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Clinical Trial Summary

This study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics (PD), immunogenicity, and efficacy of subcutaneous (SC) ALXN1830 in adults with generalized myasthenia gravis (gMG).


Clinical Trial Description

Participants have the option to enroll in an Open-label Extension (OLE) Period to receive ALXN1830 up to 58 weeks (including follow-up period). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04982289
Study type Interventional
Source Alexion Pharmaceuticals
Contact
Status Withdrawn
Phase Phase 2
Start date January 1, 2022
Completion date January 31, 2024

See also
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