Catena: The Results of the Negotiated Agreement

Following correspondence with Health Canada and Santhera, we present the results of the negotiated agreement: Santhera formally commits to offering, and thus delivering, Catena to Canadian patients who are approved by Health Canada’s Special Access Programme (SAP). The price will remain about the same. Santhera can in no way influence...

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Santhera’s MICONOS Trial with Catena in Friedreich’s Ataxia Misses Primary Endpoint

Press Release Liestal, Switzerland, May 20, 2010 – Santhera Pharmaceuticals (SIX: SANN) announced today that its MICONOS Phase III study evaluating Catena®/Sovrima® for the treatment of Friedreich’s Ataxia missed its primary endpoint. Trends towards improvement in the key neurological endpoint were however identified by a meta-analysis of all Santhera’s Phase...

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Additional documents on Catena (Idebenon)

Some relevant information about Catena® (Idebenon) Catena®: Fact Sheet Catena®(idebenone): Product Monograph Catena®(idebenone): Product Monograph. Part III Actual Payer Coverage in Canada for CATENA® (Idebenon) Santhera Pharmaceuticals about preliminary results of the CATENA US clinical trial

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Health Canada Approves Catena® for Treatment of Friedreich’s Ataxia

News Release Liestal, Switzerland, July 24, 2008 – Santhera Pharmaceuticals (SWX:SANN), a Swiss specialty pharmaceutical company focused on neuromuscular diseases, announced today that Health Canada has approved with conditions SNT-MC17/idebenone for the treatment of Friedreich’s Ataxia. Health Canada’s decision is the first marketing authorization worldwide for any Friedreich’s Ataxia therapy....

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Cardiac problems in Friedreich’s Ataxia

Around 90% of patients afflicted with Friedreich’s Ataxia (FA) eventually show cardiac symptoms. In general, ataxia precedes the beginning of the cardiac symptoms. With most patients, it involves a cardiac disease called left ventricular hypertrophy. Left ventricular hypertrophy is an increase in the thickness of the wall and of the...

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