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An Open-label Study to Evaluate the Safety, Tolerability, and Efficacy of Subcutaneous Zilucoplan in Participants With Generalized Myasthenia Gravis Who Were Previously Receiving Intravenous Complement Component 5 Inhibitors

Completed · Phase 3 · NCT05514873

Conditions: Generalized Myasthenia Gravis

At a glance

Research payments reported, 2025
$205,833
U.S. investigators named
11
Sites paid
11
Planned or actual enrollment
26

About the trial

Sponsor
UCB Biopharma SRL
Tested
zilucoplan (RA101495) (drug)
Dates
Started 2022-10-31; completion 2024-10-23
Results posted
Yes

The purpose of the study is to evaluate the safety and tolerability of switching from intravenous (IV) complement component 5 (C5) inhibitors to subcutaneous (SC) Zilucoplan in study participants with generalized myasthenia gravis (gMG)

From ClinicalTrials.gov, last updated 2025-09-03. Full record, eligibility and contacts (opens in a new tab)

Industry funding

UCB SA reported $205,833 in research payments for this study in 2025 (11 payments).

Products named: Zilbrysq

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.