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NCT00872950: LEMS

3,4-Diaminopyridine Use in Lambert-Eaton Myasthenic Syndrome(LEMS) and Congenital Myasthenic Syndromes (CMS)

APPROVED FOR MARKETING Last updated 11 April 2022
What this trial tests

trial testing 3,4-DIAMINOPYRIDINE in Lambert-Eaton Myasthenic Syndrome. Approved for marketing.

Quick facts

Lead sponsorLahey Clinic
StatusAPPROVED FOR MARKETING
Study typeEXPANDED_ACCESS
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Lahey Clinic

Who can join

18 and older, any sex, with Lambert-Eaton Myasthenic Syndrome or Congenital Myasthenic Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine the effectiveness and adverse effects of 3,4-diaminopyridine for the treatment of the Lambert-Eaton Myasthenic Syndrome (LEMS) and Congenital Myasthenic Syndromes (CMS).

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Treating pediatric neuromuscular disorders: The future is now.
    Dowling JJ, D Gonorazky H, Cohn RD, Campbell C. · · 2018 · cited 83× · PMID 28889642 · DOI 10.1002/ajmg.a.38418
  2. The Importance of Early Treatment of Inherited Neuromuscular Conditions.
    Mackels L, Servais L. · · 2024 · cited 6× · PMID 38306060 · DOI 10.3233/jnd-230189

Verify or expand the search:

Other recruiting trials for Lambert-Eaton Myasthenic Syndrome

Currently open trials in the same condition.

Other Lahey Clinic trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00872950.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing