral Administration

Chronic Cough Clinical Trial

Official title:
Phase I Clinical Study on the Safety, Tolerability, and Pharmacokinetics of HRS-2261, the Effects of Food on the Pharmacokinetics of HRS-2261, and the Effects of HRS-2261 on CYP3A4 Metabolic Enzymes in Healthy Subjects After Single and Multiple Oral Administration

Clinical Trial Summary

This is a first-in-human study that will investigate the safety, tolerability and pharmacokinetics of single and multiple ascending doses of HRS-2261 using a double blind, placebo controlled, randomized study design. The influence of food on the pharmacokinetics of HRS-2261 and the effects of HRS-2261 on CYP3A4 metabolic enzymes will also be investigated.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05274516
Study type Interventional
Source Guangdong Hengrui Pharmaceutical Co., Ltd
Contact
Status Completed
Phase Phase 1
Start date March 28, 2022
Completion date October 25, 2022
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