Kåre Schultz1:52
Thanks, Kevanix. Welcome everyone and thanks for your interest in Teva. Our Q3 2021 financial highlights will start focusing on our revenues. The revenues came in stable compared to last year, but with a lot of underlying dynamics which I'll be reviewing in the following slides. Our adjusted EBITDA came in at 1.2 billion US dollars, also very stable compared to a year ago. All-in EPS came in at 26 cents. Non-GAAP diluted EPS came in at 59 cents, also very close to last year. Free cash flow came in strongly at 795 million dollars. We continue to see debt reduction and net debt has now been reduced to 21.7 billion dollars. Today we also announced a 4 billion dollar refinancing. It's a debt-neutral refinancing and it's issuing sustainability-linked bonds which are linked to environmental KPIs and to access KPIs. Of course, we believe that by being the leading generic company in the world, we have a special, you could say, ability to support low and middle-income countries with essential medicines, and we believe that's a very strong commitment we're showing with this bond offering. If we move to the next slide, and here you can see some other dynamics on the revenue side. I'll just highlight a few of them. If you look at North America, you can see that North American revenue is a little bit below what it was a year ago. It's basically driven by the usual suspects, you could say, which is that Copaxone is declining and we have Ajovy and Austedo increasing, and I'll be commenting on the increase of Ajovy and Austedo in the coming slides. If you look at Europe, you can see that Europe is up compared to a year ago. We have seen some fluctuations, as you know, in Europe due to the COVID-19 pandemic, so we saw lower volumes in the first and second quarter of this year. We're seeing volumes starting to pick up again here in the third quarter, and we expect volumes to continue to increase in the fourth quarter. In international markets, we're basically more or less unchanged, and that really means that the key drivers here, as I said, Copaxone, Ajovy, and Austedo. So let's move to the next slide. Here you can see the development for Austedo in the US. As you can see, we have seen a nice, strong growth in the last three quarters, but you can also see that there was a COVID-related slowdown in the growth, and that was really because patients were going to their psychiatrist more, psychiatrist offices were closed during the lockdowns, and therefore we saw this slowdown that you see in the revenues here in the first and the second quarter. We are back on a strong growth track now. You can see that both on the total scripts to the left, and you can see it also on the revenue numbers. This is a development that we expect will continue. And of course, we are also focusing very much on patient activation and our DTC campaign to ensure that more people with tardive dyskinesia can get on therapy. We still estimate that there's around 500,000 people suffering from tardive dyskinesia in the US, and only a very small fraction of this patient population is currently being treated. So we are very optimistic about the future growth of Austedo. If we move to the next slide, then as you know, Ajovy is launched now in most of the European countries and has been launched in the US for several years. And with regard to Austedo, we see a continued nice development in the US in the terms of our total scripts growing quarter over quarter, and we also see a very nice development on Ajovy in Europe with volumes growing steadily also quarter after quarter. We had an initial ambition of 25% market share in US and Europe for Ajovy. We increased that ambition, I think, one or two quarters ago to a third of the market, and we still believe it's very likely that we can reach a third of the market. And that's basically due to the very superior long-acting profile of the drug, which means that it can be dosed both monthly and quarterly, and a very good safety profile that we have. So, strong development with Ajovy. Also, as you'll note in the total sales numbers, we had a milestone in Japan, which is very positive because that's related to the actual launch of Ajovy in Japan, and that means that in the coming quarters we will have revenue from North America, Europe, and Japan in the Ajovy numbers. So, let's move on to the next slide. Here we're showing you our specialty and biosimilar R&D pipeline, product pipeline. We're very happy with it. I won't go through it all, that would take too long, but let me just mention two interesting projects. One is respiratory LAI, long-acting risperidone, which has been accepted by FDA. Our file has been accepted for review. We hope to have it approved next year. This is a major new benefit for people suffering from schizophrenia in the form of a subcutaneous injectable long-acting risperidone. So we look forward to bringing that to the market to the benefit of people suffering from schizophrenia. We also have a new interesting license arrangement, and it's shown here in phase one, AL 138B. And if we move to the next slide, then I'll just tell you a little bit about that. We have made a license agreement with Modag, a German company, and it's regarding two compounds that are in the development for treatment of MSA and Parkinson's disease. And we're very excited about this. As you know, we have a long history in Parkinson's. We think these projects are very, very interesting, and hopefully, long-term, if they turn out to work, then they could also have a potential in treatment of Alzheimer's. So that's a really exciting addition to our portfolio. Let's move to the next slide. As you know, we have a long-term target for our operating margin of 28%. And during our restructuring with the loss of capacity, of course, we saw operating margin decline, and then we turned around in 2019, and now we're growing the margin. And I'm happy to report that we were growing, we're growing the margin in line with our expectations. You can see here, yesterday, 26.3, it's 26.8, and if you take the midpoint of our guidance, it's 27.5. And we're still committed to the target at the end of 2023 of 28%. The next slide. It's actually today, very close to exactly four years since I joined Teva, and I'm very happy to report that in those four years we reduced the debt by some close to 13 billion, 12-13 billion dollars. And we've actually also paid 4 billion dollars in interest rates in those four years altogether. So something like close to 16-17 billion dollars have been returned to the bondholders, and we'll continue to do that because, as you can see on the next slide, we have our unchanged long-term financial targets. We want to take the net debt to EBITDA below three times at the end of '23, and in order to do so, we need cash earnings to be strong, above 80%, and we need the operating income margin, as I said before, to be at 28% so that we generate the cash needed to basically keep on reducing the debt. And we are committed to use the cash flow for debt reduction, and we have no plans of raising equity. And on that note, I'll hand over to Eli Kalif.