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Study of CD388 Subcutaneous Administration in Healthy Japanese Subjects

Healthy Clinical Trial

Official title:
A Phase 1, Randomized, Double-Blind, Single Ascending Dose Study to Determine the Safety, Tolerability, and Pharmacokinetics of CD388 Subcutaneous Administration in Healthy Japanese Subjects

Clinical Trial Summary

The purpose of this study is to determine the safety and tolerability profile of CD388 Injection, as compared to saline placebo, when dosed by subcutaneous (SQ) administration as a single dose to healthy Japanese adult subjects.

Clinical Trial Description

This is a Phase 1, single-center, prospective, randomized, double-blind study of ascending single doses of CD388 Injection administered SQ to healthy Japanese adult subjects. The goals are to assess safety, tolerability, and pharmacokinetics (PK) of CD388. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05619536
Study type Interventional
Source Cidara Therapeutics Inc.
Contact
Status Completed
Phase Phase 1
Start date October 18, 2022
Completion date July 14, 2023
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