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Otto Schwarz, Chief Operating Officer, commented: "The significant clinical utility of Opsumit resulted in continued strong patient uptake with more than 21,000 patients currently receiving therapy. Moreover, after just one year on the US market, we can say that the Uptravi launch has been very successful by any standards, proving the high unmet medical need for oral prostacyclin therapy and validating our commercial strategy. I strongly believe that, as a part of the Johnson & Johnson family of companies, we will be able to serve even more patients by opening new markets and creating additional opportunities for our products."

André C. Muller, Chief Financial Officer, commented: "Actelion`s 2016 performance has been impressive with the company delivering record sales and earnings. The proposed transaction with Johnson & Johnson announced on 26 January will enable Actelion shareholders to not only monetize their holdings at 280 US dollars per share but also retain future upside potential with the distribution of 1 share in the newly created R&D company for every Actelion share. Both companies are now working to finalize the operational and financial details of the split and prepare the listing of the new company."

SALES UPDATE
Actelion`s excellent commercial performance during 2016 was driven by the outstanding Uptravi launch in the US and Opsumit`s sustained strong growth trajectory. During the fourth quarter of 2016, combined sales of the company`s outcome-based PAH portfolio - Opsumit, Uptravi and Veletri - reached 55% of total sales, demonstrating the significant progress made in the fundamental transformation of the PAH business.

In the US, sales increased by 25% at CER, driven by the strong Uptravi launch, the continued Opsumit momentum due to share gains in an expanding ERA market. European sales were 1% higher compared to 2015. A strong Opsumit performance and solid Tracleer use in the digital ulcer indication were impacted by continued pricing pressure and market erosion from bosentan generics, particularly in Spain. Sales in Japan increased by 19% at CER, driven by very strong sales of Opsumit (launched in June 2015), Tracleer momentum in the digital ulcer indication and Zavesca (Japanese trade name Brazaves).

Comparing average exchange rates for 2016 to 2015, the Swiss franc weakened, mostly against the US dollar, euro and Japanese yen, resulting in a positive currency variance of 63 million Swiss francs.

Sales by product - FY2016

*nm = not meaningful

Sales by product - Q4 2016

Sales by region - FY 2016

*Europe = EU28 and Switzerland

Sales by region - Q4 2016

*Europe = EU28 and Switzerland

PAH FRANCHISE
Opsumit^®
Sales of Opsumit (macitentan) amounted to 831 million Swiss francs for 2016, an increase of 57% at CER compared to 2015. The strong growth across all regions and all relevant markets (Opsumit is now available in almost 40 markets) was driven by solid quarterly increases in the number of patients treated in an expanding ERA market due to increased use in combination with PDE-5 inhibitors, and some upgrades from Tracleer, notably in Japan.

Uptravi^®
Sales of Uptravi (selexipag) amounted to 245 million Swiss francs for 2016. Since the US launch at the beginning of January 2016, patient demand has continued to increase with sales of 232 million Swiss francs (which includes 30 million Swiss francs for the build-up of inventory in the US). For the fourth quarter, US sales amounted to 77 million Swiss francs, compared to 66 million Swiss francs in the third quarter, 45 million Swiss francs in the second quarter and 15 million Swiss francs in the first quarter of 2016. In other geographies, Uptravi sales were driven by the particularly successful launch in Germany. Uptravi is also available in several other markets; it was most recently launched with full reimbursement in the Netherlands and Switzerland.

At the end of 2016, just over 2,400 patients were being treated with Uptravi globally, with more than 1,900 patients coming from the US.

Tracleer^®
Sales of Tracleer (bosentan) amounted to 1,020 million Swiss francs for 2016, a decrease of 18% at CER compared to 2015. This was driven to a large extent by volume erosion resulting from the significant impact of Opsumit uptake on the Tracleer patient base and by increased generic competition, notably in Spain, where generic bosentan entered the market in January 2016. Tracleer sales were supported by the digital ulcer indication in Europe and Japan.

Following the Pediatric Investigation Plan (PIP) compliance statement from the European Committee for Medicinal Products for Human Use (CHMP), applications for extension of the Supplementary Protection Certificate (SPC) were granted in all possible 19 EU countries until the end of August 2017.

Veletri^®
Sales of Veletri (epoprostenol for injection) amounted to 97 million Swiss francs for 2016, an increase of 12% at CER compared to 2015. This increase was mostly driven by France, Italy, Spain and the UK. Demand in Japan, where it is marketed as Epoprostenol ACT, remained strong, however sales growth was mitigated by a 12% price cut effective March 1, 2016. In February 2017, Actelion Pharmaceuticals Japan proudly announced that Epoprostenol ACT received a label extension for dosage and administration in pediatric patients with PAH.

Ventavis^®
Sales of Ventavis (iloprost) amounted to 73 million Swiss francs for 2016, a decrease of 32% at CER compared to 2015 due to competitive pressures, including the availability of Uptravi. Underlying units decreased by 37%.

SPECIALTY PRODUCTS
Valchlor^®
Sales of Valchlor (mechlorethamine) amounted to 35 million Swiss francs for 2016, an increase of 27% at CER compared to 2015. In the US, the company has made good progress in establishing Valchlor as a valuable option in the treatment algorithm for early-stage mycosis fungoides, a type of Cutaneous T-Cell Lymphoma (MF-CTCL).

In December 2016, the Committee for Medicinal Products for Human Use (CHMP), the scientific committee of the European Medicines Agency (EMA), issued a positive opinion for the use of chlormethine gel 160 micrograms/g (Ledaga®) for the treatment of mycosis fungoides-type cutaneous T-cell lymphoma (MF-CTCL) in adult patients and recommended that the European Commission approves the product. The European Commission is expected to issue a final decision by the end of February 2017.

Zavesca^®
Sales of Zavesca (miglustat) amounted to 104 million Swiss francs for 2016, an increase of 12% at CER compared to 2015.

Sales in the US were strong, due to a relatively low prior year base as a consequence of an inventory adjustment. In Europe, sales were flat due to the launch of generic miglustat (for the type 1 Gaucher disease indication only), which mitigated the continued strong, double-digit growth in the Niemann-Pick type C (NP-C) indication. Globally, the number of patients receiving Zavesca grew by 6%, compared to 2015, which was driven by a 13% increase in the treatment of patients with NP-C.

CORE R&D EXPENDITURE
The excellent commercial performance enabled Actelion to advance both the late and earlier stage pipeline, resulting in increased R&D expenditure which translates into a ratio of R&D core operating expenses to sales of 21%, slightly higher than in 2015. Core R&D expenses amounted to 509 million Swiss francs, an increase of 25% at CER. This increase was driven by higher clinical trial expenses, mainly driven by the strong recruitment in the Phase III OPTIMUM study (ponesimod in multiple sclerosis; announced in April 2015) and the Phase III IMPACT study (Cadazolid in Clostridium difficile associated diarrhea), as well as costs related to the preparation and initiation of Phase II studies for Actelion`s new ERA in specialty cardiovascular disorders and DORA in insomnia.

CORE OPERATING INCOME
Core operating income amounted to 992 million Swiss francs, an increase of 17% at CER.

CORE EPS
Diluted core earnings per share were CHF 8.18 for the full year 2016, an increase of 27% at CER compared to the same period of 2015.

DELIVERING VALUE TO SHAREHOLDERS
In-keeping with its commitment to maximizing shareholder value, Actelion returned 428 million Swiss francs to shareholders through the second-line share buyback as well as the increased dividend of CHF 1.50 per share, paid in May 2016. Actelion`s shares performed strongly throughout 2016 regardless of the extraordinary volatility created by the strategic discussions initiated in late November. The unaffected share price performance up until the strategic discussions became public was an increase of approximately 15%. At the end of the year, Actelion`s stock traded at 220.5 Swiss francs per share, an increase of 58% for the calendar year. The resulting total shareholder return (TSR) for 2016 amounted to 59%.

On 26 January 2017, Actelion and Johnson & Johnson jointly announced that they have entered into a definitive transaction agreement under which Johnson & Johnson will launch an all-cash tender offer in Switzerland to acquire all of the outstanding shares of Actelion for 280 US dollars per share. Additionally, Actelion shareholders will receive one share of a newly created R&D company that will be spun out concurrently with the closing of the proposed transaction.

CLINICAL DEVELOPMENT PIPELINE
The pipeline continued to strengthen with substantial progress made with several compounds:

• The ongoing Phase III program IMPACT investigating cadazolid treatment in patients suffering from Clostridium difficile-associated diarrhea is progressing well; results are expected in the first half of 2017.

• In the third quarter of 2016, Actelion announced the initiation of the Phase III POINT study, which investigates the use of combination therapy with ponesimod, an orally active, selective sphingosine-1-phosphate receptor 1 (S1P₁) immunomodulator, and dimethyl fumarate (Tecfidera^®) for patients with relapsing multiple sclerosis (RMS). The POINT study - which will be conducted under a Special Protocol Assessment (SPA) agreement with the FDA - is the first to assess the concurrent administration of two oral therapies in MS with the objective to improve disease control in this progressive, debilitating neurological disorder. Ponesimod is also being studied in the Phase III OPTIMUM study to compare the efficacy and safety of ponesimod with teriflunomide (Aubagio^®) in patients with RMS. The study is making good progress, with enrollment expected to be complete in Q1 2017.

• Also in the third quarter of 2016, the company advanced its new dual orexin receptor antagonist (DORA) into Phase II development in patients with insomnia. The Phase II program consists of two studies, one in adult and one in elderly patients, and is designed to evaluate the effect of Actelion`s DORA versus placebo on sleep maintenance and sleep initiation, as well as next-day residual effect and next-day performance. The study in adults also includes a zolpidem reference arm. The decision to move into a Phase II program was based on excellent data collected from the preclinical and Phase I clinical program, as well as a thorough understanding of the potential of dual orexin receptor antagonism on sleep efficacy and architecture.

• With macitentan (Opsumit), the company is conducting a pediatric study, TOMORROW, to evaluate the effect of macitentan on delaying disease progression in children with PAH using a pediatric formulation of macitentan. Recruitment is expected to start in Q1 2017.

• Actelion will assess the efficacy and safety of macitentan in stable Fontan-palliated adolescents and adults in the Phase III study RUBATO. The primary objective of this study is to assess the effect of macitentan as compared to placebo on exercise capacity through cardiopulmonary exercise testing (peak VO₂). The duration of the study is expected to be approximately 28 months; the start is planned for mid-2017.

• A Phase II study with macitentan, MERIT, assessed the efficacy, safety and tolerability of macitentan in patients with inoperable chronic thromboembolic pulmonary hypertension (CTEPH). The study was completed in September 2016 and delivered very positive results, meeting its primary endpoint of a significant reduction in pulmonary vascular resistance (PVR) with macitentan compared with placebo, and also showing a significant positive effect on exercise capacity for macitentan over placebo.

• A Phase III study with macitentan, MAESTRO, assessed the effects of macitentan on exercise capacity in patients with Eisenmenger Syndrome. The study was completed in January 2017, but did not meet the primary endpoint of significantly improving exercise capacity with macitentan compared with placebo.

• Lucerastat is being evaluated for the treatment of Fabry disease. In an initial Phase Ib study, patients receiving enzyme replacement therapy who were treated with lucerastat demonstrated a marked decrease in the accumulation of metabolic substrates thought to be responsible for the lesions characteristic of this disease. Actelion is currently in discussions with health authorities to move directly to Phase III.

¹ Upon completion of the proposed transaction these assets would be developed by Johnson & Johnson
² Upon completion of the proposed transaction these assets would be developed by the new R&D company

HUMAN RESOURCES
At the end of 2016, Actelion employed 2,624 permanent employees worldwide, an increase of 3% (or 77 permanent positions) compared to the end of 2015.

ANNUAL REPORT
Full details on the progress made in 2016 are available in Actelion`s 2016 Annual Report, at www.actelion.com/annual-report.

NOTES TO SHAREHOLDERS:
The next General Meeting of Shareholders will take place on or around 05 April, 2017, the date will be confirmed with the publication of the offer prospectus by Johnson & Johnson on or around 16 February 2017.

In light of the expected completion of the proposed transaction with Johnson & Johnson, the Board of Directors will propose to carry forward the 2016 accumulated profit and therefore not distribute any cash dividend.

RESULTS DAY CENTER
Investor community: To make your job easier, we provide links to all relevant documentation, such as a full financial review, reconciliation US-GAAP to Core results and geographical breakdown by product, from the Results Day Center on our corporate website: www.actelion.com/results-day-center.

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NOTES TO THE EDITOR

ABOUT ACTELION LTD.
Actelion Ltd. is a leading biopharmaceutical company focused on the discovery, development and commercialization of innovative drugs for diseases with significant unmet medical needs.

Actelion is a leader in the field of pulmonary arterial hypertension (PAH). Our portfolio of PAH treatments covers the spectrum of disease, from WHO Functional Class (FC) II through to FC IV, with oral, inhaled and intravenous medications. Although not available in all countries, Actelion has treatments approved by health authorities for a number of specialist diseases including Type 1 Gaucher disease, Niemann-Pick type C disease, Digital Ulcers in patients suffering from systemic sclerosis, and mycosis fungoides type cutaneous T-cell lymphoma.

Founded in late 1997, with now over 2,600 dedicated professionals covering all key markets around the world including Europe, the US, Japan, China, Russia and Mexico, Actelion has its corporate headquarters in Allschwil / Basel, Switzerland.

Actelion shares are traded on the SIX Swiss Exchange (ticker symbol: ATLN) as part of the Swiss blue-chip index SMI (Swiss Market Index SMI^®). All trademarks are legally protected by their respective owners.

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.

Financial Statements
Press release PDF
Financial Fact Sheet

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Source: Actelion Pharmaceuticals Ltd via GlobeNewswire
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