Good day, ladies and gentlemen and welcome to the Fourth Quarter 2011 Emergent BioSolutions Earnings Conference Call. My name is Jeremy and I will be your operator for today. At this time, all participants are in listen-only mode. Later we will conduct a question-and-answer session. I would now like to turn the conference over to your host for today, Mr. Bob Burrows, Vice President of Investor Relations.

Thank you, Jeremy. Good afternoon, ladies and gentlemen, thank you for joining us today as we discuss Emergent BioSolutions fourth quarter and full-year 2011 financial results. As is customary, our call today is open to all participants. In addition, the call is being recorded and is copyrighted by Emergent BioSolutions. Joining me on the call this afternoon with prepared comments will be Fuad El-Hibri, our Chairman and Chief Executive Officer, and Don Elsey, our Chief Financial Officer. Additional members of our senior management team will be present on the call for purposes of the Q&A session. Before we begin, I am compelled to remind everyone that during the call management may make projections and other forward-looking statements regarding future events and the company’s prospects or future performance. These forward-looking statements reflect Emergent’s current perspective on existing trends and information. Any such forward-looking statements are not guarantees of future performance and involve potential risks and uncertainties. Actual results may differ materially from those projected in any forward-looking statements. You’re encouraged to review Emergent’s filings with the SEC on forms 10-K, 10-Q and 8-K for more information on the risks and uncertainties that could cause actual results to differ. For the benefit of those who may be listening to the replay, this call is held and recorded on March 8, 2012. Since then, Emergent may have made announcements relating to topics discussed during today’s call. So again, please refer to our most recent press releases and SEC filings. Emergent BioSolutions assumes no obligation to update the information in today’s press release or as presented on this call except as may be required by applicable laws or regulations. Today’s press release may be found on our website at www.emergentbiosolutions.com under Investors/Special Events. With that introduction, I would now like to turn the call over to Fuad El-Hibri, Emergent BioSolutions’ Chairman and CEO.

Thank you, Bob. Good afternoon, everyone and thank you for joining us on our call today. For my prepared comments, I will review our financial performance for 2011, address the forecasts for 2012, including revenue expectations for the first quarter and discuss the current status of the company. To begin, let me review our financial results for 2011. For the full year, we achieved total revenues of approximately $273 million, which is within the $270 to $275 million range we provided in January. In addition, we realized net income of $23 million, which is within the $20 to $24 million range we previously provided. At year end, we held cash and accounts receivable of $220 million. Looking ahead, we are reaffirming our full year 2012 guidance of total revenues of $280 to $300 million, a split between product sales of $220 to $230 million and contracts and grants revenue of $60 to $70 million. We are also reaffirming our full year 2012 net income of $15 to $25 million. In addition, we anticipate first quarter 2012 total revenues of $40 million to $50 million. Turning now to the status of the company. Let me first talk about our BioDefense Division. In 2011, we continued to manufacture and deliver as many doses of BioThrax into the SNS as possible. To that end, we completed deliveries under the prior 17.9 million dose contract and began deliveries under the new CDC contract. The new contract, which was awarded in September, is for approximately 45 million doses valued at up to $1.25 billion to be delivered to the SNS through September 2016. This is a significant commitment by the U.S. government and further affirms BioThrax as a critical component of the government’s biopreparedness arsenal for years to come. In response to the government’s stated requirement to build a stockpile of 75 million doses of Anthrax vaccine, we continue to make progress towards licensure of our large-scale facility Building 55. This new facility is designed to manufacture up to 25 million doses of Anthrax per year on a single production line. If needed, this facility could, with the addition of a second production line, produce up to 50 million doses per year. We have presented to the FDA a comprehensive plan for regulatory approval based on comparability and non-clinical studies without clinical data. During pre-submission discussions, the FDA indicated its overall support for our plan that doesn’t require clinical studies and provided specific guidance on expanding this scope of non-clinical studies. This may translate into obtaining approval potentially one year ahead of schedule. In 2012, we’ve planned to complete consistency lot manufacturing and we anticipate licensure approval as early as 2014. The partnership with BARDA continues to enhance the value of Valtrex as one of the leading biodefense countermeasures. These initiatives include obtaining post-exposure indication, optimizing the dosing schedule, and extending the product shelf life. We are also developing Valtrex in combination with a novel adjuvant in pursuit of a two-dose vaccination schedule administered over a two-week period. In addition, with respect to our other anthrax directive programs, including our RPA vaccine candidates and our two therapeutic candidates, we plan to complete ongoing studies and secure follow-on development funding from BARDA. In pursuit of expanding the scope of our bio-defense business, we established a separate bio-defense division with its own growth objectives. We evaluate M&A opportunities targeting areas where BARDA has indicated a high degree of interest and where development contracts have been awarded. We are pursuing product development and manufacturing opportunities across multiple disease areas and are looking at products such as antimicrobials, which have the added benefit of addressing both government and commercial markets. Let me now turn to our bio-sciences division, our lead program in our bio-sciences division is MVA-85A, our TB booster vaccine candidate. Given the potential to significantly reduce the TB disease burden worldwide, our vaccine candidate has gained substantial support and funding commitments from renowned global NGOs. As you know, approximately 2 billion people or one-third of the world’s population are estimated to be infected with the bacterium and are at risk of developing TB. According to the WHO, in 2010, there were 8.8 million cases of TB resulting in 1.4 million deaths. Clearly, TB represents a substantial global unmet medical need. In 2011, with support from our partners, the Wellcome Trust and Aeras, we completed vaccination of all 2,800 infants in our phase 2b efficacy study in South Africa. These infants are now being observed and we continue to anticipate efficacy data from this study in late 2012. If these data are promising and given the heavy disease burden worldwide, we anticipate pursuing accelerated licensure in selected countries. Our TB vaccine candidate is also in a second phase 2b efficacy trial involving approximately 1,400 HIV-infected adults in South Africa and Senegal. Both clinical trials have funding support from NGOs and European government agencies. If successful, MVA-85A would be the first vaccine licensed for TB since the introduction of BCG more than eight years ago. Our other key bioscience program is our monoclonal antibiotic candidates TRU-016 targeting lymphomas. For TRU-016 in NHL and CLL, we have completed enrollment of the Phase 1b portion of the study evaluating our candidate in combination with Bendamustine in patients with relapsed CLL. The safety data from this Phase 1b portion was recently reviewed by an independent data monitoring committee, which authorized advancement into Phase II. As a result, we started dosing patients in the Phase II portion of the study, which will examine the safety and efficacy of TRU-016 with Bendamustine versus Bendamustine alone. In 2012 we expect to complete enrollment in the Phase II combination study. For TRU-016 in NHL, we have completed enrollment in a Phase 1b combination study. We expect to complete the Phase 1b study and we’ll then assess whether the data supports any initiation of Phase II in 2012. Let me now update you on our manufacturing infrastructure. We have made significant progress towards licensure of Building 55. The regulatory practices are now clear and in 2012 we plan to complete consistency lot manufacturing. We anticipate licensure could occur as early as late 2014. For our Baltimore facility, we have completed renovations and are installing disposable manufacturing technology for the simultaneous production of bacterial and viral products in multiple production-type suites. We believe disposables will improve scalability and flexibility in our production process. We have met with the FDA regarding our build-out and utilization plans, and they indicated their support for current manufacturing in the facility. Over the next 12 months, we’ve planned to introduce our first product into the facility, our MVA-85A TB vaccine candidate. In addition, the facility will be capable of manufacturing new biodefense medical countermeasures as well as our monoclonal antibiotic candidates. Before I turn this over to Don, I wanted to make brief remarks about the leadership transition that is underway at Emergent. Since 1998, it has been my great honor to serve as Emergent’s Chief Executive Officer. Therefore, it was with mixed emotions that in December last year, I announced my retirement as CEO, effective April 1, 2012. As it has always been my intention to relinquish this role; it was simply a matter of when. As our company has grown and matured, we have achieved many significant accomplishments since its inception. We have grown revenues from $2.5 million in 1998 to approaching $300 million in 2011. We have realized profitability for the last ten years. We’ve established a global footprint growing from four to over 800 employees. Our R&D pipeline has grown from zero to eight clinical-stage product candidates. And we have become the premier biodefense government contractor. I hand over the reins knowing that the company has a strong infrastructure and skilled leaders and as a result is well positioned for continued growth and success. Dan Abdun-Nabi, our current Chief Operating Officer, will assume the role of Chief Executive Officer, effective April 1, 2012. Dan and I have worked closely together for 8 years, during which time he has proven to be an accomplished leader with an extraordinary capacity to act both decisively and strategically in the company’s best interests. The Board of Directors, executives, management team and I have every confidence in his ability to continue to drive the company’s growth and to fulfill our mission to protect life. I will continue to serve as Emergent’s Executive Chairman. In this role, I will spend approximately 50% of my time leading the activities of our Board of Directors, providing ongoing advice to them and the executive team, and working with the executive team on external relations, corporate strategy, and mergers and acquisitions. That concludes my prepared comments and I will now turn it over to Don, who will take you through the numbers in greater detail.

Thank you, Fuad. Good afternoon everyone. Before I get into the financial results, I would like to congratulate Fuad on his final earnings call and thank Fuad for his support and leadership to the company since its founding. Following the close of the markets today, we released our financial results for the fourth quarter and full year 2011. I encourage everyone to take a look at the press release, which is currently available on our website. We plan to file our Annual Report on Form 10-K with the SEC no later than the close of business tomorrow, Friday, March 9th. The 10-K will also be available on our website. Let me now briefly discuss the numbers. Full year 2011 total revenues were $273.4 million versus $286.2 million in 2010. 2011 revenues were comprised of $202.4 million of product sales, a decrease of 19% over the prior year and $71 million of contracts and grants, which is an increase of 104% over the prior year. The lower product sales in 2011 is primarily due to our decision in the first quarter, as you recall, to redeploy our potency testing capacity from BioThrax release testing to qualification of replacement reference standards and other development testing, as well as to lower production output we experienced during the first half of 2011. Production output improved over the remainder of the 2011 production period, which led to increased product sales, as evidenced by our fourth-quarter product revenues of $81.6 million. Moreover, fourth-quarter 2011 total revenues were $107.9 million compared to $103.2 million in 2010. Turning to gross margins, our full year 2011 gross margin was 79%, a slight decrease over 2010. Our expectation for gross margins remains within our historic norm of between 70% and 80%. Turning to the bottom line, full year 2011 net income was $23 million, or $0.65 per share. Although this is below our 2010 net income primarily due to lower revenues, it is within the range we forecasted earlier in 2011. 2011, I’m pleased to say is our 10th consecutive year as a profitable company. Fourth-quarter 2011 net income was $28.7 million or $0.80 per share. Turning now to spending, our R&D expense for the full year 2011 was $124.8 million, a 40% increase over 2010. Fourth-quarter 2011 R&D expense was $29.4 million in line with $29.6 million spent in the fourth quarter of 2010. Recall the contracts and grants revenues and costs associated with non-controlling interests offset a portion of our R&D expenses. Taking into account these adjustments, our net R&D for full year 2011 was $47 million, which is a 6% decline from 2010. With respect to 2011 SG&A spending for the full year SG&A expenses were $74.3 million, a decrease of 3% over 2010. Fourth-quarter 2011 SG&A expenses were $18.3 million versus $21.7 million in 2010. As always, we remain focused on managing growth in our general and administrative expenses. Turning now to the balance sheet, for the full year 2011, we continued to be cash flow positive and ended the year with cash and cash equivalents plus investments of $145.9 million and an accounts receivable balance of $74.2 million. Finally, let me address our 2012 financial forecast. As Fuad noted earlier, we are reaffirming our 2012 forecast of total revenues of $280 million to $300 million and net income after tax of $15 million to $25 million. In addition, for the first quarter of 2012, we are anticipating total revenues of between $40 million and $50 million. I would like to wrap up my remarks by noting our 2011 achievements. We delivered on our government contracts. We secured a significant new procurement contract for BioThrax that provides five years of revenue visibility. We progressed in the qualification and validation of Building 55 and we advanced the development of our clinical candidates. For 2012, we look forward to building on these successes of 2011. Our business remains strong and we are confident of our prospects in 2012 in terms of financial performance, contractual success, and progress in product development. Additionally, we continue to focus on growing our business through M&A. That concludes my comments, I will now turn the call over to the operator, so that we can begin the question-and-answer portion of the call.

Hey, good afternoon guys. Thanks for taking the questions and Fuad, my congratulations to you on your retirement. First of all at BioThrax, with regard to the upcoming consistency lot manufacturing of Building 55, how long do you expect those runs are going to take and how do you think you will or how you’re expecting to disclose the result?

Thank you Cory for your kind words. To answer your question, we are in the process of gearing up consistency lot manufacturing. In addition to the consistency lots, of course, non-clinical studies need to be completed, and will be continuing to manufacture in this facility to keep it warm and to build up an inventory of product. Should we then be licensed in late 2014 to early 2015, we actually would have some product available for delivering.

Okay. And then on the model, two quick questions. One is on your first quarter revenue guidance of $40 million to $50 million, seems kind of low relative to your full-year guidance. Is this once again being driven by lower yields to start the year, is it something having to do with timing of deliveries or contract revenue or something else? And then the second one on the model, of your planned R&D spend in 2012, can you provide a rough split of how much is attributed to bio-defense related to bio-sciences? Thanks.

Yeah. Let me take your first question first, which is Q1 guidance. If you look back historically at our first quarter, it has always been less than average and the reason being is that we do our annual shutdown for maintenance every year in the September, October timeframe. So given that shutdown, the four to six weeks that we’re down usually demonstrates themselves in the first quarter. So historically, the first quarter is always a bit less than average. And with respect to the R&D spend, we don’t really break that down in terms of (audio gap). Are you still there?

Good afternoon. And congratulations, Fuad, to you as well on your new role. I sounds like you were spending a little bit more time focusing on strategy and I guess I’m just wondering what exactly that might entail, whether you’ll be looking more closely at cash redeployment, M&A, buybacks, dividends et cetera or maybe you could just describe a little bit more how you will be functioning with the company.

Thank you, Eric for the congratulations. I do look forward to transitioning to the new role and in that new role, I will be focusing mostly on the M&A piece. Of course with it has strategic, continued strategic development, we have a strategic plan that the entire executive team has worked very closely together and we are all aligned and we are executing and our strategic processes that we’re implementing and have implemented to make sure that the growth process is optimized within the organization. M&A is something that we’ve been going through; we remain acquisitive and I’ll have now more time to personally spend on evaluating candidates and once we’ve identified the right targets hopefully to negotiate and complete the deal.

Okay. Another question for Don, on the tax rate tweaked up to 41%, I think in the year 2011. Could you discuss why that might be and kind of providing a sort of directional guidance that you might want on 2012?

Sure. If you take a look back over the past few years, you’ll see that our tax rate has generally hovered around 40%. In 2010, there were a number of different adjusting activities, some from prior years that caused the rate to be below 40% for 2010. But as we take a look at our overall tax profile, unfortunately we don’t have the luxury of certain foreign operations to shelter some of this income, and a 40% rate is pretty much what we expect on average year-over-year until such time as we get into a different profile of either states or different countries that we’re doing business in.

Eric, rest assured that we are trying to manage our taxes as best as we can. We are looking at opportunities to reduce taxes, but that’s where we are.

Okay. And then last question on BioThrax. It looks like in the fourth-quarter sales were down about 9% on volumes that were down a little less than 6%. So, is that the difference between the other the delta of 3% that the difference in price between old and new contracts or partial difference price?

You’re seeing some of the ramifications, yes, Eric.

When you take a look at margins generally speaking, we expect gross margins to stay on the 70% to 80%. If you go back over the past couple of years, you will see that it has remained in that range fairly consistently. On any given quarter, you could see it spike up a couple of percentage points, and an awful lot of that is due to the four-month production cycle, where certain activities can impact gross margins that actually happened a number of months before depending upon how inventories are moving.

And to the third question regarding partnering potential for 2016, we continue to be excited about that candidate. As we’ve reported earlier, development is ongoing and we hope that the results will be promising so that we can continue development of 2016 in both disease areas. We are open to repartnering; we are looking at first generating the results and then evaluating the best timing to evaluate the whole partnering strategy.

Thank you for taking the question. I’m getting a little feedback on my line-out; it’s not on yours as well. Just on the 2016 program, can you give us a sense of when you expect to get the efficacy data there, and then what kind of hurdles are you looking for in order to take that going forward? I mean is it becoming a very competitive space where you’re looking, so I’m just wondering. I assume we’re going to see activity; the question is how much activity do you need to see to warrant moving forward?

Thank you, Jason. I have sitting here next to me Dr. Scott Stromatt, who is our Chief Medical Officer and he is very familiar with the trials associated with 2016. So I will ask him to give you greater detail.

We finished Phase 1b enrollment. You’ll see that data at APS this year. We will continue enrollment in Phase 2 and finish that this year, so we’ll have topline data next year and then obviously more data at the end of probably 2013 at one of the medical meetings. In terms of the efficacy hurdles, usually in oncology, it’s about a 30% to 50% difference in our sample size.

Thank you, Jeremy. Ladies and gentlemen that concludes today’s call. I would really appreciate everyone’s participation. Please note that today’s call is being recorded and a replay will be available beginning later today through March 22. Alternatively, there is a webcast of today’s call, an archived version of which will be available later today accessible through the company’s website again at www.emergentbiosolutions.com and clicking on Investors tab. Thank you again everyone, and we look forward to speaking to you all in the future. Goodbye.