CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 31 enrolled
Drug / intervention
Zilucoplandrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06471361
NCT06471361Phase 3Completed

A Multicenter, Open-Label, Outpatient Study to Evaluate the Safe And Effective Use of a Zilucoplan Auto-Injector Combination Product for Subcutaneous Self-Administration by Study Participants With Generalized Myasthenia Gravis

UCB Biopharma SRL·interventional·Posted Jun 24, 2024·Updated Mar 27, 2026

In Brief

A Phase 3 clinical trial evaluating Zilucoplan for Generalized Myasthenia Gravis. Completed, enrolled 31 participants across 11 sites in 3 countries.

Detailed Summary

The purpose of this study is to evaluate the effectiveness, safety and tolerability of zilucoplan auto-injector (ZLP-AI) self-administration.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPoland, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20252026
First PostedJun 24, 2024
Enrollment StartAug 27, 2024
Primary CompletionJan 28, 2025
Study CompletionFeb 3, 2025
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 2.0 years ago

Interventions

Zilucoplandrug

Zilucoplan will be self-administered subcutaneously by study participants at pre-specified time points.