APPROVED_FOR_MARKETINGNCT02189720
Expanded Access Study Amifampridine Phosphate in Lambert-Eaton Myasthenic Syndrome (LEMS),Congenital Myasthenic Syndrome
Studying Congenital myasthenic syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Catalyst Pharmaceuticals, Inc.
- Principal Investigator
- Perry Shieh, MD, PhDUniversity of California, Los Angeles
- Intervention
- Amifampridine Phosphate(drug)
- Eligibility
- 2 years · All sexes
Study locations (1)
- UCLA, Los Angeles, California, United States
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 NCT02189720 on ClinicalTrials.govOther trials for Congenital myasthenic syndrome
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