Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT06220669

A Study of LY3541860 in Adult Participants With Relapsing Multiple Sclerosis

An Adaptive Phase 2a/2b, Randomized, Double-Blind, Parallel-Group Study to Investigate the Safety and Efficacy of LY3541860 Compared to Placebo in Slowing the Occurrence of New T1 Gadolinium-Enhancing Lesions in Adult Participants With Relapsing Multiple Sclerosis

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

The main purpose of this study is to evaluate the safety and efficacy of LY3541860 in adult participants with multiple sclerosis that gets worse and gets better. The study will last about 9 months with additional 6 months follow-up.

Conditions

Interventions

TypeNameDescription
DRUGLY3541860Administered IV
DRUGPlaceboAdministered IV

Timeline

Start date
2024-03-19
Primary completion
2025-10-18
Completion
2026-07-01
First posted
2024-01-24
Last updated
2026-04-07

Locations

20 sites across 7 countries: United States, France, Italy, Latvia, Poland, Slovakia, United Kingdom

Regulatory

Source: ClinicalTrials.gov record NCT06220669. Inclusion in this directory is not an endorsement.

A Study of LY3541860 in Adult Participants With Relapsing Multiple Sclerosis (NCT06220669) · Clinical Trials Directory