Clinical Trial

A Phase 1, First-in-human Study of MORF-440 (LY4292009) in Healthy Participants

Completed Phase 1
View on ClinicalTrials.gov →
Summary
The purpose of this study is to evaluate the safety and tolerability of single ascending doses of MORF-440 administered to healthy participants single-ascending dose (SAD) and maximum ascending dose (MAD) substudy.
Protocol Amendment History 1 change
critical Trial completed 2026-04-18
Trial Details
NCT Number NCT06977880
Lead Sponsor Morphic Therapeutic, Inc. (A Wholly Owned Subsidiary of Eli Lilly and Company)
Conditions Healthy
Enrollment 80 participants
Start Date 2025-02-19
Primary Completion 2026-03-20 (estimated)
Study Completion 2026-03-20 (estimated)
Updated on ClinicalTrials.gov 2026-04-17