Clinical Trials Directory

Trials / Unknown

UnknownNCT01730209

Efficacy of RAD001/Everolimus in Autism and NeuroPsychological Deficits in Children With Tuberous Sclerosis Complex

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Erasmus Medical Center · Academic / Other
Sex
All
Age
4 Years – 15 Years
Healthy volunteers
Not accepted

Summary

Tuberous sclerosis complex (TSC) is a genetic disease that leads to mental retardation in over 50% of patients, and to learning problems, behavioral problems, autism and epilepsy in up to 90% of patients. The underlying deficit of TSC, loss of inhibition of the mammalian target of rapamycin (mTOR) protein due to dysfunction of the tuberin/hamartin protein complex, can be rescued by everolimus. Everolimus has been registered as treatment for renal cell carcinoma and giant cell astrocytoma (SEGA). Evidence in human and animal studies suggests that mTOR inhibitors improve learning and development in patients with TSC.

Detailed description

Randomized double-blind placebo controlled intervention study in children with TSC between age 4 and 15 years with an intelligence quotient (IQ) estimated \<80 and/or special schooling and/or autism spectrum disorder and/or learning disability requiring remedial teaching. Patients are randomised to receive everolimus or placebo during a period of 12 months.

Conditions

Interventions

TypeNameDescription
DRUGEverolimusEverolimus once daily titrated to trough levels of 5-10 ng/ml.
DRUGPlacebo

Timeline

Start date
2012-11-01
Primary completion
2015-11-01
Completion
2016-11-01
First posted
2012-11-21
Last updated
2015-05-05

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01730209. Inclusion in this directory is not an endorsement.