Drug class
Somatostatic Agents
Somatostatic agents, more commonly recognized in clinical and pharmacological reference compendia as somatostatin analogs, are a therapeutic class of synthetic peptide compounds designed to mimic the inhibitory actions of endogenous somatostatin. Read more about Somatostatic Agents
25 drugs in this class 21 manufacturers
Drugs in Somatostatic Agents
OCTREOTIDE ACETATE
MYCAPSSA (octreotide acetate)
OCTREOTIDE ACETATE ER (octreotide acetate, microspheres)
SANDOSTATIN (octreotide acetate)
SANDOSTATIN LAR DEPOT (octreotide acetate, microspheres)
LANREOTIDE ACETATE
Somatostatic agents, more commonly recognized in clinical and pharmacological reference compendia as somatostatin analogs, are a therapeutic class of synthetic peptide compounds designed to mimic the inhibitory actions of endogenous somatostatin.
These agents exert their principal therapeutic effects by binding with high affinity to somatostatin receptors (predominantly SSTR2 and SSTR5), thereby suppressing the hypersecretion of endocrine and paracrine hormones—such as growth hormone, insulin-like growth factor 1, glucagon, and serotonin—while also providing antiproliferative tumor control and reducing splanchnic blood flow.
Clinically, members of this class (including octreotide, lanreotide, and pasireotide) are primarily utilized in the management of acromegaly, symptomatic gastroenteropancreatic neuroendocrine tumors (such as carcinoid syndrome), Cushing disease, and acute bleeding from gastroesophageal varices.
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cetaf.org
Somatostatic agents, more commonly recognized in clinical and pharmacological reference compendia as somatostatin analogs, are a therapeutic class of synthetic peptide compounds designed to mimic the inhibitory actions of endogenous somatostatin
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connectrx.com
Somatostatic agents, more commonly recognized in clinical and pharmacological reference compendia as somatostatin analogs, are a therapeutic class of synthetic peptide compounds designed to mimic the inhibitory actions of endogenous somatostatin
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molinahealthcare.com
These agents exert their principal therapeutic effects by binding with high affinity to somatostatin receptors (predominantly SSTR2 and SSTR5), thereby suppressing the hypersecretion of endocrine and paracrine hormones—such as growth hormone, insulin-like growth factor 1, glucagon, and serotonin—while also providing antiproliferative tumor control and reducing splanchnic blood flow Clinically, members of this class (including octreotide, lanreotide, and pasireotide) are primarily utilized in the...
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mainecarepdl.org
These agents exert their principal therapeutic effects by binding with high affinity to somatostatin receptors (predominantly SSTR2 and SSTR5), thereby suppressing the hypersecretion of endocrine and paracrine hormones—such as growth hormone, insulin-like growth factor 1, glucagon, and serotonin—while also providing antiproliferative tumor control and reducing splanchnic blood flow
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karger.com
These agents exert their principal therapeutic effects by binding with high affinity to somatostatin receptors (predominantly SSTR2 and SSTR5), thereby suppressing the hypersecretion of endocrine and paracrine hormones—such as growth hormone, insulin-like growth factor 1, glucagon, and serotonin—while also providing antiproliferative tumor control and reducing splanchnic blood flow
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wa.gov
Clinically, members of this class (including octreotide, lanreotide, and pasireotide) are primarily utilized in the management of acromegaly, symptomatic gastroenteropancreatic neuroendocrine tumors (such as carcinoid syndrome), Cushing disease, and acute bleeding from gastroesophageal varices
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aetna.com
Clinically, members of this class (including octreotide, lanreotide, and pasireotide) are primarily utilized in the management of acromegaly, symptomatic gastroenteropancreatic neuroendocrine tumors (such as carcinoid syndrome), Cushing disease, and acute bleeding from gastroesophageal varices
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