Overview

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

Status:
Recruiting
Trial end date:
2022-08-24
Target enrollment:
Participant gender:
Summary
A First-in-Human, Double-blind, Randomized, Placebo-controlled, Single Ascending Dose Study to Evaluate Safety, Tolerability, Pharmacokinetics/Pharmacodynamics of iN1011-N17 after Oral Administration in Healthy Volunteers.
Phase:
Phase 1
Details
Lead Sponsor:
iN Therapeutics Co., Ltd.