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Not Yet RecruitingNCT07463521

A Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Ocular Myasthenia Gravis

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Ocular Myasthenia Gravis

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
UCB Biopharma SRL · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to demonstrate the efficacy, safety and tolerability of rozanolixizumab compared with placebo in the treatment of adult study participants with Ocular Myasthenia Gravis.

Conditions

Interventions

TypeNameDescription
DRUGRozanolixizumabRozanolixizumab will be administered by subcutaneous infusion.
DRUGPlaceboPlacebo will be administered by subcutaneous infusion.

Timeline

Start date
2026-05-29
Primary completion
2028-12-01
Completion
2029-01-22
First posted
2026-03-11
Last updated
2026-03-17

Regulatory

Source: ClinicalTrials.gov record NCT07463521. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Ocular Myasthenia Gravis (NCT07463521) · Clinical Trials Directory