Pfizer Q1'16 Earnings Conference Call: Full Transcript

Operator:

Good day everyone and welcome to Pfizer’s First Quarter 2016 Earnings Conference Call. Today’s call is being recorded. At this time I would like to turn the call over to Mr. Chuck Triano, Vice President of Investor Relations. Please go ahead.

 

Chuck Triano:Investor Relations:

Thank you. Good morning and thanks for joining us today to review Pfizer’s first quarter 2016 performance and 2016 financial guidance. I am joined today by our Chairman and CEO, Ian Read; Frank D’Amelio our CFO; Mikael Dolsten President - Worldwide Research and Development; Albert Bourla President of Pfizer Innovative Pharma; John Young, President of Established Pharma and Doug Lankler, General Counsel.

The slides that will be presented on the call can be viewed at our homepage pfizer.com by clicking on the link for Pfizer quarterly corporate performance first quarter 2016 which is located in the For Investors section in the lower right hand corner of this page.

Before we start I would like to remind you that our discussion during the call will include forward-looking statements that are subject to the risks and uncertainties that could cause actual results to differ materially from those projected in the forward-looking statements. Additional information regarding these factor is discussed under the disclosure notice section in the earnings release we issued this morning as well as in our 2015 annual report on Form 10-K including in part one item 1A risk factors that is filed with the Securities and Exchange Commission and is available at their website sec.gov and our website pfizer.com.

Forward-looking statements during this conference call speak only as of the original date of this call and we undertake no obligation to update or revise any of these statements. -- also includes certain financial measures that were not prepared in accordance with US Generally Accepted Accounting Principles. Reconciliation of those non-GAAP financial measures to the most directly comfortable GAAP financial measures can be found in Pfizer’s current report on Form-8-K dated today May 3, 2016. You may obtain a copy of the Form-8-K on our website pfizer.com/investors.

Also any non-GAAP measures presented are not and should not be viewed as substitutes for financial measures required by US GAAP has no standardized meaning prescribed by US GAAP and may not be comfortable to the calculations of similar measures at other companies. We will now make prepared remarks and then we will move to a Q&A session.

With that I will now turn the call over Ian Read. Ian?

 

Ian Read:Chairman and Chief Executive Officer:

Thank you Chuck and good morning everyone. To my remarks this morning I will briefly recap the highlights from the quarter and comment on our strategies including expected pipeline development this year, our approach to business development in light of our decision not to move forward with Allergan and the steps we expect to take to assess the potential split of the company .

2016 is off to a good start with solid performance across both the Innovative and Established businesses notably Prevnar 13, Ibrance, Eliquis, and Chantix, are performing better than we initially projected. As we referenced in our earnings release, a portion of the growth in the quarter was attributable to additional selling days compared to the year-ago quarter which will be offset in the fourth quarter from the growth perspective. We nonetheless had a strong quarter financially even with that impact exceeding our internal projections and incorporated the strong operational performance as well as the recent weakening of the dollar into our updated financial guidance for the year. And compared to the first quarter we expect that our LOE impact from Lyrica, Rebif, Enbrel, will be more pronounced in the remaining quarters of the year.

Additionally, new product launch expenses and R&D investment are also said higher for the remainder of the year. Frank will provide more details in a few minutes. Overall looking at the quarter, on a revenue to size a standalone business excluding Hospira grew 15% operationally and 26% operationally with inclusion of Hospira. Our Innovative business generated impressive operational revenue growth of 28% driven by the performance of Eliquis globally and Ibrance, Prevnar 13, Lyrica, Xeljanz, Chantix and -- 24 hour principally in the US.

Of particular note, Ibrance has already earned broad patient and physician acceptance. Since launching in the US last year of 6,800 prescribers have treated approximately 28,000 women with HR positive HER2 negative metastatic breast cancer and the feedback continues to be very encouraging particularly around the efficacy and tolerability profile and impact on the overall quality of life.

Recently we announced that the confirmatory Phase 3 PALOMA-2 trial for Ibrance in first line metastatic breast cancer met its primary end points of improving progression free survival. Detail result will be presented at ASCO in early June.

We are also seeing continued strong operational growth from Eliquis which is yielding increased market penetration and market share gains in the US and Japan. The contribution of Eliquis to our alliance revenue line more than doubled year-over-year. For the Prevnar 13 Adult indication while there was year-over-year growth as expected, we saw a sequential quarterly decline in revenues given the rapid penetration we achieved in the US market June 2015. The pediatric indication that remained strong and we anticipate that global revenues for the Prevnar 13 franchise in full year 2016 will be comparable to 2015 and we were pleased that the results in the EAGLES study, the largest global clinical trial in smoking cessation medicines, were published in the The Lancet.

-- and the compare the neuropsychiatric events with Chantix and bupropion with placebo and nicotine patch in adult smokers with and without a history of psychiatric disorders. The office concluded that the study did not show a significant increase in serious neuropsychiatric events with Chantix or bupropion relative to placebo or nicotine patch. The study also found that smokers treated with Chantix had significantly higher quit rates than those treated bupropion nicotine patch or placebo.

Turning to our Established business. It grew 24% operationally primarily due to the additional revenues from legacy Hospira products. Without Hospira and the impact of foreign exchange the business grew 1% and particularly particular we saw strong performance on the sterile injectables portfolio. The addition of Hospira’s leading generic and portfolio were Pfizer’s legacy branded injectables established as Pfizer’s the number one in sterile injectables company globally.

We now have one of the broadest and most diverse offerings ability to manufacture sterile injectable medicines which are critically important for patients around the world.

This leading market position combined with our expanded biosimilars offering and the continued growth of Pfizer’s legacy brand emerging markets will help us to move the Established Pharmaceuticals business from a period of loss of exclusivity driven decline to potential growth. The Hospira acquisition was a clear growth driver and the integration continues to proceed well. We have addressed specific issues related to legacy Hospira’s manufacturing and have developed a plan to implement Pfizer quality standards at the sites and we have dedicated resources to support the site as they complete their transition with Pfizer network.

Based on Hospira’s excellent strategic fit with our established business and our intense focus on integration of Hospira, we expect to exceed our regional synergy targets of $800 million in annual cost savings by 2018 and now expect to achieve approximately $1 billion in cost savings.

As you are aware in early April we decided not to move forward with the Allergan transaction due to the actions of the US Treasury Department. Given these actions and the current political climate, we do not see any potential for a transaction involving inversions in the near term. While the outcome was disappointing, we always view the potential Allergan transaction not as a new strategy but were always a way to accelerate our existing strategy which remained unchanged. Our strategy is anchored by several elements namely improving the company’s revenue growth profile, the greater the portion of earnings per share growth is driven by incremental revenue opportunities.

Our latest product launches including Eliquis, Xalkori, Xeljanz, Ibrance, and Prevenar13 Adult have now become meaningful revenue contributors. In addition, the FDA’s decision to approve Celltrion’s biosimilar Infliximab across all eligible indications marks a critical and positive step forward in helping to create a pathway to biosimilars in the US. We hold the exclusive commercialization rights to this product in the US. While launch timing of Inflectra will ultimately depend upon a number of factors such as market place dynamics and intellectual property considerations.

We are continuing with the preparation of our launch plans for 2016.

Our current biosimilars portfolio includes three commercialized products available in select markets outside the US. Inflectra, Nivestim, and Retacrit. We believe that biosimilars represent an attractive revenue growth opportunity and for expand -- access important treatments. We also see continued opportunities for Established Pharm business in emerging markets with a robust portfolio positioned to compete in these markets.

GAAP revenues in emerging markets increased 10% operationally this quarter and company-wide revenues in emerging markets increased 14% operationally. Emerging markets revenues represented nearly 20% of our total company’s revenue.

We are also continuing to make significant progress in securing potential future growth drivers across the advancement for our pipeline. Specific examples include the plan submissions for ulcerative colitis for Xeljanz which is on track to occur in the first half of 2017. The acceptance to review of the Xeljanz EU filing for --- .

We have completed enrolment in the bococizumab SPIRE-2 outcomes trail. While it can be hard to predict duration of trial of the time to event trial, we currently anticipate a potential completion of this outcome study in the second half of 2017, presentation of the Phase 3 data at the American Diabetes Association meeting in June and a potential regulatory filing in the US. The Inotuzumab Phase 3 program where we are now conducting trials of osteoporitis, chronic low back pain and cancer pain indications.

A potential regulatory decision in the EU for Ibrance in combination with endocrine therapy for the treatment of HR positive HER2 negative advancement of the breast cancer and for Intuzumab for adult patients for relapsed or refractory positive acute lymphoblastic leukemia. We are in discussions with the FDA on our next steps to bring this important medicine to patients.

Behind these assets is a strong and early mid stage pipeline most notably a broad portfolio of compound which continue to advance. Our avelumab PD-L1 program with Merck KGaA has ramped up rapidly and now has 30 programs ongoing both as monotherapy in combination with other portfolio assets 8 of which are potentially registration enabling. We continue to expect that the key advances will come from novel combinations both double and triple combination regimes and technologies that may have the potential to treat more patients -- transformed the cancer treatment paradigm. We have several combination studies that are already in the clinic with our key combination assets being -- we also have the range of neurooncology assets moving into the clinic including our allergenic CAR-T program in collaboration with Cellectis and a small molecule immunotherapy asset idle one in collaboration with -- and our body specific antibody P --.

Recently we presented Phase 2 data at the AACR annual meeting sharing that -- is affective was effective in slowing the multiplication of cancer cells in patients diagnosed with early stage breast cancer who received no -- and we also expect that proof of concept we had with our next generation ALK inhibitor Lorlatinib and ALK positive non small cell lung cancer patients towards the end of the year. Lorlatinib is our respirational follow on drug to Xalkori.

In neuroscience we began Phase 2 proof of concept study this quarter for our novel dopamine modulation asset for Parkinson’s Disease. If successful this may have the potential to replace the standard of care in Parkinson’s.

In addition through a collaboration with MedGenesis Therapeutics, we have a second compound being investigated in Parkinson’s and expect to have a proof of concept study read out in the second half of the year. The compound is a GDNA protein and may have the potential to provide the first disease modifying treatment that slows the progressive decline in Parkinson’s.

We expect to have a proof of concept readout towards end of the year. -- growing hard to treat infection in the hospital and a long term care sitting. Currently there are no vaccines available to prevent the disease and the infection control practices are challenging to implement.

Overall we are anticipating a steady stream of pipeline updates throughout 2016. Our strategy will also capitalize opportunities in specific expertise resulting from our distinct competitive and growing businesses namely our Innovative and Established business. Each is led by strong leaders with the experience and know how to effectively direct and grow these organizations.

In addition to capitalizing on the strength of our pipeline, our strategy includes allocating our capital to shareholder initiatives with sustainable value creation. This includes continuing to look for ways other than inversions to improve our tax rate. It also includes the pursuing business development opportunities that use our capital efficiently in create meaningful shareholder value. I have the potential the near term solid value creation.

That strengthen our individual businesses and key assets and enhance our leadership position in the most attractive core areas as you know our decision framework has not change it continuous to based on these four questions. Are the business performing well within in Pfizer, could the business performed well as standalone entities, is the trade value in the combined entity and can trade value to be unlocked efficiently.

Throughout the year we will be assessing our performance into each of these factors. In summary the business is performing well -- strategy as I look for the year strong based on demonstrated ability the innovative and established businesses to executing this goal. We have a healthy pipeline with strong candidates at every stage of the pipeline and we have the financial flexibility and several options to creating short term and long term value for shareholders.

I will now turn over to Frank. Thank you.

 

Frank D’Amelio:Executive Vice President, Business Operations and Chief Financial Officer:

Thanks Ian good day everyone. As always the charts I am reviewing today are included in our webcast as a reminder because we completed the acquisition of Hospira in September the 3rd 2015. Pfizer’s first quarter 2016 financial results include three months of legacy Hospira global operations compared to first quarter 2015 results which do not include any legacy Hospira operations.

Now moving on to the financials. We had a good quarter, first quarter 2016, reported revenues were approximately $13 billion and reflect year-over-year operational growth of $2.9 billion or 26% of which $1.2 billion or 11% is attributable to the inclusion of legacy Hospira operations and approximately $900 million or 8% is attributable to five additional selling days in the US and four additional selling days in international markets in the first quarter versus the year-ago quarter.

Excluding Legacy Hospira operations in these additional selling days, reported revenue grew $800 million or 7% operationally which reflects continued strong performance of Ibrance, Prevnar 13, Eliquis, Xeljanz, Lyrica, and Chantix and a 14% operational growth in emerging markets which were partially offset by the absorption of approximately $300 million negative operational impact due to product losses of exclusivity. With respect to selling days I want to point out that because of our accounting calendar there was greater variability of selling days during the course in ‘15 then that will be in 2016. But this will not impact total number of selling days or our revenue for 2016.

Illustrate there were five more US and four more international selling days in the first quarter of ‘16 compared with the year-ago quarter and there are four few of US and three fewer international selling days in the fourth quarter of ‘16 versus the fourth quarter 2015.

So the imbalances to saw in the first quarter will be offset in fourth quarter 2016 and it will be essentially the same number of selling days in full year ‘16 as in full year 2015. Consequently the only impact will be to the quarterly year-over-year comparisons notably for the first and fourth quarters. Reported revenues continue to be unfavorably impacted by foreign exchange of $729 million or 7% including most as related to the Venezuela and Bolivar.

First quarter adjusted diluted EPS was $0.67 versus $0.51 in the year ago quarter increase was primarily due to increased revenues inclusion of Hospira operations, a lower effective tax rate and fewer diluted weighted average shares outstanding which declined by 78 million shares versus the year-ago quarter due to our share repurchase program which includes the impact of our 5 billion accelerated share repurchase agreement executed in February of 2015 and completed in July ‘15 and buy another 136 million shares associated with a partial quarter benefit in accelerated share repurchase agreement executed in March of 2016. Which will partially offset by an aggregate operational increase and adjusted cost of sales adjusted SI&A expenses and adjusted R&D expenses of $1.1 billion or 16%.

$0.07 negative impact due to foreign exchange and continuing product losses of exclusivity. Reported diluted EPS was $0.49 compared with $0.38 in the year-ago quarter due to the previously mentioned factors and the favorable impact of lower charges for business and legal entity alignment activities incurred during the first quarter which were partially offset by higher acquisition related cost, legal charges, purchase accounting adjustments and higher asset impairment charges.

Foreign exchange negatively impacted first quarter reported revenues by approximately $729 million or 7% and positively impacted adjustment adjusted cost of sales adjusted SI&A expenses and adjusted R&D expenses in the aggregate by $197 million or 3%. As a result foreign exchange negatively impacted first quarter adjusted diluted EPS by approximately $0.07 compared with the year-ago quarter. The results for the gift walk and get businesses are available and can be found at the end of the presentation that is posted on our website.

Moving on to our 2016 financial guidance, we are updating our 2016 reported revenues and adjusted diluted EPS ranges due to our strong performance to date and improved business outlook for 2016 as well as the favorable impact from foreign exchange rates since mid January 2016.

Consequently, we raised the midpoint our 2016 revenue guidance by $2 billion and then midpoint of our 2016 adjusted diluted EPS guidance range by $0.18. We now expect 2016 reported revenues to be in the range of $51 billion to $53 billion versus our previous expectations of $49 billion to $51 billion expect adjusted diluted EPS to be in the range of 238, 248 versus our previous expectation of 220 to 230.

I want to punctuate what Ian said previously. Operational factors such as our strong performance to-date 2016 in addition to our improved business outlook for 2016, favorably impacted the midpoint of the reported revenue guidance range by approximately $1 billion and the adjusted diluted EPS guidance range by $0.12

Favorable changes in foreign exchange rates since mid January 2016, also favorably impacted the midpoint of reported revenue guidance range by approximately $1 billion and the adjusted diluted EPS guidance range by $0.06. Finally given our first quarter results and the benefit of continued support of recently launched products as well as foreign exchange, we are raising the midpoint of our adjusted SI&A guidance range by $500 million . Consequently we now expect adjusted SI&A expenses to be in the range of $13.7 to $14.7 billion.

Key takeaways, this quarter marks our sixth consecutive quarter of Pfizer standalone operational revenue growth which was primarily driven by new products that are early in their life cycles such as Ibrance, Prevenar 13, Eliquis, Xelianz, Lyrica and additional selling days during the first quarter. As I just mentioned we raised the midpoint of our 2016 reported revenues and adjusted diluted EPS guidance range to reflect strong operational performance to date. Favorable changes in foreign exchange rates and improved business outlooks for 2016 we accomplished several key R&D milestones during the first quarter, we continue to deliver significant value to shareholders in the form of $1.9 billion first quarter 2016 dividend and $5 billion accelerated share repurchase agreement executed in March 2016 and finally we remain committed to delivering attractive shareholder returns 2016 and beyond.

With that I’ll turn it back Charles.

 

Charles E. Triano:

Thank you Ian and thanks for the prepared comments. Operator can we please move to the question-and-answer session.

 

Question-and-Answer

 

 

Operator:

Thank you ladies and gentlemen if you would like to ask a question please press star and the number one on your telephone keypad. Your first question comes from Greg Gilbert from Deutsche Bank.

 

Gregg Gilbert: Deutsche Bank:

Thanks clarification first question first the clarification Frank just wanted to confirm that the guidance increase to the full year nothing to do with selling days and then my question for John when is the earliest -- to be launched when you consider the legal and regulatory framework that exist today and then for Ian I am curious to hear your thoughts on how the recent treasury moves in your subsequent actions effect the decision to split or not to split if we don’t see obvious trap value today based on your and this your separation assessment consider the domicile -- other companies that could potentially maximize value for Pfizer shareholders. Thanks.

 

Frank D’Amelio :

So on the guidance, the guidance increased has nothing to do with the selling days, think about at this way, selling days in 2016 haven’t changed since we issued our initial 2016 guidance on the last earnings call. So short answer is absolutely nothing to do with our improved guidance it’s really about the operational performance the strong operational performance to a lesser extend foreign exchange.

 

Charles E. Triano:

Please John.

 

John Young:

Okay, thanks the question Greg. So in regard to in -- launch timing will ultimately depend on a number of factors including market place conditions, payer dynamics expected timing for ---- products and intellectual property related consideration among others. Pursuing stipulation entered in recent core conference related to ongoing litigation between Hospira, --- Johnson. Hospira agreed not to sale in -- on the US prior to June 29, 2016 exploration of the ---- patterns.

We are moving ahead, with the preparation of our launch plans for 2016 as you heard in Ian comments and we can’t comment further beyond those points.

 

Ian Read:

So Greg the delay course by of the potential split cause by Eligan was just the structural work needed to be done to incorporate I mean that going away it put it back on our original time line as we continue to work on that as a standalone company. Now there are many factors will take into account and we want to split or not and one of them is of course the tax structure of the two companies if they are split and I think the treasury action and the governance willing this to act in this area will make us think deeply about where all the alternatives to let part of this company if possible have a different tax jurisdiction.

 

Charles E. Triano:

We move to the next question please.

 

Operator:

Our next question comes from the line of Marc Goodman from UBS Securities.

 

Marc Goodman:UBS Securities:

Yes. Good morning just to continue on that process. Do you feel like you need to strengthen the innovative business before you would break this company up or you pretty satisfied what the way it is right now and if you split up can you give us your best estimate of what the disynergies would be and secondly just you mentioned on Prevenar there were government purchases can you quantify how much that helped in the quarter. Thanks.

 

Ian Read:

So, Marc the definitives can we do that first.

 

Charles E. Triano:

I can do the synergies. So Marc on the synergies once again assuming we work to our exercise or option and no decision has been made to date. The immaterial relative to overall earnings coupled current estimates are a couple of cents a share on an annualized basis.

And obviously we will fine tune that as we go forward but current estimates are couple of cents a share.

 

Marc Goodman:UBS Securities:

Prevenar

 

Ian Read:

Yes from Prevenar in the there was some U.S. There was some U.S. doing partner from this quarter it’s to a range of 40 millions approximately.

 

Marc Goodman:

Okay and on the businesses I think are strong enough to be standalone businesses to that have any further BD but either as separate companies or as one company we will always continue to look at during BD when it’s appropriate and when it can add value and that would be an ongoing process either pre or post split I would imagine from both companies perspectives. But always with a focus strong focus on value . Great thank you. We move to the next question please operator.

 

Operator:

Your next question comes from Steve Scala from Cowen.

 

Steve Scala: Cowen:

Good morning. I have two questions first Ian I have a follow up on an earlier question and I apologize for being picking but the fourth criteria for split appears to have changed a bit so previously it was kind of split done in a tax efficient way and today I believe you said kind of split be done in a efficient way so there were tax may have been diluted this is an accurate observation the interpretion of

 

Ian Read:

Probably get simplifying the cementics efficient means efficient both operationally and from a tax perspective.

 

Steve Scala:

Okay second question for Dr. Dale -- it would appear that Pfizer is in the first wave of IO combos, now considering that Pfizer one study ---- how big a disadvantage is it to Pfizer that you don’t have access to -- do you see -- will Pfizer’s other targets make for obsolete in your opinion. Thank you.

 

Ian Read:

Thank you for comment. I think -- was the first of the immuno quality of product but as you know its utility has been somewhat limited for both melanoma combo and combos because of its systemic immune activation which can be quite demanding for oncologies to manage although I am sure that there will be growing knowledge how to use the products we are much more excited about the new checkpoint augmenting compound like and that seems of our ability to augment different spots of the immune system on top of likely PD1 and PDL1 but we’ve retaining really promising tolerability so we seeing that’s the past to go compound that augment PD1 PDL1 but retain the favorable tolerability and that’s really our focus and really --

 

Charles E. Triano:

Thanks Michael, next question please.

 

Operator:

Your next question comes from Jami Rubin from Goldman Sachs.

 

Jami Rubin: Goldman Sachs:

Hi it’s -- for Jami Rubin thanks for taking the question. Just with regard to the GAAP business and the four criteria that you gave to determine whether or not to separate to GEP business, can you give us an idea what sort of metrics you plan to use to measure the performance of GAAP within Pfizer and the potential performance outside of Pfizer and then similarly what kind of metrics will you use to determine how much trapped value there is within GAAP and how efficiently that could be untrapped. Thank you.

 

Ian Read:

Thank you the metrics will inside Pfizer will be of course are they growth in their operations against budget as -- it will try and established -- like companies is would be easier for the innovative business it’s not as easy through the established because really the established business is a unique business including strong sterile injectable strong bus and the capabilities in big energy market and is not really generic business so it’s very hard to find a comparison there that we will I am sure we will declined some composite. On where we can unleashed with this trap value obviously you -- advisors but one of the classic methods would simply be look at some of parts. There is much as we can establish by disaggregating our business in same way as we give you information to do so we can take those businesses and compare in the standalone businesses and see what our potential evaluation would be over the past and compare to the sum. That is one way of looking at the trapped value another is to look historically what has happened the company where they spun or they have been spun in an unforced manner because of Managements decision and not because of active this pressure and see what has happened to the shares of those companies subsequently.

And of course we will set to look at the tax implications which really circles back to standalone abilities if company’s disadvantaged in a more specific way because the tax situation compared to their competitors.

 

Charles E. Triano:

Next question please.

 

Operator:

Your next question comes from Tim Anderson from Sanford C. Bernstein.

 

Tim Anderson:Sanford C. Bernstein & Company, Inc.:

Thank you a couple of questions please. My understanding is that before the Elegant they was terminated maybe a week before or something like that Pfizer went through around a lay of various folks kind of a mid management level and anticipation of the merger and obviously earlier in the two mono left. So now with deal offered I am wondering what the plan is from here in terms of filling these types of positions are you for example calling up -- we are going to leave -- for now I am trying to understand what sort of disruptions has might have caused unexpectedly.

And second question on splitting up how much for drive internally whether to do this my understanding is that because of different reasons there is an internal desire by lot of Pfizer for its kind of that mid manager level to kind of separate organization. I am not sure you have town hall meetings or that sort of thing. But what’s the feedback internally at the rank-and-file level on the company splitting up?

 

Ian Read:

Tim, so I’m really not aware of any layoffs or major changes prior to the Allergan deal. I think there were certain specific positions that may have been reorganized. But to answer your question succinctly, there is no disorganization or disruption. I think the results of the first quarter show that, so I’m not at all worried about that.

And as to the internal conversations, I would say they’re very robust. We have a great enterprise-wide view on the company that stems from John’s leadership in Established and his team. And the internal decisions or internal motivations are totally directed to what we believe would be best for shareholder value, and it’s a very transparent process. So I don’t think there are in any way factions within the company trying to push one way or the other.

We’re all focused as a management team on what the best decision for Pfizer shareholders would be. Thank you.

 

Charles E. Triano:

Thanks, Ian. Next question, please?

 

Operator:

Your next question comes from Chris Schott from JPMorgan.

 

Christopher Schott: JPMorgan Securities LL

Great, thanks for the question. I just had two on business development. I guess the first one is can you just elaborate on your priorities and appetite at this point? I guess as part of that, do you have a bias when it comes to bolstering Innovative versus Established? And is there a focus on in-market or near-to-market products versus pipeline?

The second question was about the competitive environment for business development. I know you’ve been very financially disciplined in the past, but it appears that we’ve got a pretty competitive environment out there, and some of your peers may be less focused on ROI than you are. How do you balance that opportunity to acquire attractive assets with maximizing long-term shareholder value in this environment? Thanks very much.

 

Ian Read:

Thank you. Our BD approach has always been one of BD is not a strategy. It complements our ongoing strategies. So I think our BD post-Allergan remains on that same course.

We’ll look for assets that we think can add value to shareholders that are appropriately priced and meet our returns. We’ve always been very disciplined on that, although not concerned about pulling the trigger when we see those opportunities.

So I think there is after all the work we’ve done on the Established side, there would be a tendency towards a bias to the Innovative side. And we would be biased I think more towards products that are near-market or in-market that we believe we could generate incremental growth and value by owning them rather than looking at very early products because we think we have a very full and complete pipeline in that area. On the competitive stance, I’d ask Frank to make a few comments on that.

 

Frank A. D’Amelio:

Sure. So I think, Chris, the way to think about this, at least the way we think about this, is clearly there has been some changes in valuation in sectors within the industry. So biotech, for example, clearly has had a change in valuation, a decrease in valuations.

Without speaking for those management teams or those boards, I think at a macro level, if you were to ask do they believe that their current valuations represent the valuations of the company, I’d say I’m not sure. I think that they’re probably in transition, that they really haven’t decided that that most of the latest valuations are indeed the valuations that are real valuations. What I always believe is what really will determine this are when those individual companies have to go out and have a capital market event. The capital market event will be very informing in terms of what the valuations of those companies are and so I think over time we’ll see some of that thinking take place.

 

Charles E. Triano:

Next question please.

 

Operator:

comes from John Boris from SunTrust.

 

John T. Boris: SunTrust Robinson Humphrey, Inc.:

Thanks for taking the questions and congrats on the results. So first question, just on Chantix, on the EAGLES results that you got, is that going to help to relax the need to mention neuropsychiatric side effects on direct-to-consumer advertising ads? And we’re already seeing a nice uptick, but if you’re able to relax that, one would think that you might be able to see a faster uptick.

Second question on GEP, you’ve indicated that you’re going to be divesting the pumps business. Where are you in the process on identifying a financial or strategic buyer for the pumps business and one of your competitors announced this morning that they’re going to spinning their hemophilia business. Any thoughts within the innovation core to possibly considering staying and/or divesting businesses that aren’t receiving enough R&D attention that could be better as standalone businesses out of Innovation core? Thanks.

 

Ian Read:

Okay. Albert, if you could, talk about Chantix, please.

 

Albert Bourla:

Yes, obviously, I’m very pleased with the positive results of EAGLES. In this monumental study, the authors concluded, as Ian said, that the trial did not see a significant increase of first year’s neuropsychiatric adverse events with Chantix or bupropion compared to placebo and nicotine patch. We are submitting this data to various regulatory bodies, proposing revisions to the product labeling, including a request for the removal of a boxed warning. We believe that the available scientific evidence does not support the boxed warning, and to look forward to discussing this data with FDA, EMA, and other global regulatory parties.

 

Ian Read:

Thank you. I would just add that also having it published in The Lancet is clearly good medical communication and education and will allow an appropriate dialogue. John?

 

John Young:

Okay. So thanks for the question, John. So maybe I just wanted to correct any misunderstanding that may be out there because we’ve made no announcement regarding any intention to do anything in regard to our pump or Infusion Systems business. We’re obviously aware of market speculation, which we don’t comment on.

Across all of our businesses, we regularly review our business portfolio from the perspective of maximizing value creation. If there are any developments with our business, we would certainly communicate that publicly. But as I think as we’ve said previously, we believe that in the Hospira acquisition we acquired what is a scarce asset that is performing well. The management team have taken the right steps to turn the business around, and we are extremely positive about the opportunity to continue to help the Infusion Systems business to perform well and to return to growth.

 

Ian Read:

Thank you. And, Frank, if you could, talk about the...

 

Frank A. D’Amelio:

Hemophilia?

 

Ian Read:

Hemophilia, I think it was hemophilia.

 

Frank A. D’Amelio:

Yes, so obviously, John, we’re aware of the announcement this morning on the hemophilia business of one of our competitors. The way I think about this is we’ve done similar things in the past. If think about our sale of Capsugel, the sale of Nutri , the creation of Zoetis, I think our compass on all those transactions has been creating shareholder value.

Our compass going forward will continue to be creating shareholder value. If we think there’s an opportunity to do that through any action, including something like a spin, we would clearly consider it. Hopefully, our actions in the past have demonstrated that we have more than a willingness to do that.

 

Charles E. Triano:

Thank you Frank. Next question please.

 

Operator:

Your next question comes from Seamus Fernandez from Leerink.

 

Seamus Fernandez:

Hello, thanks very much for the question, so I just had a couple here. First off, can you talk a little bit about the expectations for biosimilar product launches outside the U.S. and how you see them evolving relative do Inflectra’s launch, which seems to have been ahead of expectations?

The second question is relative to international Enbrel. Is Inflectra uptake and Remicade pricing a good comparison for Enbrel’s performance as biosimilars hit the market in the next call it eight to 12 months?

And then the last question is on consumer. On the recent GlaxoSmithKline conference call, when asked about interest in additional consumer assets and the possibility of interest in Pfizer’s consumer business, the current CEO suggested that they continue to evaluate all options and would welcome opportunities to participate in these larger assets. I guess my question is how creative are you willing to get with the consumer business in order - and would a ViiV-like deal be ever a consideration for the consumer business at Pfizer? Thanks.

 

Ian Read:

So thank you, Seamus. I’ll deal with the consumer one first. Look, the consumer asset in Pfizer’s portfolio is a very valuable asset. It’s growing well.

We’re continuing to add to that business. We have a great management team. That being said, all of Pfizer is aware internally that we continually look at all of our different assets, and we’re always focused on creating shareholder value. To this date or to this moment, I think the best way of creating shareholder value is the plan we have with consumer growing inside Pfizer.

As facts change, we’re always willing to look at those facts. If you could, deal with the biosimilars, John, please.

 

John Young:

Yes, so thanks for the question, Seamus. So clearly, biosimilars are a very important part of the GEP growth strategy. The portfolio consists of both Pfizer, legacy Pfizer and legacy Hospira assets as well as some assets from external partnerships. Per your question, we remain very bullish about the opportunity.

There’s something on the order of $100 billion of currently patented branded biologics expected to lose patent protection in the next five to 10 years. And the global market for biosimilars is expected to grow from around $1 billion annually in 2013 to somewhere on the order of $17 billion to $20 billion in 2020.

In regard to our plans for our portfolio, we have overall around nine distinct biosimilar molecules in different stages of development and approval. We’re going to look to optimize the launch of that portfolio on a global basis over the coming years.

 

Ian Read:

Albert, could you discuss the impact on Enbrel?

 

Albert Bourla:

Yes, first of all on the pricing, let me say that I don’t think we can draw conclusions from one biosimilar to the other. Everyone has its own dynamic. From the limited pricing for Enbrel biosimilar so far, the discount levels are in line with our expectations, and we expect Enbrel’s pricing to be competitive.

Now in a general comment on the performance of biosimilars, so far Enbrel had a strong quarter of 8% up, so basically no impact to date from biosimilars, but of course it’s very early. We do expect a modest uptake of biosimilars. But due to their limited long-term safety and efficacy data, at launch we anticipate their use will be primarily in new patients.

 

Ian Read:

Thank you, Albert.

 

Charles E. Triano:

Our next question, please?

 

Operator:

Your next question comes from Mark Schoenebaum from Evercore ISI.

 

Mark J. Schoenebaum: Evercore ISI:

Hey, guys. Thanks for taking the question. Hey, Ian, I appreciate your comments regarding you’ll make a decision on a potential split-up by the end of 2016.

Can you confirm or not confirm that decision would be a yes or no that you would split by the end of 2017, or should we be extending our timeline for the actual timing of a split?

And then number two, I know you’ve given this before, Frank. But can you just comment roughly speaking on what you see the go-forward growth rates for both the growth business and the Established Products business mean? I think you’ve given us a ballpark figure for that. I know there’s no official guidance out there. But just a ballpark figure, it would be nice to get those ballparks refreshed.

And then finally, you had made some commentary, Frank, around - I think you had made some commentary around the leverage ratio that the Allergan Pfizer NewCo, you’d be willing to take the Allergan Pfizer NewCo to. I was just wondering. Now that obviously Allergan isn’t going to be part of the future, what kind of leverage ratio you guys would go to, to maximum and whether or not you would be willing to take out debt in order to do a large share repurchase? Thanks a lot.

 

Ian Read:

So on the timing of the split, if we made a decision to split in the fourth quarter, we believe that the transaction could be completed by the end of 2017. Obviously, those timelines are subject to change if we encounter things that we don’t expect in the process. But right now, the planning assumption would be with a fourth quarter decision, we would be able to complete the transaction by the end of 2017. Frank, do you want to handle the other question?

 

Frank A. D’Amelio:

Sure. So on the going-forward growth rates, I haven’t provided going-forward growth rates other than our 2016 guidance for revenue, which we just increased by $2 billion, $1 billion of which was operational.

On the leverage ratio, what I’ve said previously, Mark, on that is I’d be willing to take it to 2.5 to three times. We mentioned that as part of when we’ve gone through some of the Allergan meetings. So by the way, if I was willing to do it for that, I’d be willing to do it for the right transaction on a going-forward basis.

In terms of leveraging the balance sheet for buybacks, the way I think about this is if you go back to 2010, and if you include the $5 billion accelerated share repurchase that we added this past March, $50.7 billion of share buybacks, $50.7 billion, 1.9 billion shares excluding the 405 million shares as a result of the Zoetis exchange. So we’ve done actually a massive buyback without having to borrow or leverage the balance sheet, which allows us to keep our powder dry if we wanted to do a different kind of transaction.

So hopefully that answers your question.

 

Charles E. Triano:

Thanks, Frank. Operator, can we move on to the next question?

 

Operator:

Your next question comes from David Risinger from Morgan Stanley.

 

David R. Risinger: Morgan Stanley & Co. LL

 

Thanks very much. With respect to considerations for Established Products, could you just comment on how you’re considering potentially shifting Viagra and Lyrica from the Innovative segment to Established Products?

Second, could you just discuss your plans to launch a biosimilar Remicade in the U.S. this fall and your level of conviction there?

And then third, could you help us understand how we should think about Prevnar comps going into next winter? Obviously, Prevnar has been extremely strong, but that may present tough comps a year from now. So any color on your thinking there would be helpful. Thank you.

 

Ian Read:

Yes, so we would expect that we will continue with our policy to move products like Viagra and Lyrica as they get close to be peri-LOEs from one business to the other. The exact timing we would decide. But in general, you clearly want to have an Innovative company that is focused on growth and not focused on managing the end cycles of products like Lyrica and Viagra.

On the biosimilar Remicade, I really think John has made comments on that, and we really can’t add any more than that. I wouldn’t say that we are preparing for a 2016 launch, and it’s dependent upon the factors that John has already mentioned. And, Albert, on the Prevnar comps.

 

Albert Bourla:

Yes, let’s start at the top. In the U.S., we said we had operational growth of 28%. So apparently, we continue to do an excellent job with a catch-up opportunity. But to put it into context, as of the end of the quarter, from the 49 million adults eligible for vaccination, we have already covered 37% of them.

In fact, the vast majority previously vaccinated was new ones As we have said before, while many adults remain, this cohort is much more difficult to capture. And going forward, we expect the U.S. adult revenues to decline compared to last year. These will be partially offset by Europe and the rest of the world, which achieved 63% operational growth this quarter and will continue growing strongly.

And also, as both Ian and Frank said in the beginning, the adopting pediatric will have a strong performance. So as a whole, the Prevnar franchise will have very comparable revenues this year compared to last year.

 

Charles E. Triano:

Thanks, Albert. Next question, please?

 

Operator:

Your next question comes from Vamil Divan from Credit Suisse.

 

Vamil K. Divan :Credit Suisse:

Hi, good morning. Thank so much for taking my questions. So two on the immuno-oncology side, so one just on avelumab.

I believe Merkel cell you mentioned as the lead registrational indication there. I’m wondering if you have that data in-house now. And are you still confident in getting that filed an accelerated manner? And if you could just clarify, between yourselves and Merck KGaA, how the registration process works, who’s in charge of that, or is it done jointly?

And then second on the combination side, you mentioned 4-1BB and OX-40 being two of the key agents as you think about combinations. Can you just talk a little bit about how you prioritize those two, given it seems like several companies have OX-40s in early development, while 4-1BB it appears it’s just you and maybe one or two other competitors? I’m trying to get a sense of how important having something that is unique or differentiated to offer physicians and payers for combinations could be going forward when you think about how to prioritize resources behind the two different agents. Thank you.

 

Ian Read:

Okay. I’ll ask Albert to talk about the Merkel cell and the registration split of responsibilities. And then Mikael can deal with the choices we make between our unique 4-1BB and our OX-40.

 

Albert Bourla:

Yes, with regards to Merkel cell, first of all we are going to have some data presented at ASCO this year. It will be an oral presentation. We have already received Breakthrough designation, and we plan to file this year. The work between us and Merck KGaA is split in a very collaborative way.

They are doing parts of the work and we are doing other parts, and we have very good collaboration. So we are very confident on executing on that.

 

Ian Read:

Mikael?

 

Mikael Dolsten:

Yes, so both our 4-1BB and OX-40 have unique design versus major competitors and as you know, our 4-1BB has performed very well when it comes to tolerability and we already reported last ASCO of augmenting effect when combined with rituximab, and we’ll start reporting early signs when combined with PD-1 and PD-L1 this year. So we do think that 4-1BB will be a key molecule as the performance we start to see. We are the only company that can put a 4-1BB/OX-40/PD-L1 in place, and we’re moving swiftly to have that as an option and expect late this year or early next year to have that triple combo.

 

Ian Read:

Thank you, Mikael.

 

Charles E. Triano:

Thanks, and can we move to the next question, please?

 

Operator:

Your next question comes from Colin Bristow from Bank of America.

 

Colin N. Bristow: Bank of America Merrill Lynch:

Good morning and thanks for taking the questions. On potential competition to Ibrance, there’s increasing optimism on the Street around Lilly’s CDK-4/6, and I guess we’ll see data on that at ASCO. Could you just discuss how you view Lilly’s and Novartis’s CDK-4/6 in terms of their level of threat to Ibrance going forward?

Second, on the Xeljanz filing in the EU, what’s your level of confidence that this will get through, and what you feel you satisfied in this submission that previously had been lacking?

And then lastly, just in your earlier-stage pipeline, any assets you would highlight that you’re particularly excited about that we should be paying closer attention to? Thanks.

Ian C. Read - Chairman & Chief Executive Officer

Okay. I think why don’t we ask Mikael to deal with the early assets that we’re excited about and perhaps also comment on the Xeljanz submission, and then Albert may want to add something. And then Albert will deal with the Ibrance competitive situation.

Mikael Dolsten - President-Worldwide Research & Development

Yes, thank you. So we have a very comprehensive pipeline. As you heard, Ian alluded to that in his prepared remarks. We have 85 projects spread across Phase 1 to Phase 3 registration.

And let me just mention a couple that we think will be really unique and differentiating. We already touched base on 4-1BB, on OX-40, and the triple I-O combo. Lorlatinib in the ALK and ROS space is generating very interesting data that we will start to share. We have a novel ADC called PTK-7 that we’ll also see some real interesting response rates.

In the immuno- inflammation field kinesis going into Phase 2, with several highly specific JAKs going to inflammatory bowel disease, dermatological inflammation, and lupus. So we will share more data around those, but I think that will really move the entire JAK field over time into new areas and with the new profiles.

Vaccines, it’s always CDs and stuff (57:40) obviously that we are really excited about. And Ian mentioned in his introduction that we have built some interesting assets in Parkinson’s with a completely novel dopamine modulator, and also have an interesting GDNF study together with MedGenesis.

And finally, in rare disease, I’ll exemplify that we have a growing sickle cell franchise with rivipansel and a plan to start PD-9 as a way to prevent occurrence of difficult-to-treat rare disease episodes. So you can see our opportunity spans multiple therapeutic areas.

Xeljanz in Europe I think is based on a very comprehensive file. We have six complete clinical trials with two open-label extensions. And all our program contains more than 19,000 patients here, more than 6,000 patients in long-term extension up to eight years. And please, I want to just to remind everyone that Xeljanz has been used by more than 6,500 physicians and more 50,000 patients in the U.S. with a very favorable profile.

So you can see it’s a completely different profile we have now with the European regulatory agencies and we also have some specific sub-studies that we’re interested on that we have executed on. So we view the dialogue with them as very constructive at this moment.

 

Ian Read:

Thank you.

 

Albert Bourla:

I have nothing to add in Xeljanz, just maybe that it is already approved in more than 45 countries. And let me move to Ibrance and competition. I cannot really speak much about competition, but it includes Lilly and Novartis because there is limited clinical data in the public domain on the efficacy and safety. What I can do is I can speak about our product, and I can tell you we have the most advanced and broad program in the industry.

Firstly, we are the only company with a registered product in the U.S. and eight other countries and an accepted filing in Europe where we may obtain registration this year. In just over a year in the market, Ibrance has been prescribed by almost 7,000 physicians and is up to more than 28,000 patients.

That these are up today is a testament to its efficacy and outstanding safety profile with a very low rate of global three and four GI effects such as fatigue and diarrhea. Ibrance has delivered positive results across three randomized pivotal trials. It’s been studied in an additional five pivotal studies in early, advanced, and recurrent breast cancer as well as 62 ongoing investigator-initiated research, 38 of which are in breast cancer and 28 are in non-breast cancer. So this is what I call a clear lead.

 

Ian C. Read:

Thank you, Albert.

 

Charles E. Triano:

Thanks, Albert. Next question, please?

 

Operator:

Your next question comes from Andrew Baum from Citi.

 

Andrew S. Baum: Citigroup Global Markets Ltd:

Three questions, please. First, Ian, you touched upon triple combinations, or it may have been Mikael. There’s obviously a significant cost burden attached with that. Could you talk to the idea of where you feel specialist care pricing is going in the U.S.

And how quickly is biosimilars’ cost effectiveness arguments in a gridlocked House sufficient to maintain the status quo, or how do you anticipate and how quickly do you anticipate change?

Second on PBMs, again to Ian, some of your peers have identified PBMs as bad actors in the whole healthcare value chain given their disproportionate rebate capture. Do you believe that PBMs or rather pricing transparency is a good or a bad thing from an industry perspective?

And then finally for Mikael, I saw some data recently on Selzentry, your CCR5 antagonist, in an immuno-oncology setting. Do you have any plans to develop that drug within that setting, or is the IP an issue? Thank you.

 

Ian Read:

So on the pricing oncology assets, clearly products are sold on their value and the value of the patients and those of society, but there is also an element of total affordability. So I think the ability of companies to have the complete regime like with Pfizer’s case the PD-L1, the OX-40, the 4-1BB, or a small molecule will enable offerings to payers that I think society will find acceptable from a cost/benefit return as distinct from looking at the complications of acquiring all those elements separately in the marketplace.

On pricing itself, I agree with you. There is a large amount of rhetoric given the election year. And there is concern from individuals about accessing pharmaceuticals. This is extremely complex.

It’s in great part due to the pressure on plans that have been transformed away from having the ability to really be an insurance company and become somewhat more of benefit administrators than insurers. It has to do with the quality of insurance and also to do with the value of these specialty products. So I expect a robust discussion. But I expect that in the end, the United States will continue to support innovation and find ways to make sure that innovation is supported and products get to patients.

And that will obviously be a robust policy discussion, but I do think in the end that’s where the United States will end up in that discussion.

On PBMs, in a market-based system, PBMs provide value by aggregating volumes and negotiating discounts. To the extent those discounts are passed on to the end user or the end payer or an appropriate amount is passed on and they’re serving a valid market function, as the market changes, they may have a larger or smaller role. But I think what I would emphasize is I like to see a marketplace work. I like to see incentives in the marketplace to ensure it works, and I like to see the appropriate amount of transparency.

So that’s really all I can really comment on that. Thank you.

 

Charles E. Triano:

Mikael is supposed to talk about Selzentry.

 

Ian Read:

Mikael, yes.

 

Mikael Dolsten:

I think you were likely referring to our CCR2 small molecule antagonist. And we have together with an academic collaborator really observed some interesting effects on suppressive immune cells in pancreatic cancer and some early encouraging clinical signals. So we do continue with a second study in pancreatic cancer with the CCR2. And in total, we currently have eight different new medical entities in the immuno-oncology field in the clinic, and expect by the end of this year to have 10 different immuno-oncology compounds in the clinic.

 

Ian Read:

Thank you.

 

Charles E. Triano:

Thanks, Mikael. Mickael. Next question, please?

 

Operator:

Your next question comes from the line of Geoff Meacham from Barclays.

 

Geoffrey Meacham: Barclays Capital, Inc.:

Good morning, guys. Thanks for taking the question, just a couple. Ian, can you continue the strategy discussion? I want to get a sense as to what at this point you’d characterize as the top one or two priorities post-Allergan and when you look at things like tax rate, cash flow, expected multiples, or growth rates.

And then just on the pipeline front, a few for Ibrance, the adjuvant trials really aren’t until much later, say 2020. But how do you see the role of CDK-4/6 in this, and does your long-term thinking assume success here? And then for bococizumab in PCSK9, clearly, outcomes data are going to dictate the share. But much of a role do you think that imaging plays through IVUS in product differentiation? Thanks.

 

Ian Read:

Thank you. The priorities post-Allergan continue to be our four strategies, which is to continue to show excellence in our Innovative core and bring forward Innovative products. I think you’ve seen us do that. Continue to drive the growth rates of our inline and newly launched products, which you can see are happening.

Eliquis is performing extremely well, with an LOE in the United States out I think in 2019 - sorry, Lyrica that is. Eliquis is doing very well. Xeljanz is doing well.

So I think the priorities are: continue to ensure that our science comes to market; grow our inline products, which I think we’re doing well; execute on capital discipline, which we continue to do; and in our Established Products businesses is to roll out successfully the biosimilar strategy, to continue to utilize and maximize the value of our sterile injectables around the world. So frankly, I think there is lots to do in that area.

We’ll continue to look at our tax situation. We have a very good tax group, and Frank and his team are very good at looking how to improve that. It continues to be an area of focus.

Vis-a-vis Ibrance, I agree with you that the trials are on the timelines you talk about, but that’s the nature of the trials in oncology. And the reality is we have already started those trials and are well ahead of any of our competition. So it’s a matter of a lead established in the marketplace. So I’m very optimistic about the long-term growth rates of Ibrance, both in the indications it has now and the indications to come as we go earlier in breast cancer.

And also outside of breast cancer I think we have a lot of work going on. And then you asked - the last question was?

 

Charles E. Triano:

Boco, PCSK9.

 

Ian Read:

Boco, I’ve always thought, and we discussed this, that boco, or these products should only have been launched when you have outcomes data. I’ve always felt, and I think if you go back in our transcripts, we’ve always said that on LDL alone, it will be difficult to convince society to pay what’s necessary, and you really need to include along with LDL in the outcomes. So clearly outcomes is important. Imaging has been used previously with lipid agents.

It doesn’t really move the needle. What moves the needle is the large prospective trials which show that outcomes are changed. And an image just doesn’t do the same as that data. So I look forward to that class expanding when we have the outcomes data and we have the right value equation for society.

 

Charles E. Triano:

Thank you, Ian. Next question please?

 

Operator:

Your next question comes from Manoj Garg from Healthco.

 

Manoj K. Garg: Investment Strategy LL

Hi, thanks for taking the questions, one for Albert on Ibrance and then just one for Frank on financials. When would you expect submitting PALOMA-2 data to FDA? And then maybe you can just talk about what that would do to the intent-to-treat population. And then just to follow up there, what is the general timing in Europe on approval?

And then for Frank, on the $500 million increase in SI&A, is that driven largely by FX, or is there some additional investment there?

 

Ian Read:

Go ahead, Albert, please.

 

Albert Bourla:

Thank you. As you know, we announced positive top line results from PALOMA-2. We will present details at ASCO with an oral presentation. It will be a late-breaker.

Now this trial provides additional confirmatory evidence on the benefits of Ibrance for breast cancer patients. So this will add to the momentum of this. Also, it will be used for regulatory filings. It is a requirement from FDA so that we can convert the accelerated approval to a permanent approval, and we plan to file.

We are in discussions now with the FDA.

In EU we have already filed. We have an accepted filing based on PALOMA-1 and PALOMA-3. But also we have submitted already PALOMA-2 over there as additional supporting data. And as we said before, we expect to receive Ibrance approval in the U.S. as early as this year if eventually...

 

Ian Read:

Europe.

 

Albert Bourla:

Excuse me, in Europe as early as this year if we have a positive opinion from European authorities.

 

Ian Read:

Thank you. Frank?

 

Frank A. D’Amelio:

And on the SI&A and the effect and the impact of FX, so we took it up $500 million. The midpoint went up $500 million. Approximately half of that is due to foreign exchange.

Approximately half of it is due to operations, including increased investment in new and certain inline products.

 

Charles E. Triano:

Thanks, Frank. Next question, please?

 

Operator:

Your next question comes from Richard Purkiss from Piper Jaffray.

 

Richard J. Purkiss: Piper Jaffray Ltd:

Thanks, guys. I’ve got three questions. Firstly for Albert, can you update us on your thoughts on how Prevnar penetration into the adult indication is likely to play out over the next 12 months in Europe? Secondly, also for Albert, can you give us an update on how well the adjuvant breast cancer studies are enrolling?

And then thirdly, perhaps for Mikael, also on Ibrance, whether you see it largely restricted to the ER-positive HER2-negative breast cancer setting, or whether its mechanism ultimately gets used for other metastatic tumors too? Thanks.

 

Ian Read:

Okay, Albert.

 

Albert Bourla:

Yes, let me start with Europe. As I said, in Europe we have 63% operational growth, and this will continue. We will have strong growing in Europe. The demographics are very favorable over there.

We have a larger eligible population. But the price per dose is less than in the U.S. And also another factor is that we need to obtain a recommendation. And this is a process that in Europe can take - recommendation and reinvestment - can be phased over two years because it’s happening country by country.

In some cases, within the same country it’s happening district by district. So we are working very, very intensively on that because we see the opportunity as a major one.

But moving to how we are doing with our expansion into other breast cancer segments and particularly into the adjuvant setting actually, we have two studies in the adjuvant setting. That’s PENELOPE-B. This is for high-risk early breast cancer, and we have PALLAS for intermediate-risk early breast cancer. And they are recruiting very nicely right now. I need to also emphasize that we have another one which is in pilot.

It is a collaborative study, but it is in the neo-adjuvant setting with collaboration with the Washington University.

 

Ian Read:

Thank you. Mikael?

 

Mikael Dolsten:

So we are increasingly excited as we have learned more about Ibrance how significant we can see opportunity to expand utility or potential of that drug. So we have studies ongoing, and we will likely see some data this year or next year in head and neck cancer in combination with Erbitux Pfizer-sponsored and collaborative studies, in Mantle cell lymphoma with ibrutinib, and in pancreatic cancer in combination with abraxane in 2017. And more recently, we’re also studying EGFR mutant lung cancer combining Ibrance with our own PF7775 EGFR inhibitor.

Also within breast cancer, we see opportunities and have initiated triple therapy based on Ibrance, as well as we’re looking at the novel segment of breast cancer that may go from ER into double-positive segments. So substantial opportunities and of course our antigen is growing as we see how well Ibrance is performing. The patient experience is so good and our confirmatory studies deliver real encouraging data.

 

Ian Read:

Thank you, Mikael.

 

Charles E. Triano:

Next question, please?

 

Operator:

Your next question comes from Alex Arfaei from BMO Capital Markets.

 

Alex Arfaei: BMO Capital Markets:

Good morning, folks. Thanks for taking the questions and congratulations on the quarter, three questions, if I may. Ian, on business development, all things being equal, would you prefer ex-U.S. Assets so that you can deploy your capital more efficiently? Second, apologies if I missed this, but can you tell us what Prevnar Adult sales were by in the quarter by U.S., ex-U.S. if possible? And then finally on the Hospira business, it was a little bit lower than we expected despite the higher selling days.

Could you comment on that, and is it because your own sterile injectable business is doing better? Thank you.

 

Ian Read:

Thank you. On the question of U.S. or non-U.S., as I said, we’re value investors, so it comes down to what is the return on assets and what’s the NPV. And of course, in that would be included the different costs of doing either an onshore or offshore deal.

So we would make that decision based on that. Next, I think it’s Mikael. Sorry, Albert?

 

Albert Bourla:

Yes, Prevnar Adult global sales were $439 million, so that was 31% of that. But most of that was in the U.S., $390 million were in U.S. and $47 million were internationally. International, as I said, grew 63%.

 

Ian Read:

Thank you. And the last question

 

John Young:

Was global Hospira sales?

 

Ian Read:

Yes.

 

John Young:

So overall we’re very positive about the performance of the Hospira business. We saw positive performance across all of our segments this quarter with sterile injectables, biosimilars, and the infusion system. This business continues to return to growth overall. In addition, with the ongoing efforts to integrate the two companies that are ongoing but proceeding very well and in line with our plans, we remain very positive about the performance that we’re seeing from the legacy Hospira business.

 

Frank A. D’Amelio:

And we increased our synergy target from $800 million to $1 billion.

 

Ian Read:

Thank you, Frank, for the add.

 

Charles E. Triano:

Thanks. Can we take our last question, please?

 

Operator:

Your final question comes from Jeff Holford from Jefferies.

 

Jeffrey Holford: Jefferies LL

Hi, thanks for taking my question. Just first off, can you help us think about the potential investor positioning the GEP to help us think about valuations, you say there aren’t good comps out there, but I would tend to think of this as perhaps a slower growing part of the business but perhaps one that could sustain a greater dividend than the rest of the business over time. So just help us think. Is that the investor positioning of that business?

Secondly, on Ibrance, I wonder if you could just on the basis for the U.S. What’s the duration of therapy that you’re seeing and what’s the market share in the unlabeled population? And then just last question, have you prioritized any specific tumor types or indications yet for either 4-1BB or OX-40 in terms of pivotal planning? Thank you.

 

Ian Read:

Okay. On GEP, I’ve always used the analogy that it’s like the pharmaceutical business that really given it’s in sterile injectables to sell on quality and barriers to entry; and given its biosimilars which also will be eventually sold on the quality of the manufacturer and the data we have. And then the emerging markets, which is sold on brands and quality that it looks like a consumer business with just a touch more risk than a normal consumer business, so perhaps some nice comparables. The P/Es really ought to be the consumer-like business.

Now you may or may not agree with that, but it’s slower growing, growing with GDP just like consumer businesses do, being sold on brands, and then a little more affected because it does have pricing risks and some development risks. That’s how I would look at it. Ibrance?

 

Albert Bourla:

Yes, the first-line market there is now 38%. That’s number one. We have achieved and have surpassed AI monotherapy. The second and third-line markets there are 26% and 14% respectively.

But when it comes to duration of treatment, it’s too early to assess because as you know, the product has been launched a year approximately ago, and PFS duration from the data it is around 20 months since PALOMA-2. So still we need some time to assess what would be the actual progression-free.

 

Ian Read:

Thank you.

 

Mikael Dolsten:

Yes. So on one hand with 4-1BB, we presented last year at ASCO and we will provide update during this year, 4-1BB with rituximab being lymphoma that had very promising response rate in refractory with rituximab patients about 35%. We have expanded that study. It looks certainly very promising.

So that could be one opportunity for moving 4-1BB fast forward. 4-1BB and OX-40 are expressed in many tumors in the immune infiltrating cells. So we will have a broad ambitious program where we see opportunity for these across many different solid tumors and some blood related cancers.

 

Ian Read:

Thank you, Mikael.

 

Albert Bourla:

Let me make a correction. I think I said 20 months in PALOMA-2. It is 20 months in PALOMA-1. We haven’t disclosed the duration treatment of PALOMA-2.

We’ll do that at ASCO.

 

Charles E. Triano:

Right. Thank you, Albert, and thank you, everybody, for your attention today.

 

Frank A. D’Amelio:

So long, everybody.

 

Ian Read:

Thank you.

 

Operator:

Ladies and gentlemen, this does conclude Pfizer’s first quarter 2016 earnings conference call. Thank you for participating. You may now disconnect.

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Posted In: EarningsNews
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