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Trials / Completed

CompletedNCT05642585

A Study of Single-dose MY008211A in Healthy Adults

A Phase I, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Doses Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic/Pharmacodynamics Characteristics of MY008211A Tablets in Healthy Adult Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Wuhan Createrna Science and Technology Co., Ltd · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The trial is the first human trial. The safety, tolerability, PK and PD of MY008211A Tablets will be evaluated in healthy subjects.

Detailed description

This is a single ascending dose, randomized, double-blind study,with 5 dose groups preset.

Conditions

Interventions

TypeNameDescription
DRUGMY008211A tabletsSingle oral
DRUGPlaceboSingle oral

Timeline

Start date
2022-05-27
Primary completion
2023-06-04
Completion
2023-06-04
First posted
2022-12-08
Last updated
2023-09-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05642585. Inclusion in this directory is not an endorsement.

A Study of Single-dose MY008211A in Healthy Adults (NCT05642585) · Clinical Trials Directory