NCT06764160CompletedPhase 3
Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Eculizumab in Chinese Adults With gMG
An Open-label, Single-arm, Multi-center Study to Evaluate the Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Eculizumab in Chinese Participants With Refractory Generalized Myasthenia Gravis (gMG)
Source: ClinicalTrials.gov · Last updated 15 Jan 2026
Brief summary (registry, in English)
This is an open-label, single-arm, multi-center study to evaluate the efficacy, safety, PK, PD, and immunogenicity of eculizumab in Chinese participants with refractory gMG. Approximately 15 participants will be enrolled in the study.
- Status (registry)
- Completed
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 15 (actual)
- First submitted
- 11 Dec 2024
- Start date
- 6 Jan 2025
- Primary completion date
- 29 Dec 2025
- Lead sponsor
- Alexion Pharmaceuticals, Inc.
- Diseases
- Myasthenia gravis
- NCT number
- NCT06764160
What you commit to
- Study type: Interventional · Phase 3
- Participants enrolled: 15
- From 6 Jan 2025 to the primary completion date, 29 Dec 2025
- 5 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- History of thymectomy or any other thymic surgery within 6 months prior to Screening. Participants with a history of treated thymic malignancy or carcinoma are eligible if they meet all of the following conditions:
- Treatment completed \> 5 years prior to the Screening Visit
- No recurrence within the 5 years prior to the Screening Visit
- No radiological indication of recurrence in a computed tomography (CT) or magnetic resonance imaging (MRI) scan, including administration of intravenous (IV) contrast, performed within 6 months of first dose on Day 1
Other illness
- Any untreated thymic malignancy, carcinoma, or thymoma
- History of N meningitidis infection or unresolved meningococcal disease
Other
- Weakness only affecting ocular or peri-ocular muscles (MGFA Class I)
- MG crisis at Screening (MGFA Class V). However, such participants may be rescreened with Alexion approval once they are treated and medically stable, in the opinion of the Investigator
Who the study is looking for
- Diagnosis of MG must be made by the following tests:
- Positive serologic test for anti-AChR Abs as confirmed at Screening, and
- One of the following:
- Abnormal neuromuscular transmission demonstrated by repetitive nerve stimulation, or
- History of positive anticholinesterase test, eg, neostigmine test, or
- Participant has demonstrated improvement in MG signs on oral cholinesterase inhibitors as assessed by the treating physician
- MGFA Clinical Classification Class II to IV at Screening
- MG-ADL total score must be ≥ 6 at Screening and Day 1
- Participants who have:
- Failed treatment with 2 or more ISTs over one year (either in combination or as monotherapy), ie, continue to have impairment ADLs (persistent weakness, experience crisis, or unable to tolerate IST) despite ISTs or,
- Failed at least one IST and require chronic PE or IVIg to control symptoms, ie, participants who require PE or IVIg on a regular basis for the management of muscle weakness at least 2 cycles over last 12 months
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (5)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| - Coordinator of this site? Confirm its status | Changchun | China | Unknown status |
| - Coordinator of this site? Confirm its status | Fuzhou | China | Unknown status |
| - Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
| - Coordinator of this site? Confirm its status | Qingdao | China | Unknown status |
| - Coordinator of this site? Confirm its status | Shanghai | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.