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Actelion announces commercial availability of Uptravi (selexipag) in Germany...

(Source: Actelion Ltd) Market authorization for treatment of pulmonary arterial hypertension granted by European Commission on 12 May 2016 Uptravi available for patients in Germany as of 15 June 2016...

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Actelion announces US commercial availability of UPTRAVI (selexipag) as of 4...

(Source: Actelion Ltd) UPTRAVI - FDA approved on 21 December 2015 for treatment of pulmonary arterial hypertension (PAH, WHO Group 1) to delay disease progression and reduce the risk of hospitalization...

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Actelion receives approval for Uptravi (selexipag) for the treatment of...

(Source: Actelion Ltd) Approval granted by Medsafe in New Zealand on 17 March 2016 and by the TGA in Australia on 18 March 2016 ALLSCHWIL, SWITZERLAND - 22 March 2016 - Actelion Ltd (SIX: ATLN)...

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Actelion receives Health Canada approval for Uptravi (selexipag) for the...

(Source: Actelion Ltd) ALLSCHWIL, SWITZERLAND - 26 January 2016 - Actelion (SIX: ATLN) announced today that Health Canada has granted a Notice of Compliance (NOC) approving the orally active, selective...

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Eisai Demonstrates Efficacy of Investigational Dual Orexin Receptor...

Presented at 53rd American College of Neuropsychopharmacology Annual Meeting Tokyo, Dec 10, 2014 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") announced today that...

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Actelion is granted marketing authorization for Uptravi (selexipag) in...

(Source: Actelion Ltd) Marketing authorization granted by European Commission on 12 May 2016 First European Union (EU) market introduction to commence in the near future ALLSCHWIL, SWITZERLAND - 17 May...

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Actelion delivers excellent results in the first quarter 2015 (Actelion Ltd)

(Source: Actelion Ltd) ALLSCHWIL/BASEL, SWITZERLAND - 21 April 2015- Actelion Ltd (SIX: ATLN) today announced its results for the first quarter of 2015. OPERATING HIGHLIGHTS Opsumit (macitentan) - Q1...

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Actelion advances clinical development of its specialty immunology pipeline...

(Source: Actelion Ltd) ALLSCHWIL/BASEL, SWITZERLAND - 16 April 2015 - Actelion Ltd (SIX: ATLN) announced today that it is accelerating its clinical development efforts in the field of immunological...

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Actelion receives positive CHMP opinion for Uptravi (selexipag) for the...

(Source: Actelion Ltd) The European Commission is expected to make a final decision within 67 days. ALLSCHWIL, SWITZERLAND - 29 January 2016 - Actelion (SIX: ATLN) announced today that the Committee...

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Desperately Seeking Shut-Eye

In the early 1970s, a colleague of Stanford Universityā€™s William Dement remarked on the resemblance of a narcolepsy patientā€™s symptoms to those of a recent canine patient he had read about. The...

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Actelion receives US FDA approval of Uptravi (selexipag) for the treatment of...

(Source: Actelion Ltd) Uptravi approved for treatment of pulmonary arterial hypertension (PAH, WHO Group 1) to delay disease progression and reduce the risk of hospitalization for PAH Uptravi will be...

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Selexipag (Uptravi) data in pulmonary arterial hypertension to be presented...

(Source: Actelion Ltd) ALLSCHWIL, SWITZERLAND - 02 March 2015 - Actelion Ltd (SIX: ATLN) today announced that key data from the pivotal Phase III selexipag (UptraviĀ®) study will be shared during an...

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Actelion delivers excellent first half 2015 results (Actelion Ltd)

(Source: Actelion Ltd) ALLSCHWIL/BASEL, SWITZERLAND - 21 July 2015- Actelion Ltd (SIX: ATLN) today announced its results for the first six months of 2015. OPERATING HIGHLIGHTS OpsumitĀ® - Sales of CHF...

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Actelion's New Drug Application for selexipag (Uptravi) is accepted by the US...

(Source: Actelion Ltd) ALLSCHWIL, SWITZERLAND - 03 March 2015 - Actelion Ltd (SIX: ATLN) today announced the formal acceptance of the New Drug Application (NDA) for selexipag (UptraviĀ®) by the US Food...

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Actelion submits selexipag (Uptravi) for EMA Marketing Authorisation in...

(Source: Actelion Ltd) ALLSCHWIL, SWITZERLAND - 02 December 2014 - Actelion Ltd (SIX: ATLN) today announced the submission of a centralized Marketing Authorisation Application (MAA) to the European...

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Very strong performance continues in the first quarter of 2016 - driven by...

(Source: Actelion Ltd) ALLSCHWIL/BASEL, SWITZERLAND - 21 April 2016- Actelion Ltd (SIX: ATLN) today announced its results for the first three months of 2016. OPERATING HIGHLIGHTS Excellent Opsumit...

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Selexipag meets primary endpoint in pivotal Phase III GRIPHON outcome study...

(Source: Actelion Ltd) ALLSCHWIL, SWITZERLAND - 16 June 2014 - Actelion Ltd (SIX: ATLN) today announced the top-line results of the pivotal Phase III GRIPHON study in 1,156 patients with pulmonary...

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Actelion submits US FDA New Drug Application for selexipag (Uptravi) in...

(Source: Actelion Ltd) ALLSCHWIL, SWITZERLAND - 23 December 2014 - Actelion Ltd (SIX: ATLN) today announced that it has submitted a New Drug Application (NDA) to the US Food and Drug Administration...

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Actelion initiates Phase III study to evaluate macitentan (Opsumit) in...

(Source: Actelion Ltd) Phase III study TOMORROW aims to show the long-term benefits of macitentan (Opsumit) in children with pulmonary arterial hypertension (PAH) Global program has received...

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Actelion delivers strong nine months results (Actelion Ltd)

(Source: Actelion Ltd) ALLSCHWIL/BASEL, SWITZERLAND - 20 October 2015 - Actelion Ltd (SIX: ATLN) today announced its results for the first nine months of 2015. OPERATING HIGHLIGHTS Opsumit (macitentan)...

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