Overview

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of mRNA-6231 in Healthy Adults

Status:
Recruiting
Trial end date:
2022-11-15
Target enrollment:
0
Participant gender:
All
Summary
The main goal of this study is to evaluate the safety and tolerability of escalating doses of a single subcutaneous (SC) administration of mRNA-6231.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
ModernaTX, Inc.
Criteria
Key Inclusion Criteria:

- Understand and agree to comply with the study procedures and provide written informed
consent

Key Exclusion Criteria:

- Has received any investigational product (for example, study drug, biologic, device)
within 30 days or 5 elimination half-lives, whichever is longer

- Pregnant or lactating women

- Men and women of childbearing potential without effective contraception during the
study

- Has any lab abnormalities or clinically significant medical condition that could
interfere with the interpretation of study results or limit the participant's
enrollment