RecruitingPhase 1NCT06436742

A Phase 1b Study to Investigate Safety and Tolerability of ARGX-119 in Adult Participants With DOK7-Congenital Myasthenic Syndromes (CMS)

Studying Congenital myasthenic syndrome

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Key facts

Sponsor
argenx
Intervention
ARGX-119(biological)
Enrollment
16 enrolled
Eligibility
18 years · All sexes
Timeline
20242028

Study locations (9)

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 NCT06436742 on ClinicalTrials.gov

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