Treatment of Lambert-Eaton Syndrome With 3,4 Diaminopyridine

NCT00994916 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2019-07-09

No results posted yet for this study

Summary

The purpose of the study is to provide expanded access (compassionate use) of 3,4 diaminopyridine to patients with Lambert-Eaton myasthenic syndrome (LEMS).

Conditions

  • Lambert-Eaton Myasthenic Syndrome

Interventions

DRUG

3,4 diaminopyridine

3,4 diaminopyridine up to 80 mg daily in divided doses

Sponsors & Collaborators

  • Jacobus Pharmaceutical

    collaborator INDUSTRY
  • David Lacomis, MD

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00994916 on ClinicalTrials.gov