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Evaluating the Safety and Effects of AMP-101 in People With DOK7 Congenital Myasthenia Syndrome

StatusNot Yet Recruiting
PhasePhase 1
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Study First Submitted
This study is evaluating the safety and potential effects of AMP-101 in people with DOK7 Congenital Myasthenia Syndrome (CMS). Participants will receive a single dose of the study treatment and will be monitored to assess their health and response to treatment. Approximately 4 participants are expected to take part in the study.
Trial Details
NCT Number NCT07830563
Lead Sponsor Amplo Biotechnology
Conditions
(from sponsor)
Congenital Myasthenia Syndrome
Related terms Myasthenic Syndromes, Congenital
Enrollment 4 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov