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February 13, 2016 11:28 AM ET

Pharmaceuticals

Company Overview of Sigma-Tau Pharmaceuticals, Inc.

Company Overview

Sigma-Tau Pharmaceuticals, Inc. is a research-based pharmaceutical company that focuses on the discovery of molecules and therapies to help improve the lives of people who suffer from rare diseases in Canada. The company develops prescription pharmaceuticals, including Cystaran, a cysteamine ophthalmic solution; Carnitor levocarnitine tablets, oral solution, sugar-free oral solution, and injection; Carnitor, a levocarnitine injection; Matulane procarbazine hydrochloride capsules; Adagen, a pegademase bovine; Abelcet, an amphotericin B lipid complex injection; and DepoCyt, a cytarabine liposome injection. It also develops nonprescription medicines and dietary supplements. The company was foun...

9841 Washingtonian Boulevard

Suite 500

Gaithersburg, MD 20878

United States

Founded in 1980

Phone:

301-948-1041

Fax:

301-948-1862

Key Executives for Sigma-Tau Pharmaceuticals, Inc.

Chief Executive Officer
Vice President of Finance
Chief Executive Officer of Sigma-Tau Group
Vice President of Medical Affairs
Vice President of Clinical Affairs
Age: 59
Compensation as of Fiscal Year 2015.

Sigma-Tau Pharmaceuticals, Inc. Key Developments

Sigma-Tau Pharmaceuticals, Inc. Receives Orphan Drug Designation for STP-206 for Prevention of Necrotizing Enterocolitis

Sigma-Tau Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration (FDA) has granted an orphan drug designation for the company's investigational compound, STP-206 (lactobacillus acidophilus and Bifidobacterium animalis subsp. lactis), a live biotherapeutic being developed for the prevention of necrotizing enterocolitis (NEC) in premature infants with very low birth weight less than or equal to 1,500 grams. The company is currently conducting a multi-center, double-blind, randomized, placebo-controlled Phase 1b/2a clinical trial for STP-206 at a number of different sites in the United States. An Orphan drug designation is granted by the FDA Office of Orphan Products Development to novel drugs that treat a rare disease or condition affecting fewer than 200,000 patients in the U.S. The designation provides the beneficiary company with a seven-year period of U.S. marketing exclusivity if it is the first product to reach marketing approval, as well as potential tax credits for clinical research costs, federal grants, and a waiver of Prescription Drug User Fee Act (PDUFA) filing fees.

Sigma-Tau Pharmaceuticals Names Dave Lemus as Chief Executive

Sigma-Tau Pharmaceuticals appointed Dave Lemus as chief executive.

Sigma-Tau Pharmaceuticals, Inc. Signs License Agreement with Crosscare Limited

Sigma-Tau Pharmaceuticals, Inc. announced that it has signed an exclusive United States license agreement with Crosscare Limited to market and distribute Colief Infant Drops for the treatment of colic. Under the multi-year license agreement, Sigma-Tau will be responsible for the sales, marketing and distribution of Colief in the United States.

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