Drug Detail

Information about Sandostatin

Generic Name
Octreotide acetate
IND
Octreotide
Brand Name (US)
Sandostatin
Manufacturer
Novartis
Drug Type
octapeptide mimics natural somatostatin
Delivery
Injection
Approval Status
Approved for a non-GIST application
Indications
Overall Strategy
Oncogenic Signal Path Based
Strategy
Block related tumor signal paths
Drug Category
Somatostatin receptor inhibitor

There have been a couple of papers that suggest that the somatostatin receptors are expressed in GIST and thus might be a therapeutic target.
Sandostatin® (octreotide acetate) exerts pharmacologic actions similar to the natural hormone,somatostatin. It is an even more potent inhibitor of growth hormone, glucagon, and insulin than somatostatin. Like somatostatin, it also suppresses LH response to GnRH, decreases splanchnic blood flow, and inhibits release of serotonin, gastrin, vasoactive intestinal peptide, secretin, motilin, and pancreatic polypeptide.
By virtue of these pharmacological actions, Sandostatin has been used to treat the symptoms associated with metastatic carcinoid tumors (flushing and diarrhea), and Vasoactive Intestinal Peptide (VIP) secreting adenomas (watery diarrhea).
Sandostatin substantially reduces growth hormone and/or IGF-I (somatomedin C) levels in patients with acromegaly. Single doses of Sandostatin have been shown to inhibit gallbladder contractility and to decrease bile secretion in normal volunteers. In controlled clinical trials the incidence of gallstone or biliary sludge formation was markedly increased.
Sandostatin suppresses secretion of thyroid stimulating hormone (TSH).


Links

 

Wikipedia
   

 

Somatostatin receptor expression in stromal tumors of the gastrointestinal tract
   

Trials of this drug


Trial results


Search for this drug/combination in:

ClinicalTrials.gov

ASCO

Pubmed