Actelion to host Conference Call / Audiocast following the US FDA approval of Opsumit (macitentan) for the treatment of pulmonary arterial hypertension
Actelion Pharmaceuticals Ltd /
Actelion to host Conference Call / Audiocast following the US FDA approval of
Opsumit (macitentan) for the treatment of pulmonary arterial hypertension
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Dear member of the investment community,
Actelion Ltd will host a Conference Call / Audiocast on following the US FDA
approval of Opsumit®  (macitentan) for the treatment of pulmonary arterial
hypertension today, on Monday, 21 October 2013, at 14.00 CET / 13.00 BST /
08.00 a.m. EST.
The company announced on the 18 October 2013 that the United States Food and
Drug Administration (FDA) has approved the use of the orally available
endothelin receptor antagonist Opsumit® (macitentan) 10 mg once daily for the
treatment of pulmonary arterial hypertension (PAH) to delay disease progression.
Date/Time:
21 October 2013 14.00 hrs - 15.00 hrs Basel (CET)
 13.00 hrs - 14.00 hrs UK (BST)
 08.00 a.m. - 09.00 a.m. US (EST)
Conference Call Connect #:
Dial-in participants should start calling the number below 10-15 minutes before
the conference is due to start.
Dial: Europe: +41 (0)44 580 00 74
 UK: +44 (0)203 367 94 53
+1 866 907 59 23
 US:
Participant's mode:
Listen-Only with possibility to open individual lines during Q&A session.
Participants will be asked for their Name and Company.
Audiocast Access:
Audiocast participants should visit the Actelion website www.actelion.com 10-15
minutes before the conference is due to start.
Participant's mode:
Listen only
Audiocast Replay:
The archived Investor Audiocast will be available for replay through
http://www.actelion.com approximately 60 minutes after the call has ended.
For further information please contact:
Roland Haefeli
Senior Vice President, Head of Investor Relations & Public Affairs
+41 61 565 62 62
+1 646 737 49 72
http://www.actelion.com
Invitation PDF:
http://hugin.info/131801/R/1736798/582120.pdf
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originality of the information contained therein.
Source: Actelion Pharmaceuticals Ltd via Thomson Reuters ONE
[HUG#1736798]
