April 12, 2018: Santhera’s Shareholders Approve all Board Proposals at Today’s Annual General Meeting
April 05, 2018: Santhera Announces Successful Completion of First Clinical Trial with Omigapil in Patients with Congenital Muscular Dystrophy
March 20, 2018: Santhera Reports Solid Top-line Growth in 2017 and Reiterates its Strategy to Obtain Approval for Idebenone in Duchenne Muscular Dystrophy
March 05, 2018: Santhera Reports Outcome of Exploratory Trial with Idebenone in PPMS Conducted at the NIH
February 15, 2018: Santhera Obtains Worldwide Exclusive License from Polyphor to Develop and Commercialize Clinical Stage Candidate for Cystic Fibrosis and Other Pulmonary Diseases
February 06, 2018: Santhera Launches U.S. Expanded Access Program with Idebenone for Patients with Duchenne Muscular Dystrophy (DMD)
January 29, 2018: Santhera Reports Preliminary Key Financial Figures for 2017 and Provides Corporate Update Conference Call 14:00 hrs CET (audio file mp3)
January 26, 2018: Santhera Receives Negative CHMP Opinion on Appeal for Authorization of Raxone® in Duchenne Muscular Dystrophy Conference Call 14:00 hrs CET (audio file mp3)
January 24, 2018: Santhera Anticipates Receiving a Negative CHMP Opinion on Appeal for Marketing Authorization Application for Raxone® in Duchenne Muscular Dystrophy
January 19, 2018: Santhera Plans to Announce Regulatory Feedback for Raxone® in DMD and 2017 Preliminary Key Financial Figures