Publication of Idorsia's prospectus relating to the listing of Idorsia Ltd on SIX Swiss
Exchange


Actelion Pharmaceuticals Ltd /
Publication of Idorsia's prospectus relating to the listing of Idorsia Ltd on 
SIX Swiss Exchange 
. Verarbeitet und übermittelt durch Nasdaq Corporate Solutions.
Für den Inhalt der Mitteilung ist der Emittent verantwortlich.
Source: Globenewswire

ALLSCHWIL/BASEL,  SWITZERLAND  -  09 June  2017 -  Actelion Ltd (SIX:ATLN) today
published  the listing prospectus  relating to the  listing of Idorsia shares on
SIX  Swiss  Exchange.  With  the  tender  offer  for all publicly held shares of
Actelion  Ltd by Janssen Holding  GmbH, a Swiss subsidiary  of Johnson & Johnson
(J&J)  for Actelion on track for completion,  it is expected that the settlement
of  the  tender  offer  by  J&J  will  take  place on 16 June 2017. The demerger
distribution,  approved by the General Meeting  of Actelion Shareholders held on
5 April  2017, will take  place concurrently,  whereby all Actelion shareholders
(whether  they tendered their shares or not)  will receive one Idorsia share per
each  Actelion share  held on  13 June 2017. It  is expected that Idorsia shares
will be listed and commence trading on SIX Swiss Exchange on 16 June 2017.

About Idorsia Ltd
Idorsia  will  be  an  independent  biopharmaceutical company specialized in the
discovery  and development of small molecules  to meet significant unmet medical
needs.  Idorsia  will  have  a  diverse clinical development pipeline comprising
several  compounds being  investigated in  multiple therapeutic areas, including
central   nervous  system  disorders,  cardiovascular  disorders,  immunological
disorders  and orphan diseases. Idorsia  will inherit Actelion's established and
validated  drug discovery engine  and a strong  cross-section of its development
organization.  Idorsia's  pipeline  will  continue  to  be developed by selected
members of Actelion's development organization who joined Idorsia.

Headquartered  in Allschwil,  Switzerland, Idorsia  was incorporated  on 2 March
2017 and will employ over 600 employees.

Idorsia's key strengths lie in the unique combination of:
  * Skills: An experienced team comprising over 600 employees, with a proven
    track record of successfully bringing drug candidates to market
  * Products: Ownership of a clinical pipeline of drug candidates in different
    areas of medicine where patients' needs are not fully met with existing
    therapies
  * Assets: State-of-the-art facilities
  * Cash: Financing with CHF 1 billion in cash. Additionally, Cilag, a
    subsidiary of Johnson & Johnson, will provide Idorsia with a CHF Credit
    Facility equivalent to USD 250 million


Idorsia's development pipeline
Idorsia will have a diverse clinical development pipeline comprising several
compounds being investigated in multiple therapeutic areas, including central
nervous system disorders, cardiovascular disorders, immunological disorders and
orphan diseases.

Idorsia's  drug  discovery  will  focus  on  novel  molecular  target  families,
implementing  appropriate  state-of-the-art  technologies.  In  particular,  the
target  families will include G-protein  coupled receptors (GPCRs), ion channels
and certain enzymes.

 Status     Compound       Mechanism of Action          Target Indication
---------- -------------- ---------------------------- ------------------------
            Aprocitentan   Endothelin receptor          Resistant hypertension
            (ACT-132577)   antagonist
           -------------- ---------------------------- ------------------------
            ACT-541468     Dual orexin receptor         Chronic insomnia
                           antagonist
 Phase 2   -------------- ---------------------------- ------------------------
                           Endothelin receptor          Vasospasm associated
            Clazosentan    antagonist                   with aneurysmal
                                                        subarachnoid hemorrhage
           -------------- ---------------------------- ------------------------
            Cenerimod      S1P(1) receptor modulator    Systemic lupus
                                                        erythematosus
---------- -------------- ---------------------------- ------------------------
 Phase 1b   Lucerastat     Glucosylceramide synthase    Fabry disease
                           inhibitor
---------- -------------- ---------------------------- ------------------------
            ACT-246475     P2Y12 receptor antagonist    Acute coronary
syndrome
           -------------- ---------------------------- ------------------------
            ACT-774312     CRTH2 receptor antagonist    Asthma and allergy
                                                        disorders
 Phase 1   -------------- ---------------------------- ------------------------
            ACT-539313     Selective orexin 1           Anxiety
                           receptor antagonist
           -------------- ---------------------------- ------------------------
            ACT-709478     T-type calcium channel       Epilepsy
                           blocker
---------- -------------- ---------------------------- ------------------------

Corporate Governance
Idorsia's  Board of  Directors comprises  Jean-Pierre Garnier (Chairman), Robert
Bertolini  (member, Chair Finance & Audit committee), Jean-Paul Clozel (member),
John J. Greisch (member, Chair Nominating, Governance & Compensation committee),
David Stout (member) and Herna Verhagen (member).

Idorsia's  Executive  Committee  consists  of  Jean-Paul Clozel (Chief Executive
Officer),  Guy Braunstein (Head of  Global Clinical Development), Martine Clozel
(Chief Scientific Officer) and André C. Muller (Chief Financial Officer).


Indicative timetable of events
All dates listed below represent Idorsia's current expectations of the timing of
key  events in connection with the listing  of Idorsia shares and are subject to
change.

 Event                                                            Expected Date
-------------------------------------------------------------------------------
 Cut-off Date for entitlement to receive dividend in kind         13 June 2017
-------------------------------------------------------------------------------
 Ex-dividend date                                                 14 June 2017
-------------------------------------------------------------------------------
 Record date                                                      15 June 2017
-------------------------------------------------------------------------------
 Distribution of the Main Shares and Settlement                   16 June 2017
-------------------------------------------------------------------------------
 Listing and First Day of Trading of the Main Shares on SIX       16 June 2017
-------------------------------------------------------------------------------
 Listing and First Day of Trading of the Authorized Shares on SIX 20 June 2017
-------------------------------------------------------------------------------

The  listing prospectus can be accessed  by Actelion's shareholders via internet
on     Actelion's     website    https://www.actelion.com/en/investors/proposed-
transaction/index.page

                                      ###
Notes to the Editor

Actelion's financial statements for the first quarter of 2017
In  order to prepare the pro-forma  financial information for Idorsia, the first
quarter  financial statements for Actelion were used  as a baseline. They can be
found in the financial archive at:
https://www.actelion.com/en/investors/financial-information/financial-
archive.page?

Collaboration Agreement with Janssen Biotech, Inc.
Idorsia  and  Janssen  Biotech,  Inc.,  a  subsidiary of Johnson & Johnson, have
entered  into a Collaboration Agreement giving  Janssen Biotech, Inc. the option
to  collaborate  with  Idorsia  to  jointly  develop  and  solely  commercialize
aprocitentan  (ACT-132577) and  any  of  its  derivative  compounds or products.
Aprocitentan  is being  investigated for  use in  resistant hypertension and has
completed a dose-finding study in essential hypertension. Following the later of
the end of the Phase 2 study meeting with the FDA or receipt by Janssen Biotech,
Inc.  of a complete Phase 2 data package, Janssen Biotech, Inc. will have thirty
days to opt in to the collaboration by paying Idorsia a milestone payment of USD
230 million.  In  addition,  under  the  terms  of  the Collaboration Agreement,
Janssen  Biotech,  Inc.  will  pay  Idorsia  royalties  on  products  containing
aprocitentan.

Revenue Sharing Agreement with Johnson & Johnson
Idorsia  Pharmaceuticals Ltd, J&J and  Actelion Pharmaceuticals Ltd have entered
into  a Revenue Sharing  Agreement in respect  of ponesimod and cadazolid. Under
the terms of the Revenue Sharing Agreement, if market authorization is obtained,
Idorsia  Pharmaceuticals Ltd is entitled to  receive quarterly payments of 8% of
the  aggregate  net  sales  of  ponesimod  and  cadazolid products from Actelion
Pharmaceuticals  Ltd. For each of ponesimod and cadazolid, payments will be made
under  the Revenue Sharing Agreement for fifteen years from the latest launch of
a  product containing ponesimod  or cadazolid (as  applicable) in (i) the United
States,  (ii) Canada or  (iii) any one  of the United  Kingdom, France, Germany,
Italy and Spain.

For further information please contact:
Andrew Weiss
Senior Vice President, Head of Investor Relations & Corporate Communications
Actelion Pharmaceuticals Ltd, Gewerbestrasse 16, CH-4123 Allschwil
+41 61 565 62 62
www.actelion.com

The above information contains certain "forward-looking statements", relating to
the  company's business, which  can be identified  by the use of forward-looking
terminology  such as  "estimates", "believes",  "expects", "may",  "are expected
to",  "will",  "will  continue",  "should",  "would  be",  "seeks", "pending" or
"anticipates"  or similar expressions,  or by discussions  of strategy, plans or
intentions. Such statements include descriptions of the company's investment and
research  and development  programs and  anticipated expenditures  in connection
therewith, descriptions of new products expected to be introduced by the company
and  anticipated customer demand for such products and products in the company's
existing  portfolio. Such  statements reflect  the current  views of the company
with  respect to future  events and are  subject to certain risks, uncertainties
and  assumptions. Many  factors could  cause the  actual results, performance or
achievements  of the company to be materially different from any future results,
performances  or achievements that may be  expressed or implied by such forward-
looking  statements.  Should  one  or  more  of  these  risks  or  uncertainties
materialize,  or should  underlying assumptions  prove incorrect, actual results
may  vary  materially  from  those  described  herein  as anticipated, believed,
estimated or expected.

Press release PDF: 
http://hugin.info/131801/R/2112066/803251.pdf



This announcement is distributed by Nasdaq Corporate Solutions on behalf of Nasdaq Corporate
Solutions clients.
The issuer of this announcement warrants that they are solely responsible for the content,
accuracy and originality of the information contained therein.
    
Source: Actelion Pharmaceuticals Ltd via GlobeNewswire

http://www.actelion.com