A SAD Study to Evaluate the Safety, Tolerability and PK/PD of iN1011-N17 in Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

104

Participants

Timeline

Start Date

September 30, 2020

Primary Completion Date

October 8, 2023

Study Completion Date

October 8, 2023

Conditions
OsteoarthritisPainPost Herpetic NeuralgiaNeuropathic PainChronic PainNav 1.7
Interventions
DRUG

iN1011-N17

"This study will be conducted in approximately 104 healthy subjects in up to 13 sequential dose cohorts. Thirteen cohorts will consist of up to 8 subjects, including 2 subjects receiving placebo and 6 subjects receiving iN1011-N17.~Each subsequent cohort will continue to be randomized and dosed until maximum exposure is attained or a stopping criterion has been reached."

DRUG

Placebo

Matching Placebo for each formulations

Trial Locations (1)

3004

Nucleus Network, Melbourne

All Listed Sponsors
lead

iN Therapeutics Co., Ltd.

INDUSTRY

NCT05496205 - A SAD Study to Evaluate the Safety, Tolerability and PK/PD of iN1011-N17 in Healthy Volunteers | Biotech Hunter | Biotech Hunter