The purpose of this study was to gain more insight into the mechanism of action of pasireotide in patients who completed the PAOLA study. PAOLA was a 24-week, Phase III, randomized, three-arm study of pasireotide LAR 40 and 60 mg versus octreotide LAR 30 mg or lanreotide Autogel 120 mg in patients with inadequately controlled acromegaly. The current work was a planned exploratory objective of the PAOLA study that evaluated changes in levels of growth hormone (GH), insulin-like growth factor 1 (IGF-1), IGF-binding proteins (IGFBP-2, IGFBP-3), glycated haemoglobin (HbA1c) and fasting plasma glucose (FPG) in each treatment arm. Responders to pasireotide LAR (mean GH levels <2.5 μg/L and normal IGF-1 levels at 24 weeks) had lower GH and IGF-1 l...
Background: Pasireotide is a novel somatostatin analogue with higher affinity to 4/5 known human som...
Aim: To assess the efficacy and safety of pasireotide long-Acting release (PAS-LAR) alone or in comb...
International audienceObjective In the Phase III PAOLA study (clinicaltrials.gov: NCT01137682), enro...
The purpose of this study was to gain more insight into the mechanism of action of pasireotide in pa...
Purpose A large, randomized, double-blind, Phase III core study demonstrated that pasireotide LAR wa...
Objective: Hyperglycemia was noted in pasireotide long-acting release (PAS LAR}-treated patients wit...
International audiencePasireotide, a multireceptor-targeted somatostatin analog with highest affinit...
Pasireotide (SOM230), a multireceptor-targeted somatostatin analogue, has exhibited favorable safety...
IF 4.101International audienceThe anti-somatostatin agents used to treat acromegaly, Cushing's disea...
Background Many patients with acromegaly do not achieve biochemical control despite receiving high d...
Pasireotide has a broader somatostatin receptor binding profile than other somatostatin analogues. A...
BACKGROUND: Many patients with acromegaly do not achieve biochemical control despite receiving high...
Background: Pasireotide is a novel somatostatin analogue with higher affinity to 4/5 known human som...
Aim: To assess the efficacy and safety of pasireotide long-Acting release (PAS-LAR) alone or in comb...
International audienceObjective In the Phase III PAOLA study (clinicaltrials.gov: NCT01137682), enro...
The purpose of this study was to gain more insight into the mechanism of action of pasireotide in pa...
Purpose A large, randomized, double-blind, Phase III core study demonstrated that pasireotide LAR wa...
Objective: Hyperglycemia was noted in pasireotide long-acting release (PAS LAR}-treated patients wit...
International audiencePasireotide, a multireceptor-targeted somatostatin analog with highest affinit...
Pasireotide (SOM230), a multireceptor-targeted somatostatin analogue, has exhibited favorable safety...
IF 4.101International audienceThe anti-somatostatin agents used to treat acromegaly, Cushing's disea...
Background Many patients with acromegaly do not achieve biochemical control despite receiving high d...
Pasireotide has a broader somatostatin receptor binding profile than other somatostatin analogues. A...
BACKGROUND: Many patients with acromegaly do not achieve biochemical control despite receiving high...
Background: Pasireotide is a novel somatostatin analogue with higher affinity to 4/5 known human som...
Aim: To assess the efficacy and safety of pasireotide long-Acting release (PAS-LAR) alone or in comb...
International audienceObjective In the Phase III PAOLA study (clinicaltrials.gov: NCT01137682), enro...