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A Phase 3, Double-blind, Placebo-controlled, Randomized Discontinuation Study Followed by Open-label Extension Evaluating Efficacy and Safety of Amifampridine Phosphate in Patients With Lambert-Eaton Myasthenic Syndrome (LEMS)

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01377922
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:36:42.928828+00:00
Published At
2018-01-04T00:00:00+00:00
Record Updated At
2018-01-04
Results Posted At
2018-01-04
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Lambert Eaton Myasthenic Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2018-01-04"
protocolSection.identificationModule.nctId
"NCT01377922"
protocolSection.identificationModule.officialTitle
"A Phase 3, Double-blind, Placebo-controlled, Randomized Discontinuation Study Followed by Open-label Extension Evaluating Efficacy and Safety of Amifampridine Phosphate in Patients With Lambert-Eaton Myasthenic Syndrome (LEMS)"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2018-01-04"

Study condition terms

  • Lambert Eaton Myasthenic Syndrome (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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