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NOT YET RECRUITING
NCT07811089
PHASE1

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of OMS1620

Sponsor: OMass Therapeutics Australia Proprietary Ltd

View on ClinicalTrials.gov

Summary

The goal of this study is to explore the safety, drug concentrations and effects on adrenal gland hormones after a single dose or multiple doses of OMS1620 in healthy participants. In addition, the effect of food on drug concentrations will also be tested.

Official title: A Randomized, Phase 1, Double-blind, Single and Multiple-Ascending Dose and Food Effect Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of OMS1620 in Healthy Participants

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

84

Start Date

2026-09

Completion Date

2027-06

Last Updated

2026-09-09

Healthy Volunteers

Yes

Interventions

DRUG

OMS1620

OMS1620 is an oral small molecule antagonist of the melanocortin 2 receptor (MC2R), the receptor for adrenocorticotrophic hormone (ACTH)

DRUG

Placebo

matched placebo control for OMS1620