WHO ICTRP trial

Estudio multicéntrico para comprobar la respuesta clínico-analítica de pacientes…

EUCTR2007-005808-41-ES · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2007-005808-41-ES
Public title Estudio multicéntrico para comprobar la respuesta clínico-analítica de pacientes portadores sintomáticos de Disferlinopatía al tratamiento con Calcifediol Multicentric study to assess the clinical and analytical response to calcifediol in symptomatic carriers of dysferlin myopathy
Scientific title Estudio multicéntrico para comprobar la respuesta clínico-analítica de pacientes portadores sintomáticos de Disferlinopatía al tratamiento con Calcifediol Multicentric study to assess the clinical and analytical response to calcifediol in symptomatic carriers of dysferlin myopathy
Primary sponsor Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Countries Spain
Conditions Portadores sintomaticos de una mutación en el gen disferlina. Symptomatic carriers of a mutation in the dysferlin gene MedDRA version: 9.1 Level: LLT Classification code 10028356 Term: Muscular dystrophy
Interventions Trade Name: Hidroferol® Product Name: Calcifediol Pharmaceutical Form: Oral liquid INN or Proposed INN: CALCIFEDIOL CAS Number: 19356-17-3 Other descriptive name: HIDROFEROL Concentration unit: mg milligram(s) Concentration type: equal…
Registration date Jan 25, 2008
Secondary IDs EC 07/90601
Registry page clinicaltrialsregister.eu

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