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

  • STATUS
    Not Recruiting
  • participants needed
    92
  • sponsor
    Guangdong Hengrui Pharmaceutical Co., Ltd
Updated on 27 November 2022
Accepts healthy volunteers

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.

Details
Condition Chronic Cough
Treatment HRS-2261 tablet、placebo
Clinical Study IdentifierNCT05274516
SponsorGuangdong Hengrui Pharmaceutical Co., Ltd
Last Modified on27 November 2022

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