Case study-fizek drug co

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Reference no: EM133070447

Introduction:

You are the senior financial analyst for Fizek Drug Co (Fizek). The firm develops, manufactures, and sells drugs and vaccines both in the U.S. and internationally.  You have been asked to provide answers to questions coming from the Board of Directors. These questions can be grouped into two broad categories - what projects to choose for the near future and how to finance these projects.

Deliverable:

Please present your recommendations in a report written for your supervisor, the firm Controller. Clearly show your analysis and communicate your conclusions and recommendations. Support your report by calculations in the Excel spreadsheets. In your report, explain the results of each portion of your analysis (represented by the tabs on the Excel template). Submit all the completed Excel worksheets with the completed responses to the questions posed to support your report and recommendation.

Steps to Completion:

Individual Project Analysis

Your first task is to analyze the company's three projects and provide your recommendations about their implementation.

Automation project

One of Fizek's plants is trying to decide whether to automate its drug manufacturing by purchasing a fully automated bioreactor machine complex.

The proposed machine costs $500 M and it will have a five year anticipated life and will be depreciated by using the 3-year MACRS depreciation method toward a zero salvage value. (MACRS depreciation rates are: Year 1: 33%, Year 2: 45%, Year 3: 15% and Year 4: 7%) However, the plant will be able to sell the machine in the after-market for 20% of its original costs at the end of year 5.  The firm estimates that the installation of the bioreactor will bring annual costs savings of $50 M from reduced labor costs, $10 M per year from reduced waste disposal costs, and $80 M per year from the sales byproduct of bioreactor process net of selling expenses. Fizek requires a 12% of return from its investment and has a 21% marginal tax rate.

Decision Criteria - NPV and IRR

  • Calculate the NPV and IRR for the project.
  • The manager of the plant raised some concerns about the revenues from the byproduct sale. She projects that the price of the byproduct in year 1 and the following years could be 10% to 50% less than what was projected. However, the savings from reduced labor costs and reduced waste disposal costs would remain same. She presented the following probability distribution on the projected reclaimed plastic sales: 

Remain same as projected      40%

Decrease by 10%                    30%

Decrease by 30%                    20%

Decrease by 50%                    10%

Estimate the NPV and IRR for each of these scenarios. Estimate the expected NPV. 

Break-even Analysis

  • At what volume of byproduct sales would Fizek have a break-even NPV=0?

Fiz-mRNA Vaccine

The company considers development of a new coronavirus vaccine, code-named the Fiz-mRNA which will protect from all possible mutations of coronavirus. Fizek has already spent $600 M on preliminary research for vaccine development and it will need another $600 M on development this year (tax deductible) and $2 B in CapEx  next year (these cash outlays are not part of the cash flows that you have estimated earlier, because this project is not approved yet). Capital expenditures will be depreciated over 10 years using straight line depreciation. 

The patent for the vaccine is pending and the company expects to receive an FDA approval and start selling the vaccine in two years. If approved, revenues in the first year of sales are $10 B with subsequent annual growth of 50% over the next three years (until the fourth year of sales), after which the sales will be stable between the fourth and the tenth years of sales. After that the vaccine will lose the patent protection and its manufacturing is expected to stop. The CoGS are estimated to be 15% of revenues and SG&A expenses are $2 B a year if the vaccine is produced and zero otherwise.

Expected revenues and expenses should take into account the uncertainty of getting the patent and FDA approval. The company estimates the probability of getting the approval in two years is 10% (i.e., if the company gets the approval the revenue is $10 B, if it does not, the revenue is zero, which makes the expected revenue in the first year of sales equal to $1 B). Even if Fiz-mRNA gets approved by FDA, each year there is a 5 % probability of the patent becoming obsolete due to a new vaccine entering the market, in which case the revenues, as well as CoGS and SG&A expenses will drop to zero.

NPV and IRR

  • Estimate expected revenues and costs, taking probability of approval and probability of the patent becoming obsolete into account
  • Please estimate the NPV and IRR of the Fiz-mRNA Project, using the company's WACC of 12%.

Real Option

One of your colleagues pointed out that instead of starting construction before the FDA approval, the company can invest only $0.8 B next year (depreciated over 10 years) and delay the remaining $1.2 B investment (depreciated over 8 years) for two years until the vaccine gets approved. Only if the vaccine gets approved will Fizek proceed with the second stage investment, which will take place in three years. The sales will commence in four years at the level of $10 B with subsequent annual growth of 50% over the next three years, after which the sales will be stable, but due to delay the company will lose two years of revenues. The probability of patent obsolescence remains the same as before - 5% each year.

  • What is the NPV of this two-stage investment? 

Two-stage investment alternative can be evaluated by simply calculating the NPV for two different outcomes (FDA approval or not) and then finding the expected value. Alternatively a Monte Carlo simulation can be used (see below). To check your calculations look at expected NPVs found using these two approaches - they should be nearly identical.

  • Is the option to delay the project valuable? Explain.

Monte Carlo Simulation (extra credit 5%) - ATTENTION! This part is completely optional

You want to evaluate the Fiz-mRNA Project using Monte Carlo simulation (see the template) based on probability of FDA approval in two years and patent obsolescence in each subsequent year. You can either use Crystal Ball or you are welcome to use any other software, including the Random Data generator in Data Analysis Pack.

  • What is the probability of a positive NPV? 
  • Please discuss the riskiness of the project.

NewRNA, Inc. Acquisition

The reason of the low probability of FDA approval for Fiz-mRNA is that another company, NewRNA, Inc., is working on a similar vaccine, called SuperVacc, and is very close to getting FDA approval and a patent. If NewRNA gets a patent, Fizek's own application will be denied. Therefore, instead of developing Fiz-mRNA internally, Fizek can acquire NewRNA. NewRNA already has manufacturing facilities in place and SuperVacc is its only product. The book value of the company's fixed assets is $3 B, which will be depreciated using the straight-line depreciation over the next 10 years. NewRNA expects to receive the FDA approval and patent by the end of this year with sales starting next year. Its next year revenues are expected to be $4 B ($10 B revenue in case of success times the 40% probability of success) with subsequent annual growth of 50% over the next three years (until the fourth year of sales), after which the sales will be stable until the tenth year of sales. After that the vaccine will lose the patent protection and its manufacturing is expected to stop. The CoGS are expected to be 15% of revenues and SG&A expenses are $3.5 B a year if the vaccine is produced and zero otherwise. In other words, in case of FDA approval NewRNA's revenues and costs will be similar to Fizek's, but SG&A expenses will be higher. If Fizek were to acquire NewRNA, it would be able to bring SG&A costs down to Fizek's level. The probability of FDA approval is 40% and the probability of patent obsolescence remains the same as before - 5% each year.

Mergers and Acquisitions. Target (NewRNA) Valuation

NewRNA's management would be open to the sale in the valuation range of $ 22 to 26 Billion. 

  • Please estimate NewRNA's value to Fizek, if it gets acquired.

Recommendations

Upon reviewing Fizek's choices, what project(s) would you recommend?

Venture Capital Financing 

Finally, to further reduce its risk Fizek considers keeping acquired NewRNA as a separate company. In this case Fizek will eventually shift its R&D to NewRNA, which will continue as a viable business even after the initial patent expires. Therefore, we can ignore the probability of a patent becoming obsolete. However, if FDA approval is not received this year, NewRNA will go bankrupt, in which case its fixed assets will be sold at residual book value. 

A venture capital (VC) firm Menlo Ventures is willing to provide financing of up to $5 B in acquisition of NewRNA.

If the VC agrees to invest in NewRNA, it plans to exit after eight years at which time it expects that the company's value would be eight times its year 8 EBIT.

Menlo Ventures offers three different ways of structuring the financing:

  1. Straight common stock where the VC will not receive any dividend for the first four years and will receive 20% of NOPAT as a dividend for the remaining four years. The expected tax rate for NewRNA is 21%.  In addition, the VC will receive a 20% ownership of the company's equity at the end of eight years. In the case of bankruptcy 20% ownership of the company's equity will apply to the book value immediately
  2. Redeemable convertible debt with 10% coupon rate (interest is tax-deductible). The debt will be converted for 15% ownership of the equity of NewRNA at the end of eight years. In the case of bankruptcy the debt will be immediately redeemed at its face value or at the residual assets' book value, whichever number is lower.
  3. Redeemable preferred stock with 7.5% dividend plus warrants for 15% of the equity for an exercise price of $150 M. In the case of bankruptcy the debt will be immediately redeemed at its face value or at the residual assets' book value, whichever number is lower.

Which financing method should be selected by Fizek? Should it accept Menlo Ventures offer? Explain your answer.

Frequently Asked Questions/Helpful Hints:

Is it enough to submit Excel file?

No! The deliverable outcome is your written report to the CFO. You use Excel to support your recommendations

Is there a minimum or maximum size of the report?

Although there is no formal minimum size of the report, it has to address all issues raised and provide your analysis and supporting evidence. To complete the thorough analysis required for this assignment you will probably need 3-4 pages. It is also a good idea to add a one-page executive summary to your report.

Similarly, there is no maximum limit for the report, but please avoid adding superfluous information to your report.

How do I set up Crystal Ball simulation?

Hint: use "Yes-No" distribution to create a binary (one or zero) variable indicating project continuation each year. Make revenues and costs dependent values of these binary variables.

How do I explain whether the option to delay the project valuable?

Analyze the costs and benefits of making the capital investment in two steps and delaying the project's positive cash flows by two years and shortening the revenue stream.

Are preferred dividends tax deductible?

No, unlike coupon payments, preferred dividends are not tax deductible.

How do I decide which financing option is better?

One approach would be to see which option is less costly from Fizek's management point of view.

Reference no: EM133070447

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