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Prospective, Open-label, Non-randomized, Single-arm, Multi-center Dose Titration Study to Investigate the Safety and Efficacy of NT 201 in Subjects Deemed to Require Total Body Doses of 800 U of NT 201 During the Course of the Study for the Treatment of Upper and Lower Limb Spasticity of the Same Body Side Due to Cerebral Causes

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01603459
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:36:35.945194+00:00
Published At
2017-02-03T00:00:00+00:00
Record Updated At
2017-04-26
Results Posted At
2017-02-03
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
["Spasticity of the Upper and Lower Limb Due to Cerebral Causes"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2017-04-26"
protocolSection.identificationModule.nctId
"NCT01603459"
protocolSection.identificationModule.officialTitle
"Prospective, Open-label, Non-randomized, Single-arm, Multi-center Dose Titration Study to Investigate the Safety and Efficacy of NT 201 in Subjects Deemed to Require Total Body Doses of 800 U of NT 201 During the Course of the Study for the Treatment of Upper and Lower Limb Spasticity of the Same Body Side Due to Cerebral Causes"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2017-02-03"

Study condition terms

  • Spasticity of the Upper and Lower Limb Due to Cerebral Causes (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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