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Trials / Completed

CompletedNCT06519981

Phase 1 Study of HRS-9231 Safety and Pharmacokinetics in Healthy Caucasians

A Phase 1, Randomized, Double-Blind, Placebo-Controlled Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of HRS-9231 in Healthy Caucasian Participants

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Atridia Pty Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This is a phase 1, randomized, double-blind, placebo-controlled study. The objective of this study is to evaluate the safety, tolerability, and PK profile of HRS-9231 injection following a single dose in healthy Caucasian participants.

Conditions

Interventions

TypeNameDescription
DRUGHRS-9231or matching placeboHRS-9231 injection or matching placebo will be administered through IV injection.

Timeline

Start date
2024-08-21
Primary completion
2024-09-29
Completion
2024-11-27
First posted
2024-07-25
Last updated
2024-12-06

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT06519981. Inclusion in this directory is not an endorsement.

Phase 1 Study of HRS-9231 Safety and Pharmacokinetics in Healthy Caucasians (NCT06519981) · Clinical Trials Directory