Orexo Interim Report Q2 2017
Financial overview Q2 2017
- Total net revenues SEK 159.1 million (188.2)
- Zubsolv® US net revenue SEK 124.1 million (112.8)
- EBIT SEK 9.8 million (12.1)
- EBITDA SEK 15.0 million (17.2)
- Earnings per share, before and after dilution, SEK 0.09/0.09 (0.14/0.14)
- Cash flow from operating activities SEK 48.7 million (20.0)
- Cash and cash equivalents SEK 294.3 million (252.9)
- Guidance of full year 2017 positive EBITDA is confirmed
Other highlights Q2 2017
- Orexo´s partner AstraZeneca advanced OX-CLI into clinical trials which triggered a milestone payment of USD 2.5 million
- Based on positive data a new project, OX382 - oral formulation, has been added to the pipeline
Financial overview YTD 2017
- Total net revenues SEK 286.4 million (339.2)
- Zubsolv US net revenue SEK 238.2 million (211.2)
- EBIT SEK -13.6 million (-14.1)
- EBITDA SEK -3.2 million (-2.3)
- Earnings per share, before and after dilution, SEK -0.91/-0.91 (-0.85/-0.85)
- Cash flow from operating activities SEK 76.9 million (42.5)
Continued strong financial performance
One of the important objectives for 2017 is to maintain company profitability and sustain our strong financial position, and I am pleased that the Q2 results demonstrate that we are progressing according to plan. In particular, our US business continues to improve, with Zubsolv® US showing a double digit growth (10 percent) in net sales from last year resulting in both positive profit and cash flow contributions in the second quarter on a Group level.
Another of my key objectives this year is to progress our pipeline. I am encouraged to see that during the second quarter our pipeline has made significant progress. The effort of developing the next generation of our drug delivery technologies has led to one specific project (OX382), an innovative oral formulation, progressing to late pre-clinical stage and is now ready for clinical phase I trial within the next 6 to 9 months. Furthermore, I am encouraged to see that the OX-CLI project, which is managed by our partner AstraZeneca, has progressed into clinical phase I. Our pipeline now has assets ranging from the exploratory phase to the registration phase consisting of six promising internal and partnered projects. The combined potential of these projects provides for new milestones and royalty streams as they evolve, in combination with future assets for our US organization to commercialize.
The US market for our lead product Zubsolv continues to show strong growth, but is also challenging with most of the growth coming from the public segment. Since Zubsolv currently has limited market access in the public segment in several of the growing geographies, it is a challenge to maintain overall market share. However, in the regions where Zubsolv has market access combined with field force coverage, Zubsolv continues to win market share and gain volume. In this market environment, I appreciate that we have managed to grow our net sales year over year and gain volume, although we need to and are focused on improving our ability to compete in the fast growing public segment.
The critical success factor to be able to compete in the public segment is price. Consequently, we have increased the investment in our market access efforts and adjusted our overall marketing mix to optimize the balance between growth and profitability. To improve profitability and competitiveness improved effectiveness of our supply chain has become a key success factor. I am very pleased with the progress we are making in our supply chain and we will be able to significantly reduce our cost of goods sold. We are still finalizing the details of our supply chain for 2018 and beyond, but applying the anticipated future manufacturing cost of Zubsolv to the 2016 result, would have more than doubled our net earnings.
Continuing to look forward I am confident that our efforts regarding market access will start to pay off. Most of the existing formulary positions have been confirmed for 2018, to date none have been removed and we have also gained new contracts effective from 2018. Additionally we are making good progress in current negotiations which can further improve our ability to capture the strong growth that characterizes our main market. The journey of developing a growing profitable pharmaceutical company has just begun, enabling a strong financial platform for continued investment in the evolution of Orexo. The strong financial performance, positive signs in market access for 2018 in the US and the pipeline progress in Q2 are important indications that we are heading in the right direction.
President and CEO
|For further information, please contact|
|Nikolaj Sørensen, President and CEO||Henrik Juuel, EVP and CFO|
|Tel +46 18 780 88 00||Tel +46 18 780 88 00|
|E-mail i firstname.lastname@example.org||E-mail email@example.com|
|At 2 pm, the same day as the announcement of the report, Orexo invites analysts, investors and media to attend an audiocast with a web presentation where Nikolaj Sørensen, CEO, and Henrik Juuel, CFO, will present the report. After the presentation a Q&A will be held. Questions can also be sent in advance to
, no later than 11.00 am CET. Please view the instructions below on how to participate.
Internet: http://tv.streamfabriken.com/orexo-q2-2017. Telephone: (SE) +46 8 566 426 92, (UK) +44 20 300 89 807 or (US) +1 855 831 5945. The presentation material will be available on Orexo´s website one hour prior to the audiocast.
This information is information that Orexo AB (publ.) is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact persons set out above, at 8.00 am CET on July 11, 2017.