Assessment of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ATH-063 in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

76

Participants

Timeline

Start Date

April 6, 2023

Primary Completion Date

February 8, 2024

Study Completion Date

February 8, 2024

Conditions
Inflammatory Bowel DiseasesCrohn DiseaseUlcerative ColitisAutoimmune Diseases
Interventions
DRUG

ATH-063

12.5 and 50 mg Capsules, anticipated dose range to be from 25 to 250 mg.

DRUG

Placebo

Identical capsule to the drug without the active ingredient.

Trial Locations (1)

5000

CMAX Clinical Research, Adelaide

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Syneos Health

OTHER

collaborator

Athos Therapeutics Australia Pty Ltd

UNKNOWN

lead

Athos Therapeutics Inc

INDUSTRY