The primary objective of this study is to evaluate the safety and efficacy of anastrozole 1 mg given once daily in subjects with McCune-Albright Syndrome.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Arimidex (anastrozole) 1mg once daily by mouth
Research Site
Montpellier, France
Research Site
Paris, France
Research Site
Berlin, Germany
Research Site
Erlangen, Germany
Research Site
The efficacy of study treatment will be assessed based on the change from baseline measurements relating to vaginal bleeding, bone age, and growth velocity
Time frame: 12 months or until the subject demonstrates the lack of efficacy bases upon progression of primary endpoints or experiences serious drug-related toxicity requiring withdrawal
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Osnabrück, Germany
Research Site
Torino, Italy
Research Site
London, United Kingdom