Study to Evaluate IMG-004 in Healthy Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

August 8, 2022

Primary Completion Date

May 2, 2024

Study Completion Date

May 2, 2024

Conditions
Healthy Participants
Interventions
DRUG

SAD IMG-004 30mg

Each participant will be randomized to receive a single oral dose of 30mg IMG-004

DRUG

SAD IMG-004 100mg

Each participant will be randomized to receive a single oral dose of 100mg IMG-004

DRUG

SAD IMG-004 200mg

Each participant will be randomized to receive a single oral dose of 200mg IMG-004

DRUG

SAD IMG-004 400mg

Each participant will be randomized to receive a single oral dose of 400mg IMG-004

DRUG

SAD IMG-004 600mg

Each participant will be randomized to receive a single oral dose of 600mg IMG-004

DRUG

SAD Placebo 30mg

Each participant will be randomized to receive a single oral dose of 30mg matching placebo

DRUG

SAD Placebo 100mg

Each participant will be randomized to receive a single oral dose of 100mg matching placebo

DRUG

SAD Placebo 200mg

Each participant will be randomized to receive a single oral dose of 200mg matching placebo

DRUG

SAD Placebo 400mg

Each participant will be randomized to receive a single oral dose of 400mg matching placebo

DRUG

SAD Placebo 600mg

Each participant will be randomized to receive a single oral dose of 600mg matching placebo

DRUG

MAD IMG-004 50mg

Each participant will be randomized to receive daily oral dose of 50mg IMG-004 for 10 days

DRUG

MAD Placebo 50mg

Each participant will be randomized to receive daily oral dose of 50mg matching placebo for 10 days

DRUG

MAD IMG-004 150mg

Each participant will be randomized to receive daily oral dose of 150mg IMG-004 for 10 days

DRUG

MAD Placebo 150mg

Each participant will be randomized to receive daily oral dose of 150mg matching placebo for 10 days

DRUG

MAD IMG-004 300mg

Each participant will be randomized to receive daily oral dose of 300mg IMG-004 for 10 days

DRUG

MAD Placebo 300mg

Each participant will be randomized to receive daily oral dose of 300mg matching placebo for 10 days

DRUG

FE IMG-004 150mg

A single dose of IMG-004 at 150 mg dose level will be administered to the participants in fed and fasted states

Trial Locations (1)

32117-5116

Labcorp Cru, Daytona Beach

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Inmagene LLC

INDUSTRY

NCT05349097 - Study to Evaluate IMG-004 in Healthy Participants | Biotech Hunter | Biotech Hunter