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Novartis Drug SOM230 is First Medical Therapy to Show Efficacy in a Phase III Trial in Cushing's Disease, a Debilitating Hormonal Disorder
Date:9/21/2010

a/. Accessed August 2010
  • European Medicines Agency. Committee for Orphan Medicinal Products public summary of positive opinion of orphan designation of pasireotide for the treatment of Cushing's disease. Oct 13, 2009
  • US Food and Drug Administration. For Industry: Orphan Drug Act. Available at: http://www.fda.gov. Accessed August 2010
  • ClinicalTrials.gov. Available at: http://www.clinicaltrials.gov. Accessed August 2010

  • Novartis OncologyMedia only:Investors only:Gloria Vanderham

    Richard JarvisNovartis Oncology

    Novartis CorporationP: +1 862 778 4268

    P: +1 212 830 2433M: +1 862 926 8420Dana Kahn CooperP: +1 732 817 1800M: +1 732 239 6664e-mail: media.relations@novartis.com

    e-mail: investor.relations@novartis.com
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