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A Placebo-controlled Study to Evaluate the Efficacy and Safety of Clenbuterol in Patients With Spinal and Bulbar Muscular Atrophy (SBMA)
There is no cure to arrest or delay SBMA progression. It is estimated that \~1000 individuals are affected by SBMA in Italy at any given time (prevalence: 1.5/100000) with an annual incidence of 0.19/100000 males. Here, we are going to test the potential of beta2-agonist stimulation on muscle as a therapeutic avenue for SBMA. We have provided pre-clinical evidence that β-agonist stimulation may be a therapeutic strategy for SBMA. Moreover, we have shown that beta2-agonists are effective in improving motor function without relevant adverse events in a small cohort of SBMA patients. To establish safety and efficacy of clenbuterol as a cure for SBMA, we are conducting a multicenter, phase II, randomized, double-blind, parallel-group, single dose, placebo-controlled trial. Indeed, based on our preliminary data, some concerns remain to be addressed.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Azienda Ospedale Università di Padova
Padua, PD, Italy
Start Date
April 13, 2024
Primary Completion Date
June 30, 2027
Completion Date
December 31, 2027
Last Updated
April 15, 2024
90
ESTIMATED participants
Clenbuterol
DRUG
Placebo
DRUG
Lead Sponsor
Gianni Soraru
Collaborators
NCT04944940
NCT03555578
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT02024932