Last SFr.100.10 CHF
Change Today +1.75 / 1.78%
Volume 150.8K
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As of 11:43 AM 08/29/14 All times are local (Market data is delayed by at least 15 minutes).

santhera pharmaceuticals-reg (SANN) Snapshot

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08/29/14 - SFr.102.00
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09/2/13 - SFr.2.16
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santhera pharmaceuticals-reg (SANN) Details

Santhera Pharmaceuticals Holding AG, a specialty pharmaceutical company, is engaged in the discovery, development, and commercialization of pharmaceutical products for the treatment of mitochondrial and neuromuscular diseases in the areas of various orphan and niche indications in North America and the EU. The company offers Raxone/Catena for the treatment of Friedreich’s Ataxia. Its products under development include Raxone/Catena, which is in preparation for regulatory re-submission marketing authorization in Europe for Leber's Hereditary Optic Neuropathy, in a Phase III study for Duchenne Muscular Dystrophy, and in a Phase II study for Primary Progressive Multiple Sclerosis; omigapil that is in Phase I pharmacokinetics study in pediatric patients with Congenital Muscular Dystrophy; and Fipamezole, which has completed Phase IIb study for treatment of Dyskinesia in Parkinson's disease. Santhera Pharmaceuticals Holding AG was founded in 2004 and is headquartered in Liestal, Switzerland.

11.8 Employees
Last Reported Date: 04/7/14
Founded in 2004

santhera pharmaceuticals-reg (SANN) Top Compensated Officers

Chief Executive Officer
Total Annual Compensation: SFr.326.4K
Compensation as of Fiscal Year 2013.

santhera pharmaceuticals-reg (SANN) Key Developments

Santhera Pharmaceuticals Reports Positive Outcome for Catena(R)/Raxone(R) in Phase III DMD Trial Supported by Additional Respiratory Function Data

Santhera Pharmaceuticals reported that the results of secondary respiratory function endpoints from the on-going analysis of the DELOS trial in Duchenne Muscular Dystrophy (DMD) corroborate the positive outcome for the primary endpoint. These data provide further supportive evidence of a treatment benefit for Catena(R)/Raxone(R) in DMD. As previously announced, the DELOS trial met the primary endpoint, the difference between Catena(R)/Raxone(R) and placebo in the change from baseline to week 52 in Peak Expiratory Flow (PEF as percent predicted, PEF%p). Hospital-based spirometry assessments demonstrated that Catena(R)/Raxone(R) significantly reduced the annual decline in PEF%p by 66% compared to patients taking placebo. The average annual decline in PEF%p was 9.0% for placebo (Baseline: 54.3%; Week 52: 45.3% (n=27), p<0.001) versus 3.1% for Catena(R)/Raxone(R) (Baseline PEF%P: 53.1%; Week 52: 50.1% (n=30); p=0.13) for a treatment group difference in change from Baseline to Week 52 of 5.96% (p=0.04).

Santhera Pharmaceuticals Proposes to Amend Articles of Incorporation

Santhera Pharmaceuticals announced that at the Annual Shareholders' Meeting to be held on May 20, 2014, the company will propose to amend Article 8 of its Articles of Incorporation.

Santhera Pharmaceuticals Announces Consolidated Earnings Results for the Year Ended December 31, 2013

Santhera Pharmaceuticals announced consolidated earnings results for the year ended December 31, 2013. For the year, the company reported total revenue of CHF 1,319,000 compared to CHF 3,538,000 a year ago. Operating loss was CHF 7,309,000 compared to CHF 31,152,000 a year ago. Loss before taxes was CHF 5,760,000 compared to CHF 31,288,000 a year ago. Net loss was CHF 5,755,000 or CHD 1.55 per basic and diluted share compared to CHF 31,445,000 or CHD 8.55 per basic and diluted share a year ago. Cash flow used in operating activities was CHF 6,976,000 compared to CHF 11,039,000 a year ago.


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