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Clinical Trial Summary

The study will investigate the efficacy, safety and pharmacokinetics of triptorelin 22.5 mg 6-month formulation in 44 patients suffering from central precocious puberty. The total study duration per patient will be 12 months (48 weeks).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01467882
Study type Interventional
Source Debiopharm International SA
Contact
Status Completed
Phase Phase 3
Start date April 2012
Completion date July 2014

See also
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