SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesOtherOctreotide

Octreotide

/ Synthetic cyclic octapeptide analog of somatostatin; SSTR2/SSTR5 agonist
TIER 1 · ClinicalN = 0 · TESTING PENDINGLAST REVIEW 2026·04·20

ALIAS · Sandostatin · Sandostatin LAR

Pass rate
0
Samples
0
Suppliers
Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

Terms in this page you can click for a plain-English popup: , , , , , , , .

§ A · Identity
Primary sequence— sequence not captured —
MW · CLASS · Synthetic cyclic octapeptide analog of somatostatin; SSTR2/SSTR5 agonistCATEGORY · Other

FDA-approved (Sandostatin, 1988) for acromegaly, carcinoid syndrome, and VIPoma. Long-acting release (LAR) formulation provides once-monthly dosing.

§ B · Mechanism of action

Octreotide is a synthetic cyclic octapeptide analog of somatostatin with preferential affinity for SSTR2 and SSTR5 receptors. It inhibits GH release (used in acromegaly), serotonin and vasoactive intestinal peptide secretion (used in carcinoid syndrome and VIPoma), and has broader effects on gastrointestinal hormone secretion.

§ C · Human clinical evidence

Extensive clinical history since 1988 approval. Standard of care for medical therapy of acromegaly, symptomatic management of carcinoid syndrome, and hormone-secreting neuroendocrine tumors.

§ F · Safety signal

Common: gastrointestinal AEs (diarrhea, abdominal pain, steatorrhea), gallstone formation with chronic use (10-20% over years), glucose intolerance or hypoglycemia. Bradycardia at higher doses.

§ H · Regulatory status

Regulatory status

FDA status:
FDA-approved
Compounding:
Not eligible for compounding (approved, not in shortage)