Trial Details

Not Recruiting
Basic Information
Clinical ID c5420
Identifier ACTRN12624000239561
Trial Title A Single Ascending dose to assess the safety, tolerability and pharmacokinetics of TP-317 under fasted conditions in adult healthy volunteers.
Trial URL Visit Original Page
Study Information
Study Results

Yes

Conditions Inflammatory bowel disease; Inflammatory bowel disease;Oral and Gastrointestinal - Inflammatory bowel disease
Interventions The study consists of 3 planned dose cohorts where each cohort will enrol a total of 8 participants of which 6 randomised to TP-317 treatment arm and 2 randomised to the placebo treatment arm. A total of 24 participants will be enrolled for this study.<br
Participant Information
Sponsor Thetis Pharmaceuticals LLC
City NULL
Country/Region Australia
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type Interventional
Phase PHASE1
Time Information
Start Date NULL
Primary Completion Date NULL
Completion Date NULL