Trial Details

Not Recruiting
Basic Information
Clinical ID c5449
Identifier ACTRN12620000910909
Trial Title A Phase I, Randomized, Double-blind, Placebo Controlled Trial to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Single- and Multiple-Ascending Doses of RS1805 Tablets in Healthy Adult Subjects
Trial URL Visit Original Page
Study Information
Study Results

Yes

Conditions Inflammatory Bowel Disease; Inflammatory Bowel Disease;Oral and Gastrointestinal - Inflammatory bowel disease
Interventions Part 1 (Single Ascending Dose)Lowest starting dose of 50 mg RS1805 tablets, and the dose level will be gradually escalated. The maximum dose in the single ascending-dose part is planned to be 600 mg RS1805 tablets administered orally. The intervention
Participant Information
Sponsor Atridia Pty Ltd
City NULL
Country/Region Australia;China
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT
Study Design
Study Type Interventional
Phase PHASE1
Time Information
Start Date NULL
Primary Completion Date NULL
Completion Date NULL