RecruitingNCT06078553

A Natural History Study in Participants With Congenital Myasthenic Syndromes (CMS) Due to Mutations in DOK7, MUSK, AGRN, or LRP4

Studying Congenital myasthenic syndrome

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Key facts

Sponsor
argenx
Enrollment
100 enrolled
Eligibility
2 years · All sexes
Timeline
20242027

Study locations (19)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06078553 on ClinicalTrials.gov

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