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Pasireotide

Somatostatin Analog — SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS

Also known as: pasireotide diaspartate, pasireotide disapartate, pasireotide embonate, pasireotide pamoate, signifor, SOM 230, SOM230

OnpFDA approvedOrphan designationATC H01CB05

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Pasireotide is an onp drug in the Somatostatin Analog class catalogued in DrugCentral. It was first approved by the FDA in 2012. Its mechanism of action is classified as Somatostatin Receptor Agonists. DrugCentral lists 5 molecular targets, including SSTR5, Sstr2 and SSTR2. Recorded indications include Hypercortisolism.

  • Approval status: onp (first approved 2012 by the FDA).
  • Drug class: Somatostatin Analog.
  • Mechanism of action: Somatostatin Receptor Agonists.
  • Molecular targets: SSTR5, Sstr2, SSTR2 and SSTR3 (5 listed in DrugCentral).
  • Indications: Hypercortisolism.
  • ATC code: H01CB05 (Somatostatin and analogues).
  • Molecular formula: C58H66N10O9; molecular weight 1047.23 g/mol.

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (1)

  • Hypercortisolism

Mechanism & targets

Mechanism of action (MoA)Somatostatin Receptor Agonists
Established pharmacologic classSomatostatin Analog

Molecular targets (5)

TargetGeneActionActivity
Somatostatin receptor type 5SSTR5agonistIC50 9.80
Somatostatin receptor type 2Sstr2agonistEC50 9.07
Somatostatin receptor type 2SSTR2agonistIC50 9.00
Somatostatin receptor type 3SSTR3agonistIC50 8.80
Somatostatin receptor type 1SSTR1agonistIC50 8.00

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
2012-12-14FDA—NOVARTISYes

ATC classification

ATC codeTherapeutic hierarchy
H01CB05SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS › PITUITARY AND HYPOTHALAMIC HORMONES AND ANALOGUES › HYPOTHALAMIC HORMONES › Somatostatin and analogues

Reported adverse-event signals

Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.

MedDRA termLLR
Hyperglycaemia757.9
Diabetes mellitus605.4
Blood glucose increased138.1
Glycosylated haemoglobin increased124.3
Adrenal insufficiency119.3
Hypoglycaemia110.7
Cholelithiasis92.7
Diabetes mellitus inadequate control87.9
Polyuria82.2
Hyperadrenocorticism80.7
Cortisol free urine increased80.5
Insulin-like growth factor increased73.8

Chemical structure

Molecular formulaC58H66N10O9
Molecular weight1047.23 g/mol
CAS number—
InChIKeyVMZMNAABQBOLAK-SLLFKNDXSA-N
PubChem CID9941444
NCCCC[C@@H]1NC(=O)[C@@H](CC2=CNC3=C2C=CC=C3)NC(=O)C(NC(=O)[C@@H]2C[C@H](CN2C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC2=CC=C(OCC3=CC=CC=C3)C=C2)NC1=O)OC(=O)NCCN)C1=CC=CC=C1

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Pasireotide used for?

DrugCentral lists the following indications for Pasireotide: Hypercortisolism.

How does Pasireotide work?

Pasireotide is classified as Somatostatin Receptor Agonists; its molecular targets in DrugCentral include SSTR5 (agonist), Sstr2 (agonist), SSTR2 (agonist) and SSTR3 (agonist).

When was Pasireotide first approved?

Pasireotide was first approved by the FDA in 2012.

What drug class does Pasireotide belong to?

Pasireotide is in the Somatostatin Analog class.

What is the chemical formula of Pasireotide?

Pasireotide has the molecular formula C58H66N10O9 and a molecular weight of 1047.23 g/mol.

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Sources

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For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

StatusONP
First approval2012-12-14
AgencyFDA
Targets5
Indications1
FormulaC58H66N10O9
DrugCentral ID4329
Interactive profile