| (1) | Title of each class of securities to which transaction applies: | ||
|
|
|||
| (2) | Aggregate number of securities to which transaction applies: | ||
|
|
|||
| (3) | Per unit price or other underlying value of transaction computed pursuant to Exchange Act Rule 0-11 (Set forth the amount on which the filing fee is calculated and state how it was determined): | ||
|
|
|||
| (4) | Proposed maximum aggregate value of transaction: | ||
|
|
|||
| (5) | Total fee paid: | ||
|
|
| (1) | Amount Previously Paid: | ||
|
|
|||
| (2) | Form, Schedule or Registration Statement No.: | ||
|
|
|||
| (3) | Filing Party: | ||
|
|
|||
| (4) | Date Filed: |
| | A Presentation for Bellona, dated October 12, 2007 | ||
| | Strategic Alternatives Process Organizational Meeting, dated October 14, 2007 | ||
| | Biogen Idec Calendar Buyer Contact Summary (Oct./Nov. 2007) | ||
| | Biogen Idec Discussion Materials, dated October 22, 2007 | ||
| | Materials Regarding Second Round Process, dated November 2, 2007 | ||
| | Discussion Materials, dated November 4, 2007 | ||
| | Form of Letter Regarding Proposal Submission, dated November 20, 2007 | ||
| | Discussion Materials Prepared for the Board of Directors of Biogen Idec, dated December 12, 2007 |
| | October 12, 2007 | ||
| | November 8, 2007 | ||
| | November 18, 2007 | ||
| | December 9, 2007 | ||
| | December 12, 2007 |
| | Make outbound calls to prospective bidders | ||
| | Prospective bidders sign confidentiality agreements |
| | Send out information packages: |
| | Key collaboration agreements | ||
| | Tysabri data | ||
| | Other financial information? |
| | Preliminary indications of interest due, including a price range and significant contingencies |
| | Open electronic data room | ||
| | Conduct management meetings with various bidders |
| | Conduct management meetings with various bidders | ||
| | Provide draft merger agreement to bidders counsel |
| | Final bids and mark-up of agreement due | ||
| | Continue negotiations with selected bidders | ||
| | Determine whether any bidders require an opportunity to talk with Echo before signing a definitive agreement | ||
| | Discussions with Echo if and as necessary |
| 1. | Organizational Kick-off Materials | |
| 2. | Draft First Round Bid Instructions Letter | |
| 3. | Buyer Contact Summary | |
| 4. | Management Presentation Outline | |
| 5. | Preliminary Electronic Data Room Index | |
| 6. | Working Group List |
|
|
|
|
|
|
|
|
|
|
Key Parties
|
|||||
| BIIB: | Biogen Idec | |||||||
| ML: | Merrill lynch | |||||||
| GS: | Goldman Sachs | |||||||
| SS: | Shearman & Sterling | |||||||
| A: | Accountants | |||||||
| Week Of | Event | Responsible Party | ||||
|
October 15
th
|
| Organizational kick-off meeting (October 14 th ) | ||||
|
|
| Finalize potential buyer contact list (October 14 th ) | ||||
|
|
| Finalize first round bid process letter (October 14 th ) | ||||
|
|
| Finalize confidentiality agreement (October 14 th ) | ||||
|
|
| Finalize financial forecast model to be included in first round data room (October 14 th -16 th ) | REDACTED | |||
|
|
| Compile information package to be included in first round data room (October 14 th -16 th ) | ||||
|
|
| Make outbound calls to prospective bidders and receive preliminary feedback; send process letter and confidentiality agreements to prospective bidders (October 15 th ) | ||||
|
|
| Open first round data room (beginning October 17 th ) | ||||
|
|
| Continue populating data room | ||||
|
|
| Begin drafting management presentation | ||||
|
|
| Begin drafting presentation for Tysabri / Q&A calls | ||||
|
|
| Determine format for breakout sessions, including presenters from BIIB | ||||
|
October 22
nd
|
| Begin preparing second round data room | ||||
|
|
| Conduct two-hour calls on Tysabri / Q&A with interested bidders | ||||
|
|
| Begin drafting merger agreement | ||||
|
October 29
th
|
| Continue preparing second round data room and drafting merger agreement | ||||
|
November 5
th
|
| Preliminary indications of interest due November 6 th | ||||
|
|
| Board call to assess preliminary indications and discuss next steps (November 7 th ) | ||||
|
|
| Schedule management meetings | ||||
|
|
| Finalize management presentation | ||||
|
|
| Finalize second round data room | ||||
|
|
| Invite select bidders to second round of the process assuming board authorization | ||||
|
|
| Send draft merger agreement to select bidders | ||||
|
|
|
|
|
|
|
Key Parties | |||||
| BIIB: | Biogen Idec | |||||||
| ML: | Merrill Lynch | |||||||
| GS: | Goldman Sachs | |||||||
| SS: | Shearman & Sterling | |||||||
| A: | Accountants | |||||||
| Week Of | Event | Responsible Party | ||||
|
|
||||||
|
November 12
th
|
| Conduct management meetings with second round bidders | REDACTED | |||
|
|
| Make available additional information in data room to second round bidders | ||||
|
November 19
th
|
| Conduct management meetings with second round bidders | ||||
|
|
| Provide final bid instructions letter to bidders | ||||
|
|
| Respond to bidders diligence requests | ||||
|
November 26
th
|
| Respond to bidders diligence requests | ||||
|
|
| Accommodate requests for follow-up diligence calls | ||||
|
|
| [Potential conversations with Elan] | ||||
|
December 3
rd
|
| Respond to bidders diligence requests | ||||
|
|
| Accommodate requests for follow-up diligence calls | ||||
|
|
| [Potential conversations with Elan] | ||||
|
December 10
th
|
| Final bids due December 12 th | ||||
|
|
| Continue negotiations with selected bidders | ||||
|
|
| [Potential conversations with Elan] | ||||
|
|
| Board meeting to review final bids and decide on next steps | ||||
|
December 17
th
|
| Board meeting to approve the transaction | ||||
|
|
| Financial advisors render fairness opinions | ||||
|
|
| Execute a definitive merger agreement | ||||
|
|
| Announce transaction | ||||
|
|
|
| | As you know, Biogen Idecs Board of Directors has authorized management to assess strategic alternatives, including a potential sale of the Company | |
| | Biogen Idec has retained Merrill Lynch and Goldman Sachs as its financial advisors to help with the process | |
| | The Company has already received several inquiries from select parties with regards to a potential business, combination | |
| | Moreover, given Biogen Idecs attractiveness as a unique asset, we believe there will be strong interest from other parties, resulting in a highly competitive process |
| | Leadership in immunology, neurology and oncology, and a promising pipeline in additional attractive areas such as inflammation, cardiovascular and hematology | ||
| | Has meaningful economics from 2 blockbusters, Avonex and Rituxan, with Tysabri representing a potential blockbuster as well | ||
| | Has global biologics commercial and development infrastructure | ||
| | Has strong research & development capability, depth and breadth with over 20 products in clinical development | ||
| | Has strong revenue, profit and cash flow growth, all exceeding major pharma growth |
|
|
|
| | We believe Biogen Idecs partner Elan will also cooperate in this process |
| | We believe Elan is unlikely to exercise its change of control rights relating to Tysabri if an offer for the Company is made in the near future | ||
| | We believe Elan is willing to negotiate a new type of agreement for Tysabri with a new partner |
| | While Genentech has the right to buy back Biogen Idecs share of Rituxan in a change of control situation, we believe Genentech is unlikely to exercise its option based on financial incentives of the collaboration agreement | |
| | Merrill Lynch and Goldman Sachs will be facilitating an expedited process, given the current momentum and strong interest from certain parties, with a goal of receiving first round, non-binding bids on November 6 th and completing the process by mid-December |
| | Given your position as a leading company in the pharma space, we would like to assess your interest in pursuing a strategic transaction with the Company | ||
| | If your organization is interested, Merrill Lynch and Goldman Sachs can facilitate next steps | ||
| | We have a draft confidentiality agreement (CDA) and process letter that we will send you | ||
| | Once the CDA has been executed, you will be given access via a data room to non-public first round information including Biogen Idecs long-range plan, review of pipeline, [Tysabri-related information], biologics capabilities and unredacted versions of collaboration agreements |
|
|
|
| | Responses to potential questions regarding Carl Icahns communications with / bid for Biogen Idec |
| | The Company has received expressions of interest from several strategic and financial buyers, including an offer from Carl Icahn | ||
| | Hence the Board of Directors has initiated a process to evaluate third party interest in the Company in order to maximize shareholder value | ||
| | Icahn made a non-binding offer for Biogen Idec [at a price range that provided a standard premium to the current price and he requested further diligence] | ||
| | Icahn also mentioned his understanding that Elan would cooperate in a sale process, i.e., would not exercise its change of control rights relating to Tysabri |
| | Responses to potential questions regarding interest from / bids from strategic buyers |
| | Biogen Idec has received several overtures from large strategic players regarding a potential acquisition of the Company |
|
|
|
5
|
|
|
| 1. | Purchase Price and Valuation: Your Indication of Interest should specify the price per share in U.S. dollars which you would pay at closing to acquire 100% of the fully diluted common stock of the Company. Please specify all material assumptions and material contingencies you have taken into account in arriving at your preliminary indication of value; |
| 2. | Consideration: The structure of your proposal, including cash and/or stock consideration. While the Companys principal objective is to maximize shareholder value, on the margin cash consideration will be preferred; |
| 3. | Sources and Structure of Financing: The expected sources of funds (with as much specificity as possible), the timing involved and the steps necessary to secure the funds. Please note that the Company fully expects to enter into a binding purchase agreement that is not subject to any financing and due diligence contingencies; |
| 4. | Due Diligence : A detailed description of the additional due diligence you would require in order to submit a definitive proposal, including a specific list of additional information and due diligence requirements; |
| 5. | Required Approvals: Any anticipated corporate, shareholder or regulatory approvals you would need prior to executing definitive transaction documentation, as well as any additional approvals or other conditions you would need to close a transaction; |
| 6. | Material Conditions : Any material conditions to consummation of your proposed acquisition of the Company; |
| 7. | Contact Information: A list of key individuals within your organization and your team of advisors with whom we may discuss your Indication of Interest; |
| 8. | Submission Deadline : Your Indication of Interest should be submitted on or before 12:00 p.m. Eastern Daylight Time, Tuesday, November 6, 2007 to the attention of: |
|
Alan Hartman
Managing Director Head of US M&A alan_hartman@ml.com Tel: (212) 449-8585 Fax: (212) 449-9283 |
Robert King
Managing Director Co-Head of Global Healthcare robert.king@gs.com Tel: (212) 902-3377 Fax: (212) 902-3000 |
| 9. | Additional Information: Any other information which you believe might be relevant to Biogen Idec, Merrill Lynch and Goldman Sachs in evaluating your Indication of Interest. |
|
Alan Hartman
|
Robert King |
|
Merrill Lynch
&
Co.
4 World Financial Center, North Tower 250 Vesey Street New York, NY 10080 |
Goldman Sachs
&
Co.
85 Broad Street New York, NY 10004 |
|
|
Alan Hartman
Managing Director Head of US M&A alan_hartman@ml.com Tel: (212) 449-8585 Fax: (212) 449-9283 |
Robert King
Managing Director Co-Head of Global Healthcare robert.king@gs.com Tel: (212) 902-3377 Fax: (212) 902-3000 |
|
|
Mark Robinson
Managing Director Head of Global Healthcare mark_j_robinson@ml.com Tel: (415) 676-3379 Fax: (415) |
Marshall Smith
Managing Director marshall.smith@gs.com Tel: (212) 902-1250 Fax: (212) 902-3000 |
|
|
Ivan Farman
Managing Director ivan_farman@ml.com Tel: (212) 449-8897 Fax: (212) 449-3307 |
Tosa Ogbomo
Managing Director tosa.ogmobo@gs.com Tel: (212) 902-2079 Fax: (212) 902-3000 |
| Stage | ||||||||||||||||||||||
| Final Bid | ||||||||||||||||||||||
| Prelim. | Initial | Process | ||||||||||||||||||||
| Bid | Data | Two-Hour | 2nd Round | Letter / | ||||||||||||||||||
| Process | Room | Tysabri / | Initial | Data Room | Management | Merger | Final | |||||||||||||||
| Confi | Letter | Confl | Access | Q&A | Indication | Access | Presentation | Agreement | Bid | |||||||||||||
| Company | Contacted | Sent | Sent | Received | Granted | Session | Recd | Granted | Conducted | Sent | Received | |||||||||||
| Buyer | Buyer Contact(s) | GS Rep | Date Contacted | Status | ||||
| Buyer | Buyer Contact(s) | ML Rep | Date Contacted | Status | ||||
| | Introductions |
| | Agenda showing sections, with names and titles of presenters |
| | Company Overview |
| | Key company investment highlights; 5-6 high level bullet points on Bellona | ||
| | 3-5 pages overview slides | ||
| | Summary of 2007-2010 strategy goals |
| | Neurology/Immunology franchise | |
| | Oncology franchise | |
| | R&D |
| | Overall R&D Strategy | ||
| | Pipeline overview | ||
| | Pipeline detail and review of key product candidates by TA: stage, indication, clinical data, any projected milestones | ||
| | R&D resources (manpower, allocation between functions) | ||
| | Business development activities |
| | Manufacturing, Facilities and Operations |
| | Manufacturing capabilities, capacity, flexibility | ||
| | Overview of supply chain | ||
| | Real estate overview |
| | Capex forecast 2007-2009 | ||
| | HR headcount by function |
| | Financial review |
| | Overview of systems and controls | ||
| | Historical Financials |
| | 3-year historical financials | ||
| | Discussion of historical trends by line item (COGS, R&D, S&M, G&A) |
| | Financial Projections |
| | Financial growth drivers | ||
| | 2007-20XX financial projections with revenue by product | ||
| | Key assumptions underlying 2007-20XX forecasts | ||
| | R&D and SG&A leverage assumptions |
| | Conclusions |
| Biogen | |||||||||||||||
| Description | Idec | S&S | Public | ||||||||||||
|
1. General Corporate
|
|||||||||||||||
|
1.1. Organizational Charts
|
|||||||||||||||
|
1.1.1. Biogen Idec Inc. Corporate Structure Chart,
dated as of July 1, 2007 Domestic, Foreign Operations
|
|||||||||||||||
|
1.2. Certificate of Incorporation and By-laws
|
|||||||||||||||
|
1.3. Corporate Governance
|
|||||||||||||||
|
1.3.1. Meeting Minutes
|
REDACTED | ||||||||||||||
|
1.3.1.1. Minutes of Annual Meeting of Stockholders of Biogen
Idec Inc.,
dated June 16, 2004
|
|||||||||||||||
|
1.3.1.2. Minutes of Annual Meeting of Stockholders of Biogen Idec
Inc.,
dated May 25, 2006
|
|||||||||||||||
|
1.3.2. Charters
|
|||||||||||||||
|
1.3.2.1. Biogen Idec Inc. Corporate Governance Principles
|
|||||||||||||||
|
1.3.2.2. Biogen Idec Inc. Code of Business Conduct
|
|||||||||||||||
|
1.3.3. Reports
|
|||||||||||||||
| Biogen | |||||||||||||||
| Description | Idec | S&S | Public | ||||||||||||
|
1.4.2. Minutes and Charters
|
|||||||||||||||
|
1.4.2.1.
|
|||||||||||||||
|
1.4.2.2
|
|||||||||||||||
|
1.4.3. Material Agreements
|
|||||||||||||||
|
1.4.4. Sales & Distributions
|
|||||||||||||||
|
1.5. Capital Structure
|
|||||||||||||||
|
1.5.1. 2007 Share Calculation Report, dated September
30,2007, Reflecting Both Basic and Diluted Shares
Outstanding
|
|||||||||||||||
|
2. Products and Collaboration Agreements
|
REDACTED | ||||||||||||||
|
2.1. Avonex
|
|||||||||||||||
|
2.1.1. Material Agreements
|
|||||||||||||||
|
2.1.2. Program Documentation
|
|||||||||||||||
|
2.1.3. Sales & Distributions
|
|||||||||||||||
|
2.1.4. Research and Development (including Safety Data)
|
|||||||||||||||
|
2.1.4.1.
|
|||||||||||||||
|
2.1.5. Marketing
|
|||||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
2.2. Rituxan (Genentech)
|
||||||||||||
|
2.2.1. Material Agreements
|
||||||||||||
|
2.2.1.1
|
||||||||||||
|
2.2.1.2.
|
||||||||||||
|
2.2.1.3.
|
||||||||||||
|
2.2.2. Program Documentation
|
||||||||||||
|
2.2.3. Sales & Distributions
|
REDACTED | |||||||||||
|
2.2.4. Research and Development (including Safety Data)
|
||||||||||||
|
2.2.5. Marketing
|
||||||||||||
|
2.3. Tysabri (Elan)
|
||||||||||||
|
2.3.1. Material Agreements
|
||||||||||||
|
2.3.1.1.
|
||||||||||||
|
2.3.1.2
|
||||||||||||
|
2.3.2. Program Documentation
|
||||||||||||
|
2.3.3. Sales & Distributions
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
2.3 4. Research and Development (including Safety Data)
|
||||||||||||
|
2.3.4.1.
|
||||||||||||
|
2.3.5. Marketing
|
||||||||||||
|
2.4. Fumaderm
|
||||||||||||
|
2.4.1. Material Agreements
|
||||||||||||
|
2.4.2. Program Documentation
|
||||||||||||
|
2.4.3. Sales & Distributions
|
REDACTED | |||||||||||
|
2.4.4. Research and Development (including Safety Data)
|
||||||||||||
|
2.4.5. Marketing
|
||||||||||||
|
2.5. BG-12
|
||||||||||||
|
2.5.1. Material Agreements
|
||||||||||||
|
2.5.2. Program Documentation
|
||||||||||||
|
2.5.3. Sales & Distributions
|
||||||||||||
|
2.5.4. Research and Development (including Safety Data)
|
||||||||||||
|
2.5.5. Marketing
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
2.6. Anti-CD80 MAb/galizimab
|
||||||||||||
|
2.6.1. Material Agreements
|
||||||||||||
|
2.6.2. Program Documentation
|
||||||||||||
|
2.6.3. Sales & Distributions
|
||||||||||||
|
2.6.4. Research and Development (including Safety Data)
|
||||||||||||
|
2.6.5. Marketing
|
||||||||||||
|
2.7. Anti-CD23 MAb/lumiliximab
|
||||||||||||
|
2.7.1. Material Agreements
|
REDACTED | |||||||||||
|
2.7.2. Program Documentation
|
||||||||||||
|
2.7.3. Sales & Distributions
|
||||||||||||
|
2.7.4. Research and Development (including Safety Data)
|
||||||||||||
|
2.7.5. Marketing
|
||||||||||||
|
2.8. PDL Biopharma Phase II Products (Volociximab, Daclizumab)
|
||||||||||||
|
2.8.1. Material Agreements
|
||||||||||||
|
2.8.2. Program Documentation
|
||||||||||||
| Biogen | ||||||
| Description | Idec | S&S | Public | |||
|
2.8.3. Sales & Distributions
|
||||||
|
2.8.4. Research and Development (including Safety Data)
|
||||||
|
2.8.5. Marketing
|
||||||
|
2.9. Other Commercial Pipeline Products
|
||||||
|
2.9.1. Material Agreements
|
||||||
|
2.9.1.1.
|
||||||
|
2.9.1.2.
|
REDACTED | |||||
|
2.9.1.3.
|
||||||
|
2.9.1.4.
|
||||||
|
2.9.1.5.
|
||||||
|
2.9.1.6.
|
||||||
|
2.9.1.7.
|
||||||
|
2.9.1.8.
|
||||||
|
2.9.1.9.
|
||||||
|
2.9.1.10.
|
7
| Biogen | ||||||
| Description | Idec | S&S | Public | |||
|
2.9.1.11.
|
||||||
|
2.9.1.12.
|
||||||
|
2.9.1.13.
|
||||||
|
2.9.1.14.
|
||||||
|
2.9.1.15.
|
||||||
|
2.9.1.16.
|
||||||
|
2.9.1.17.
|
REDACTED | |||||
|
2.9.1.18.
|
||||||
|
2.9.1.19.
|
||||||
|
2.9.1.20.
|
||||||
|
2.9.1.21.
|
||||||
|
2.9.1.22.
|
||||||
|
2.9.1.23.
|
||||||
|
2.9.1.24.
|
||||||
|
2.9.1.25.
|
8
| Biogen | ||||||
| Description | Idec | S&S | Public | |||
|
2.9.1.26.
|
||||||
|
2.9.1.27.
|
||||||
|
2.9.1.28.
|
||||||
|
2.9.1.29.
|
||||||
|
2.9.1.30.
|
||||||
|
2.9.1.31.
|
||||||
|
2.9.1.32.
|
REDACTED | |||||
|
2.9.1.33.
|
||||||
|
2.9.1.34.
|
||||||
|
2,9.1.35.
|
||||||
|
2.9.1.36.
|
||||||
|
2.9.1.37.
|
||||||
|
2.9.1.38.
|
||||||
|
2.9.1.39.
|
||||||
|
2.9.1.40.
|
9
| Biogen | ||||||
| Description | Idec | S&S | Public | |||
|
2.9.1.41.
|
||||||
|
2.9.1.42.
|
||||||
|
2.9.1.43.
|
||||||
|
2.9.1.44.
|
||||||
|
2.9.1.45.
|
||||||
|
2.9.1.46.
|
||||||
|
2.9.1.47.
|
||||||
|
2.9.1.48.
|
REDACTED | |||||
|
2.9.1.49.
|
||||||
|
2.9.1.50.
|
||||||
|
2.9.1.51.
|
||||||
|
2.9.1.52.
|
||||||
|
2.9.1.53.
|
||||||
|
2.9.1.54.
|
||||||
|
2.9.1.55.
|
10
11
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
3.5. Tax Returns 2006
|
||||||||||||
|
3.5.1. 2006 Form 8453-C U.S. Corporation Income Tax Declaration for an IRS
e-file
Return
for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.2. 2006 Form 1120 U.S. Corporate Income Tax Return for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.3. 2006 Form 4626 Alternative Minimum Tax-Corporations for Biogen Idec Inc. &
Subsidiaries
|
||||||||||||
|
3.5.4. 2006 Form 851 Affiliations Schedule for Biogen Idec Inc.
|
||||||||||||
|
3.5.5. 2006 Forms 1118 Foreign Tax Credit-Corporations for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.6. 2006 Form 1122 Authorization and Consent of Subsidiary Corporation To Be Included
in a Consolidated Income Tax Return for Conforma Therapeutics Corporation
|
REDACTED | |||||||||||
|
3.5.7. 2006 Form 2220 Underpayment of Estimated Tax by Corporations for Biogen Idec Inc.
& Subsidiaries
|
||||||||||||
|
3.5.8. 2006 Form 3800 General Business Credit for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.9. 2006 Form 4562 Depreciation and Amortization (Including Information on Listed
Property) for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.10. 2006 Form 4797 Sale of Business Property for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.11. 2006 Forms 6765 Credit for Increasing Research Activities for Biogen Idec Inc. &
Subsidiaries
|
||||||||||||
|
3.5.12. 2006 Form 8275-R Regulation Disclosure Statement for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.13. 2006 Form 8820 Orphan Drug Credit for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.14. 2006 Form 8858 Information Return of U.S. Persons With Respect To Foreign
Disregarded Entities for Biogen Idec MA Inc.
|
||||||||||||
12
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
3.5.15. 2006 Form 8883 Asset Allocation Statement Under Section 338 for Biogen Idec MA Inc.
|
||||||||||||
|
3.5.16. 2006 Form 8903 Domestic Production Activities Deduction for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.17. 2006 Form 8913 Credit for Federal Telephone Excise Tax Paid for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.5.18. 2006 Forms 8916-A Reconciliation of Cost Goods Sold Reported on Schedule M-3 for Biogen Idec Inc.
|
||||||||||||
|
3.5.19. 2006 Forms 926 Return by a U.S. Transferor of Property to a Foreign Corporation for Biogen Idec
MA Inc.
|
||||||||||||
|
3.5.20. Attachments to 2006 Tax Returns
|
||||||||||||
|
3.5.21. 2006 Form 8865 Return of U.S. Persons With Respect to Certain Foreign Partnerships for Biogen
Idec MA Inc.
|
REDACTED | |||||||||||
|
3.6. Tax Returns 2005
|
||||||||||||
|
3.6.1. 2005 Form 1120 U.S. Corporate Income Tax Return for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.6.2. 2005 Form 8453-C U.S. Corporation Income Tax Declaration for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.6.3. 2005 Form 851 Affiliations Schedule for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.6.4. 2005 Forms 1118 Foreign Tax Credit-Corporations for Biogen Idec Inc.
|
||||||||||||
|
3.6.5. 2005 Form 2220 Underpayment of Estimated Tax by Corporations for Biogen Idec Inc.
|
||||||||||||
|
3.6.6. 2005 Form 3800 General Business Credit for Biogen Idec Inc.
|
||||||||||||
|
3.6.7. 2005 Form 4562 Depreciation and Amortization (Including Information on Listed Property) for
Biogen Idec Inc.
|
||||||||||||
13
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
3.6.8. 2005 Form 4626 Alternative Minimum Tax-Corporations for Biogen Idec Inc.
|
||||||||||||
|
3.6.9. 2005 Form 4797 Sale of Business Property for Biogen Idec Inc.
|
||||||||||||
|
3.6.10. 2005 Form 6765 Credit for Increasing Research Activities for Biogen Idec Inc.
|
||||||||||||
|
3.6.11. 2005 Form 8275-R Regulation Disclosure Statement for Biogen Idec Inc.
|
||||||||||||
|
3.6.12. 2005 Form 8820 Orphan Drug Credit for Biogen Idec Inc.
|
||||||||||||
|
3.6.13. 2005 Form 8827 Credit for Prior Year Minimum Tax-Corporations for Biogen Idec Inc.
|
||||||||||||
|
3.6.14. 2005 Form 8858 Information Return of U.S. Persons With Respect To Foreign
Disregarded Entities for Biogen Idec Inc. & Subsidiaries
|
||||||||||||
|
3.6.15. 2005 Form 8895 One-Time Dividends Received Deduction for Certain Cash Dividends
from Controlled Foreign Corporations for Biogen Idec Inc.
|
REDACTED | |||||||||||
|
3.6.16. 2005 Form 8903 Domestic Production Activities Deduction for Biogen Idec Inc.
|
||||||||||||
|
3.6.17. 2005 Form 926 Return by a U.S. Transferor of Property to a Foreign Corporation for
Biogen Idec MA Inc.
|
||||||||||||
|
3.6.18. 2005 Forms 8621 Return by a Shareholder of a Passive Foreign Investment Company or
Qualified Electing Fund for Biogen Idec MA Inc
|
||||||||||||
|
3.6.19. Attachments to 2005 Tax Returns
|
||||||||||||
|
3.7. Audit Related
|
||||||||||||
|
3.7.1.
|
||||||||||||
|
3.7.2.
|
||||||||||||
14
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
3.7.3.
|
||||||||||||
|
3.7.4.
|
||||||||||||
|
3.7.5.
|
||||||||||||
|
3.7.6.
|
||||||||||||
|
3.7.7.
|
||||||||||||
|
3.7.8.
|
||||||||||||
|
3.7.9.
|
||||||||||||
|
4. Research and Development
|
REDACTED | |||||||||||
|
4.1. R&D Day 2007 Presentation
|
||||||||||||
|
4.2. Pipeline Products (Ongoing Studies, Preclinical and Clinical Data, Trials)
|
||||||||||||
|
4.2.1. Oncology
|
||||||||||||
|
4.2.2. Immunology and Autoimmune and Inflammatory Diseases
|
||||||||||||
|
4.2.3. Neurology and Neurobiology
|
||||||||||||
|
4.2.4. Emerging Therapeutic Areas
|
||||||||||||
|
4.3. Budgets
|
||||||||||||
15
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
4.3.1. Oncology
|
||||||||||||
|
4.3.2. Immunology and Autoimmune and Inflammatory Diseases
|
||||||||||||
|
4.3.3. Neurology and Neurobiology
|
||||||||||||
|
4.3.4. Emerging Therapeutic Areas
|
||||||||||||
|
5. Intellectual Property
|
||||||||||||
|
5.1. Summary of Key IP (Owned/Licensed)
|
||||||||||||
|
5.1.1. List of Trademarks
|
REDACTED | |||||||||||
|
5.1.2. Docket list of Patents
|
||||||||||||
|
5.2. Patents Applications, Approvals, Renewals
|
||||||||||||
|
5.2.1.
|
||||||||||||
|
5.3. License Agreements
|
||||||||||||
|
5.3.1. J
|
||||||||||||
|
5.3.2.
|
||||||||||||
|
5.3.3.
|
||||||||||||
|
5.3.4.
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
5.4.
|
||||||||||||
|
6. Legal Regulatory and Compliance
|
||||||||||||
|
6.1. Litigation (excluding IP)
|
||||||||||||
|
6.1.1.
|
||||||||||||
|
6.1.2.
|
||||||||||||
|
6.1.3.
|
||||||||||||
|
6.1.4.
|
||||||||||||
|
6.1.5.
|
REDACTED | |||||||||||
|
6.1.6.
|
||||||||||||
|
6.1.7.
|
||||||||||||
|
6.1.8.
|
||||||||||||
|
6.1.9.
|
||||||||||||
|
6.1.10
|
||||||||||||
|
6.2. Regulatory and Compliance
|
||||||||||||
|
6.2.1. Food and Drug Administration
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
6.2.1.1. List of approved countries for commercial products
|
||||||||||||
|
6.2.1.2. List of all U.S. wholesale and manufacturer licenses
|
||||||||||||
|
6.2.1.3. Active state manufacturer, wholesaler distributor
licenses held by BIIB or BIUS
|
||||||||||||
|
6.2.1.4. US FDA Drug Establishment Registrations and US
FDA License Number
|
||||||||||||
|
6.2.1.5. US FDA and EU EMEA inspections that took place at the
BIIB Cambridge and RTP sites within the period of January 1, 2003
to June 12, 2007
|
||||||||||||
|
6.2.2. National Institutes of Health Guidelines for Research
Involving Recombitant DNA
|
||||||||||||
|
6.2.3. Securities and Exchange Commission
|
||||||||||||
|
6.2.3.1.
|
||||||||||||
|
6.2.3.2
|
||||||||||||
|
6.2.3.3.
|
||||||||||||
|
6.2.3.4
|
REDACTED | |||||||||||
|
6.2.3.5.
|
||||||||||||
|
6.2.3.6.
|
||||||||||||
|
6.2.3.7.
|
||||||||||||
|
6.2.3.8.
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
6.2.3.9.
|
||||||||||||
|
6.2.3.10.
|
||||||||||||
|
6.2.3.11.
|
||||||||||||
|
6.2.3.12.
|
||||||||||||
|
6.2.4.
|
||||||||||||
|
6.2.5. Medicaid Rebate Program
|
||||||||||||
|
6.2.6. Environmental Health and Safety Information
|
||||||||||||
|
6.2.6.1. Cambridge Public Health Department Recombinant DNA Users Permit
|
||||||||||||
|
6.2.6.2. Massachusetts Department of Environmental Protection
Air Emissions
Permits
|
REDACTED | |||||||||||
|
6.2.6.3. Massachusetts Department of Public Health Radioactive
Materials
License
|
||||||||||||
|
6.2.6.4. Cambridge License Commission Flammable Materials Storage License
|
||||||||||||
|
6.2.6.5. US Department of Justice Drug Enforcement
Controlled Substance
License
|
||||||||||||
|
6.2.6.6. Massachusetts Department of
Public Health, Division of Food and
Drugs Controlled
Substance License
|
||||||||||||
|
6.2.6.7. Massachusetts Water Resources
Authority Wastewater Discharge
Permits
|
||||||||||||
|
6.2.6.8. Cambridge Public Health Department Recombinant DNA Users Permit
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
6.2.6.9.
|
||||||||||||
|
6.2.6.10
|
||||||||||||
|
6.2.6.11.
|
||||||||||||
|
6.2.6.12.
|
||||||||||||
|
6.2.6.13. BIIB Hillerod Licenses Inspection Documents and Certificates
|
||||||||||||
|
6.2.6.14
|
||||||||||||
|
6.2.6.15. RTP North Carolina Air Permit No.
|
REDACTED | |||||||||||
|
6.2.6.16. RTP North Carolina Radioactive Materials License
|
||||||||||||
|
6.2.6.17. Cary, North Carolina Industrial
Discharge Pretreatment Permit Extension
|
||||||||||||
|
6.2.6.18.
|
||||||||||||
|
6.2.6.19.
|
||||||||||||
|
6.2.6.20. RTP North Carolina Air Permit No.
|
||||||||||||
|
6.2.6.21.
|
||||||||||||
|
6.2.6.22.
|
||||||||||||
|
6.2.6.23.
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
6.2.6.24.
|
||||||||||||
|
6.2.6.25.
|
||||||||||||
|
6.2.6.26.
|
||||||||||||
|
6.2.6.27.
|
||||||||||||
|
6.2.6.28.
|
||||||||||||
|
6.2.6.29.
|
||||||||||||
|
6.2.6.30.
|
REDACTED | |||||||||||
|
6.2.6.31.
|
||||||||||||
|
6.2.6.32.
|
||||||||||||
|
6.2.6.33.
|
||||||||||||
|
6.2.6.34.
|
||||||||||||
|
6.2.6.35.
|
||||||||||||
|
6.2.6.36.
|
||||||||||||
|
6.2.6.37.
|
||||||||||||
|
6.2.6.38.
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
6.2.6.39.
|
||||||||||||
|
6.2.6.40.
|
||||||||||||
|
6.2.6.41.
|
||||||||||||
|
6.2.6.42.
|
||||||||||||
|
6.2.6.43.
|
REDACTED | |||||||||||
|
6.2.6.44.
|
||||||||||||
|
6.2.6.45.
|
||||||||||||
|
6.2.6.46.
|
||||||||||||
|
6.2.6.47.
|
||||||||||||
|
6.2.6.48.
|
||||||||||||
|
6.2.7. Other Regulatory
|
||||||||||||
|
6.2.7.1.
|
||||||||||||
|
6.2.7.2.
|
||||||||||||
|
6.2.7.3.
|
||||||||||||
|
6.2.7.4.
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
7.3. Employment Agreements
|
||||||||||||
|
7.3.1. Executive Agreements
|
||||||||||||
|
7.3.1.1.
|
||||||||||||
|
7.3.1.2.
|
||||||||||||
|
7.3.1.3.
|
||||||||||||
|
7.3.1.4.
|
||||||||||||
|
7.3.1.5.
|
REDACTED | |||||||||||
|
7.3.1.6.
|
||||||||||||
|
7.3.1.7.
|
||||||||||||
|
7.3.1.8.
|
||||||||||||
|
7.3.1.9.
|
||||||||||||
|
7.3.1.10.
|
||||||||||||
|
7.3.1.11.
|
||||||||||||
|
7.3.1.12.
|
||||||||||||
|
7.3.2. Non-Executive Agreements (including Form Agreements)
|
||||||||||||
| Biogen | ||||||||||||
| Description | Idec | S&S | Public | |||||||||
|
7.4. Plans
|
||||||||||||
|
7.4.1. Summary Description of Biogen Idec Inc. 2005 Omnibus Equity Plan
|
||||||||||||
|
7.4.2. Biogen Idec Inc. 2005 Omnibus Equity Plan with Amendment
|
||||||||||||
|
7.4.3. Biogen Idec Inc. (Formerly Idec Pharmaceuticals
Corporation) Amended and
Restated 1995 Employee Stock Purchase Plan, dated as of April 6,2005
|
||||||||||||
|
7.4.4. Biogen Idec Inc. Revised Plan Summary and Prospectus of Amended and
Restated 1995 Employee Stock Purchase Plan, dated June 18, 2007
|
||||||||||||
|
7.4.5. IDEC Pharmaceuticals Corporation 1993 Non-Employee
Directors Stock Option Plan (amended and restated through February 19, 2003)
|
REDACTED | |||||||||||
|
7.5. Schedules
|
||||||||||||
|
7.5.1. Biogen Idec Inc. Stock Option Summary
Spreadsheet of Outstanding Shares
|
||||||||||||
|
7.6. Benefit Plans (Health and Welfare, 401(k) and ERISA)
|
||||||||||||
|
8. Real Property and Manufacturing
|
||||||||||||
|
8.1. Summaries of Owned and Leased Real Property
|
||||||||||||
|
8.1.1. Biogen Idec Inc. Real Estate Portfolio Report
|
||||||||||||
|
8.1.2. Biogen Idec Inc. List of Leases and Subleases
|
||||||||||||
|
8.2. Owned Real Property
|
||||||||||||
|
8.3. Leases
|
||||||||||||
| Biogen | ||||||
| Description | Idec | S&S | Public | |||
|
9.1 Summaries
|
||||||
|
9.1.1.
|
||||||
|
9.1.2.
|
||||||
|
9.2. 2003 Merger
|
||||||
|
9.2.1.
|
||||||
|
9.3. Conforma Acquisition
|
REDACTED | |||||
|
9.4. Fumapharm Acquisition
|
||||||
|
9.5. Syntonix
|
||||||
|
9.5.1.
|
||||||
|
10. Insurance & Risk Management
|
||||||
|
10.1.1. Summaries
|
||||||
|
10.1.1.1.
|
||||||
|
10.1.1.2.
|
||||||
|
10.1.1.3.
|
||||||
|
10.1.2. Insurance Polices
|
27
| Biogen | ||||||
| Description | Idec | S&S | Public | |||
|
10.1.3. Self-Insurance Programs
|
28
|
|
|
Buyer Contact Summary (Oct / Nov 2007)
Sunday
Monday
Tuesday
Wednesday
Thursday
Friday
Saturday
22 October
23
24
25
26
REDACTED
Earnings Release
[TBD]: Buyer 1 Call
[TBD]: Buyer 3 Call
[TBD]
[TBD]: Buyer 2 Call
[TBD]: Buyer 4 Call
[TBD]: Buyer 6 Call
29
30
31
1
November
2
[TBD]: Buyer 7 Call
[TBD]: Buyer 9 Call
[TBD]: Buyer 11 Call
[TBD]: Buyer 8 Call
[TBD]: Buyer 10 Call
[TBD]: Buyer 12 Call
5
6
7
8
9
1
st
Round Bids Due
l2
13
14
15
16
Management
Management
Management
Management
Management
Presentation
Presentation
Presentation
Presentation
Presentation
19
20
21
22
23
Management
Management
[Management
Thanksgiving
Presentation
Presentation
Presentation]
Buyer 2 Hour Call Schedule
Buyer
Buyer Participants
1) Buyer
[Time & Dial-in TBD]
[TBD]
2) Buyer
[Time & Dial-in TBD]
[TBD]
3) Buyer
[Time & Dial-in TBD]
[TBD]
4) Buyer
[Time & Dial-in TBD]
[TBD]
5)
[Time & Dial-in TBD]
REDACTED
6) Buyer
[Time & Dial-in TBD]
[TBD]
7) Buyer
[Time & Dial-in TBD]
[TBD]
8) Buyer
[Time & Dial-in TBD]
[TBD]
Buyer 2 Hour Call Schedule (Contd)
Date
Buyer
Time / Dial-In
Buyer Participants
9) Buyer
[Time & Dial-in TBD]
[TBD]
10) Buyer
[Time & Dial-in TBD]
[TBD]
11) Buyer
[Time & Dial-in TBD]
[TBD]
12) Buyer
[Time & Dial-in TBD]
[TBD]
| I. | Calendar and Work Stream Update | |
| II. | Buyer Update | |
| III. | Round I Two-hour Conference Calls |
| | |||
| | |||
| |
| IV. | Round II review |
| | |||
| | |||
| |
| | REDACTED |
| | |||
| | |||
| | |||
| |
| V. |
| | |||
| |
| | October 12, 2007: Public announcement of process | |
| | All identified buyers contacted and initial feedback on interest received | |
| | CA process nearing completion | |
| | Several conversations with Elan / Lehman Brothers | |
| | First round data room open and access granted as CAs are signed | |
| | First round management presentation circulated | |
| | First round 2 hour calls starting October 24 th (currently being scheduled) | |
| | First round bids on November 6 |
Primary
Date Yet To be
Event
Responsibility
Scheduled?
1
st
Round 2 Hour Calls
2
nd
Round Data Room
Management Presentations
Finalize management presentation
Schedule presentation rehearsal
Logistics (hotels, conference rooms etc).
Initial Draft of Merger Agreements
REDACTED
Board Communication
Update on process
Review of 1st round bids
Review final bids
Approve transaction
Communication with Elan / Genentech
Reverse Due Diligence (if needed)
REDACTED
Stage
Parties
Contacted Parties
Sent CAs to Parties
CAs Under Active Negotiations
REDACTED
CAs signed
Data Room access granted
| | Round II presentations scheduled for week of November 12th and 19th |
| | To schedule presentation rehearsals |
| | Break-out sessions post management presentation (schedule in following page) | |
| | Location of management presentations in Boston |
| | Currently working on hotel logistics |
| | Buyer diligence requests will come initially to the bankers |
| | Diligence request log created for all requests (template in following pages) |
Name
Position
Mgt Presentation
Break-out
President, CEO
ü
President, R&D
ü
REDACTED
EVP, Finance & CFO
ü
ü
EVP, Legal, General Council
ü
ü
EVP, Business Development
ü
EVP, Human Resources
ü
ü
EVP, Portfolio Strategy
ü
ü
EVP, Global Neurology
EVP, Pharmaceutical Operations & Technology
ü
EVP, Oncology/Rheumatology SBU
ü
SVP, U.S. Neurology
ü
VP, Manufacturing
ü
Chief Technical Officer, Technical Development
ü
VP, Global Supply Chain
ü
VP, Global Engineering
ü
SVP, Neurology Research & Development
ü
VP, Chief Medical Officer
ü
VP, Global Drug Safety & Risk Management
ü
SVP, Immunology Research & Development
ü
VP, Cardio & Emerging T&A
ü
EVP, Portfolio Strategy
ü
SVP, CAO, Corporate Controller
ü
ü
VP, Treasury
ü
Director, Finance
ü
VP, Business Planning
ü
EVP, Human Resources
ü
ü
VP, Compensation, Benefits & Systems
ü
VP, Organization Effectiveness, Leadership Develop
ü
EVP, Legal, General Council
ü
ü
VP, Chief Corporation Council
ü
VP, Legal
ü
| | Introductions |
| | Agenda showing sections, with names and titles of presenters |
| | Company Overview |
| | Key company investment highlights | ||
| | Organization Charts | ||
| | 3-5 pages overview slides | ||
| | Summary of 2007-2010 strategy goals |
| | Commercial Business Overview |
| | Avonex | ||
| | Rituxan | ||
| | Tysabri | ||
| | Customer service capabilities |
| | R&D |
| | Neurology | ||
| | Immunology | ||
| | Oncology | ||
| | New Specialty Markets |
| | Process Capabilities and Operations |
| | Process Capabilities | ||
| | Manufacturing capabilities, capacity, flexibility |
| | Legal and Intellectual Property | |
| | Financial review |
| | Overview of systems and controls | ||
| | Historical Financials |
| | 3-year historical financials | ||
| | Discussion of historical trends by line item (COGS, R&D, S&M, G&A) |
| | Financial Projections |
| | Financial growth drivers | ||
| | 2007-2017 financial projections with revenue by product | ||
| | Key assumptions underlying 2007-2017 forecasts | ||
| | Capex, working capital and other cash flow items | ||
| | R&D and SG&A standalone leverage assumptions |
| | Resources |
| | HR headcount by function | ||
| | R&D resources (FTEs by function, R&D expenses by category) | ||
| | S&M/G&A (FTEs by function, expenses by category) |
| | Conclusions |
| | Overview of activities to date | |
| | Overview of Round II of process |
| | Draft presentation schedule | ||
| | REDACTED |
| | Participants | ||
| | Draft outline of management presentation | ||
| | Break-out session overview | ||
| | REDACTED |
| | October 12, 2007: Public announcement of process | |
| | All identified buyers contacted and initial feedback on interest received | |
| | CA process completed | |
| | First round data room open and access granted as CAs are signed | |
| | First round 2 hour calls week of October 29 th |
| | Round II presentations to be scheduled for week of the November 12th |
| | Management presentation rehearsal scheduled for November 12th | ||
| | Break-out sessions post management presentation | ||
| | Location: Hilton Boston Financial District, 89 Broad Street |
| | Buyer diligence requests will come initially to the bankers |
| | Diligence request log created for all requests |
|
Management Presentation
|
8:00 am 11:30 am | |
|
Q&A Period
|
11:30 am 12:00 pm | |
|
Lunch
|
12:00 pm 1:00 pm | |
|
Break-out Sessions
|
1:00 pm 4:00 pm | |
|
Break-out Session 1
|
||
|
Neurology Commercial
|
1:00 pm 2:30 pm | |
|
Oncology / RA Commercial
|
2:30 pm 4:00 pm | |
|
Break-out Session 2
|
||
|
Pharmaceutical Operations
|
2:30 pm 4:00 pm | |
|
Break-out Session 3
|
||
|
R&D Overview
|
1:00 pm 3:30 pm | |
|
Neurology
|
||
|
Immunology / Cardio / Hemophilia
|
||
|
Oncology
|
||
|
Break-out Session 4
|
||
|
Finance
|
1:00 pm 3:00 pm | |
|
Break-out Session 5
|
||
|
Human Resources
|
1:00 pm 2:00 pm | |
|
Break-out Session 6
|
||
|
Legal / IP
|
1:00 pm 2:00 pm |
| Management | Preparation | |||||||||
| Name | Position | Presentation | Break-out | Point-Person | ||||||
|
Management Presentation
|
President, CEO | ü | ||||||||
|
|
President, R&D | ü | ||||||||
|
|
EVP, Finance & CFO | ü | ü | |||||||
|
|
EVP, Legal, General Council | ü | ü | |||||||
|
REDACTED
|
EVP, Business Development | ü | ||||||||
|
|
EVP, Human Resources | ü | ü | |||||||
|
|
EVP, Portfolio Strategy | ü | ü | |||||||
|
|
EVP, Pharmaceutical Operations & Technology | ü | ü | |||||||
|
|
EVP, Oncology/Rheumatology SBU | ü | ü | |||||||
|
|
SVP, Neurology Research & Development | ü | ü | |||||||
|
|
SVP, Immunology Research & Development | ü | ü | |||||||
|
Neurology Commercial
|
EVP, Global Neurology | ü | ||||||||
|
|
EVP, Pharmaceutical Operations & Technology | ü | ü | |||||||
|
|
SVP, U.S. Neurology | ü | ||||||||
|
Oncology / RA Commercial
|
EVP, Oncology/Rheumatology SBU | ü | ü | |||||||
|
Pharmaceutical Operations
|
VP, Manufacturing | ü | ||||||||
|
|
EVP, Pharmaceutical Operations & Technology | ü | ü | |||||||
|
|
Chief Technical Officer, Technical Development | ü | ||||||||
|
|
VP, Global Supply Chain | ü | ||||||||
|
|
VP, Global Engineering | ü | ||||||||
| Management | Preparation | |||||||||
| Name | Position | Presentation | Break-out | Point-Person | ||||||
|
R&D Neurology
|
SVP, Neurology Research & Development | ü | ü | |||||||
|
|
REDACTED | VP, Chief Medical Officer | ü | |||||||
|
|
VP, Global Drug Safety & Risk Management | ü | ||||||||
|
R&D Immunology / Cardio / Hemophilia
|
SVP, Immunology Research & Development | ü | ü | |||||||
|
|
VP, Cardio & Emerging T&A | ü | ||||||||
|
R&D Oncology
|
EVP, Portfolio Strategy | ü | ü | |||||||
|
|
VP, Oncology Medical Officer | ü | ||||||||
|
Finance
|
EVP, Finance & CFO | ü | ü | |||||||
|
|
SVP, CAO, Corporate Controller | ü | ||||||||
|
|
VP, Treasury | ü | ||||||||
|
|
Director, Finance | ü | ||||||||
|
|
VP, Business Planning | ü | ||||||||
|
Human Resources
|
EVP, Human Resources | ü | ü | |||||||
|
|
VP, Compensation, Benefits & Systems | ü | ||||||||
|
|
VP, Organization Effectiveness, Leadership Develop | ü | ||||||||
|
Legal / IP
|
EVP, Legal, General Counsel | ü | ü | |||||||
|
|
VP, Chief Corporation Counsel | ü | ||||||||
|
|
VP, Chief IP Counsel | ü | ||||||||
| Topic | Presenter | |||
|
Introduction
|
||||
|
Commercial Business Overview
|
||||
|
Avonex
|
||||
|
Tysabri
|
||||
|
Commercial Capabilities Neurology
|
||||
|
Rituxan (Oncology / RA)
|
REDACTED | |||
|
R&D
|
||||
|
Neurology R&D
|
||||
|
Immunology, Cardiovascular, and New Markets R&D
|
||||
|
Oncology and Syntonix R&D
|
||||
|
Process Science, Manufacturing & Facilities
|
||||
|
Finance
|
||||
7
| Participants | Time | Topic | Comments | |||||
|
Session 1: Commercial
|
||||||||
|
|
90 | Neuro Commercial | REDACTED | |||||
|
|
90 | Onco / RA Commercial | ||||||
| Session 2: Pharmaceutical Operations | ||||||||
|
|
90 | Pharmaceutical Operations | ||||||
| Session 3: Research and Development | ||||||||
|
|
50 | R&D Neuro | ||||||
|
|
50 | R&D Immuno / Cardio / Hemophilia | ||||||
|
|
50 | R&D Oncology | ||||||
| Session 4: Finance | ||||||||
|
|
120 | Finance | ||||||
| Session 5: Human Resources | ||||||||
|
|
60 | HR | ||||||
| Session 6: Legal | ||||||||
|
|
60 | Legal | ||||||
8
| § | October 12, 2007: Public announcement of process | |
| § | All identified buyers contacted and initial feedback on interest received | |
| § | First round data room open and access granted | |
| § | First round 2 hour calls completed | |
| § | First round bids due November 6 th | |
| § | Board call on November 8 th to review bids | |
| § | Second round data room scheduled to be open November 9 th |
| Scenario I | Scenario II | Scenario III | ||||||||||
| Attractive Bids | Inconclusive Bids | No Bids | ||||||||||
|
Considerations
|
§ | Signals strong interest in Bellona | § | Key issue: Do the bids warrant continuing the process? | § | Bidders could either not submit a bid or signal to bankers that bids would be below market price | ||||||
|
|
||||||||||||
|
|
§ | Potential transaction value higher than standalone valuation range | § | How credible are bids? | § | Potential transaction value lower than standalone valuation range | ||||||
|
|
||||||||||||
|
|
§ | How credible are bids? | § | Are bidders likely to bid at same level or go higher after further diligence? | ||||||||
|
|
||||||||||||
|
|
§ | Are bidders likely to bid at same level or go higher after further diligence? | § | Potential signals to buyer(s) by inviting into second round? | ||||||||
|
|
||||||||||||
|
|
§ | What level of approvals has been received? | § | How will investors react? | ||||||||
|
|
||||||||||||
|
Next Steps
|
§ | Review bids with Board | § | What level of approvals has been received? | § | Review bids with Board | ||||||
|
|
||||||||||||
|
|
§ | Continue current process timeline | § | Review bids with Board | § | Publicly announce termination of process | ||||||
|
|
||||||||||||
|
|
§ | Bidder(s) will be invited into the second round | § | If Board decides to continue, see current process timeline | § | Plan B strategy | ||||||
|
|
||||||||||||
|
|
§ | If Board decides to terminate process, see Plan B | ||||||||||
|
|
||||||||||||
|
|
§ | Bidder(s) will be invited into the second round | ||||||||||
| Sunday | Monday | Tuesday | Wednesday | Thursday | Friday | Saturday | ||||||
|
December
|
||||||||||||
|
|
||||||||||||
|
|
3 | 4 | 5 | 6 | 7 | |||||||
|
¬
Process Diligence Requests
®
|
||||||||||||
|
|
||||||||||||
|
|
10 | 11 | 12 | 13 | 14 | 15 | ||||||
|
|
Final Bids Due | Board Call to review | ||||||||||
|
|
bids (TBD) | |||||||||||
|
|
||||||||||||
|
16
|
17 | 18 | 19 | 20 | 21 | |||||||
|
Execute merger
|
Announce | |||||||||||
|
agreements
|
Transaction | |||||||||||
|
|
||||||||||||
|
|
24 | 25 | 26 | 27 | 28 | |||||||
|
|
Deadline to submit | |||||||||||
|
|
proposals for inclusion | |||||||||||
|
|
in 2008 proxy | |||||||||||
|
|
||||||||||||
|
|
31 | |||||||||||