Pasireotide
Pasireotide (SOM230, trade name Signifor[2]) is an orphan drug approved in the United States[3] and Europe[4] for the treatment of Cushing's disease in patients who fail or are ineligible for surgical therapy.[5][6] It was developed by Novartis. Pasireotide is a somatostatin analog with a 40-fold increased affinity to somatostatin receptor 5 compared to other somatostatin analogs.
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Trade names | Signifor |
Other names | SOM230 |
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Routes of administration | Subcutaneous |
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ECHA InfoCard | 100.211.883 ![]() |
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Formula | C58H66N10O9 |
Molar mass | 1047.21 g/mol[1] g·mol−1 |
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Pasireotide was approved for Cushing's disease by the EMA in October 2009[7] and by the FDA in December 2012.[8]
Pasireotide LAR was approved by the FDA for treatment of acromegaly in December 2014, and had been approved for this indication by the EMA one month earlier.[9]
References
- Pasireotide | C58H66N10O9 - PubChem https://pubchem.ncbi.nlm.nih.gov/compound/Pasireotide
- Signifor® (pasireotide) Official Website for healthcare professionals outside the US http://www.signifor.com/
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2012/200677lbl.pdf
- http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Product_Information/human/002052/WC500128056.pdf
- "Novartis drug Signifor® approved in the EU as the first medication to treat patients with Cushing's disease". Retrieved 2012-07-08.
- Mancini, Tatiana; Porcelli, Teresa; Giustina, Andrea (2010). "Treatment of Cushing disease: overview and recent findings". Therapeutics and Clinical Risk Management. 6: 505–16. doi:10.2147/TCRM.S12952. PMC 2963160. PMID 21063461.
- EMEA Approval for Pasireotide
- "FDA Approves Pasireotide for Cushing's Disease".
- Tucker, Miriam E. FDA Approves Pasireotide for Treating Acromegaly, Medscape, December 17, 2014, Retrieved 2015-08-21
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