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Clinical Trial Summary

The purpose of this study is to evaluate the safety, effectiveness and pharmacokinetics of a study drug called Faslodex (fulvestrant) in the treatment of progressive precocious puberty (PPP) (early puberty) in girls with McCune-Albright syndrome (MAS)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00278915
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 2
Start date January 31, 2006
Completion date July 20, 2023

See also
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Active, not recruiting NCT03628937 - The Effect of Decaffeinated Green Tea Polyphenol Intake on the Risk of Precocious Puberty Among Obese Girls N/A
Enrolling by invitation NCT02790112 - Long-term Outcome of GnRH Analogues Treatment of Children With Idiopathic Central Precocious Puberty N/A