Safety and Efficacy of ALXN1720 in Adults With Generalized Myasthenia Gravis
Phase 3
Active, not recruiting
- Conditions
- Generalized Myasthenia Gravis
- Registration Number
- NCT05556096
- Lead Sponsor
- Alexion Pharmaceuticals, Inc.
- Brief Summary
The purpose of this study is to evaluate the safety and efficacy of ALXN1720 for the treatment of generalized MG (gMG) in adults with autoantibodies against acetylcholine receptor (AChR).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 260
Inclusion Criteria
- Diagnosis of MG with generalized muscle weakness meeting the clinical criteria defined by Myasthenia Gravis Foundation of America (MGFA) Class II, III or IV
- Positive serological test for autoantibodies against AChR
Exclusion Criteria
- History of thymectomy, or any other thymic surgery within 12 months prior to Screening
- Untreated thymic malignancy, carcinoma, or thymoma
- History of Neisseria meningitidis infection
- Pregnancy, breastfeeding, or intention to conceive during the course of the study
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change From Baseline in Myasthenia Gravis-Activities of Daily Living (MG-ADL) Total Score at Week 26 Baseline, Week 26
- Secondary Outcome Measures
Name Time Method Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 26 Baseline, Week 26 Percentage of Responders Based on Reduction of the MG-ADL Total Score at Week 26 Baseline up to Week 26 Response is defined as reduction of the MG-ADL total score by \>= 3 points from baseline at Week 26.
Percentage of Responders based on Reduction of the QMG Total Score at Week 26 Baseline up to Week 26 Response is defined as reduction of the QMG total score by \>= 5 points from baseline at Week 26
Change From Baseline in Myasthenia Gravis Composite (MGC) Total Score at Week 26 Baseline, Week 26 Change from Baseline in the QMG total score at Week 4 Baseline, Week 4
Trial Locations
- Locations (1)
Research Site
🇬🇧Sheffield, United Kingdom
Research Site🇬🇧Sheffield, United Kingdom