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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
NameTimeMethod
Change From Baseline in Myasthenia Gravis-Activities of Daily Living (MG-ADL) Total Score at Week 26Baseline, Week 26
Secondary Outcome Measures
NameTimeMethod
Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 26Baseline, Week 26
Percentage of Responders Based on Reduction of the MG-ADL Total Score at Week 26Baseline 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 26Baseline 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 26Baseline, Week 26
Change from Baseline in the QMG total score at Week 4Baseline, Week 4

Trial Locations

Locations (1)

Research Site

🇬🇧

Sheffield, United Kingdom

Research Site
🇬🇧Sheffield, United Kingdom

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