WHO ICTRP trial

A PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CLENBUTEROL IN…

EUCTR2017-005103-27-IT · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2017-005103-27-IT
Public title A PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CLENBUTEROL IN PATIENTS WITH SPINAL AND BULBAR MUSCULAR ATROPHY (SBMA)
Scientific title A PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CLENBUTEROL IN PATIENTS WITH SPINAL AND BULBAR MUSCULAR ATROPHY (SBMA) - BETA SBMA
Primary sponsor AZIENDA OSPEDALIERA DI PADOVA
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries Italy
Conditions Motor neuron disease characterized by atrophy and muscle weakness in the spinal and bulbar region MedDRA version: 20.1 Level: PT Classification code 10068597 Term: Bulbospinal muscular atrophy congenital System Organ Class: 10010331…
Interventions Trade Name: MONORES 20 mcg 30 compresse Product Name: MONORES 20 mcg 30 compresse Product Code: [024217034] Pharmaceutical Form: Tablet INN or Proposed INN: CLENBUTEROLO Current Sponsor code: nessuno Concentration unit: µg microgram(s)…
Registration date Oct 23, 2020
Target size 90
Secondary IDs BETASBMA
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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