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Open-Label Extension of Zilucoplan in Subjects With Generalized Myasthenia Gravis
NCT04225871 · View on ClinicalTrials.gov ↗
Study Summary
The RAISE-XT study is an open-label extension study to evaluate the long-term efficacy, safety, and tolerability of zilucoplan in subjects with gMG who have previously participated in a qualifying Ra Pharmaceuticals sponsored zilucoplan study.
Conditions Studied
Interventions
- DRUG zilucoplan (RA101495)
Study Locations (20)
California
- Mg0011 31 — Irvine
- MG0011 4 — Los Angeles
- Mg0011 220 — Pasadena
- Mg0011 160 — San Francisco
New York
- Mg0011 30 — Buffalo
- Mg0011 123 — Great Neck
- Mg0011 23 — New York
Michigan
- Mg0011 33 — Detroit
- Mg0011 49 — East Lansing
Alabama
- Mg0011 41 — Mobile
Arizona
- Mg0011 116 — Phoenix
Connecticut
- Mg0011 24 — New Haven
District of Columbia
- Mg0011 27 — Washington D.C.
Florida
- Mg0011 25 — Tampa
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2019-12-23 |
| Est. Completion | 2026-06-02 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04225871
The ClinicalTrials.gov registry entry for NCT04225871 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Biopharma SRL, which has 116 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Generalized Myasthenia Gravis appearing as the primary indexed condition, and to 1 intervention — of which zilucoplan (RA101495) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04225871 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, New York, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04225871 about?
NCT04225871 is a clinical study titled "Open-Label Extension of Zilucoplan in Subjects With Generalized Myasthenia Gravis". The RAISE-XT study is an open-label extension study to evaluate the long-term efficacy, safety, and tolerability of zilucoplan in subjects with gMG who have previously participated in a qualifying Ra Pharmaceuticals sponsored zilucoplan study.
What is the current status of trial NCT04225871?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 200 participants. The study started on 2019-12-23. Estimated completion is 2026-06-02.
What conditions does trial NCT04225871 study?
This clinical trial studies the following conditions: Generalized Myasthenia Gravis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04225871?
The interventions under investigation include: zilucoplan (RA101495) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04225871?
This trial is sponsored by UCB Biopharma SRL, which has 116 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04225871 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Connecticut, District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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