Study of efficacy and safety of pasireotide LAR in patients with inadequately controlled acromegaly

Mise à jour : Il y a 4 ans
Référence : EUCTR2014-002630-31

Femme et Homme

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Extrait

Primary objective: - To evaluate the efficacy of pasireotide LAR in patients with acromegaly who are inadequately controlled with maximal approved doses of currently available somatostatin analogues Supporting Analysis for Primary objective: - To assess the proportion of patients achieving GH <1µg/L and IGF-1 <ULN by GH level.


Critère d'inclusion

  • Acromegaly