defa14a
UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
SCHEDULE 14A
PROXY STATEMENT PURSUANT TO SECTION 14(a) OF
THE SECURITIES EXCHANGE ACT OF 1934
Filed by the Registrant þ
Filed by a Party other than the Registrant o
Check the appropriate box:
o Preliminary Proxy Statement
o Confidential, for Use of the Commission Only (as permitted by Rule 14a-6(e)(2))
o Definitive Proxy Statement
o Definitive Additional Materials
þ Soliciting Material Pursuant to § 240.14a-12
BIOGEN IDEC INC.
(Name of Registrant as Specified In Its Charter)
N.A.
(Name of Person(s) Filing Proxy Statement, if other than the Registrant)
Payment of Filing Fee (Check the appropriate box):
þ No fee required.
o Fee computed on table below per Exchange Act Rules 14a-6(i)(1) and 0-11.
| |
(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: |
o Fee paid previously with preliminary materials.
| o |
|
Check box if any part of the fee is offset as provided by Exchange Act Rule 0-11(a)(2) and identify the
filing for which the offsetting fee was paid previously. Identify the previous filing by registration
statement number, or the Form or Schedule and the date of its filing. |
| |
(1) |
|
Amount Previously Paid: |
| |
| |
(2) |
|
Form, Schedule or Registration Statement No.: |
| |
| |
(3) |
|
Filing Party: |
| |
| |
(4) |
|
Date Filed: |
|
Biogen Idec
R&D Strategy
Cecil B. Pickett, PhD
President, Research & Development
March 25, 2009
|
|
Forward Looking Statements and Important Information
This presentation includes forward-looking statements about:
- estimates of the market potential for our product candidates
- our expected filings with regulatory agencies
- the anticipated development and timing of programs in our clinical pipeline
Each forward-looking statement is subject to risks and uncertainties that could cause actual results to differ materially from those
that we express or imply, including the uncertainty of success in commercializing our products, the occurrence of adverse safety
events with our products, competitive pressures, our dependence on collaborations over which we may not always have full
control, our ability to attract and retain qualified personnel, our ability to protect our intellectual property rights and the cost of
doing so, product liability claims, and the other risks and uncertainties that are described in Item 1.A. Risk Factors in our annual
report on Form 10-K and in other reports we file with the SEC.
These forward-looking statements speak only as of the date of this presentation, and we do not undertake any obligation to
publicly update any forward-looking statements, whether as a result of new information, future events, or otherwise.
Biogen Idec and its directors, executive officers and other members of its management and employees may be deemed to be
participants in the solicitation of proxies from the stockholders of Biogen Idec in connection with the Company's 2009 annual
meeting of stockholders. Information concerning the interests of participants in the solicitation of proxies will be included in any
proxy statement filed by Biogen Idec in connection with the Company's 2009 annual meeting of stockholders.
In addition, Biogen Idec files annual, quarterly and special reports with the Securities and Exchange Commission (the "SEC").
The proxy statements and other reports, when available, can be obtained free of charge at the SEC's web site at www.sec.gov or
from Biogen Idec at www.biogenidec.com. Biogen Idec stockholders are advised to read carefully any proxy statement filed in
connection with the Company's 2009 annual meeting of stockholders when it becomes available before making any voting or
investment decision. The Company's proxy statement will also be available for free by writing to Biogen Idec Inc., 14 Cambridge
Center, Cambridge, MA 02142. In addition, copies of the proxy materials may be requested from our proxy solicitor, Innisfree
M&A Incorporated, by toll-free telephone at (877) 750-5836 or by e-mail at info@innisfreema.com.
|
|
Biogen Idec R&D Strengths
Strong R&D fundamentals
World class biotherapeutic discovery and development organization
Focused drug discovery and development efforts
Neurology
Immunology
Oncology
Cardiology
Strong link between discovery research, clinical development, and
strategic business units
Proven track record of discovering and developing innovative
molecules
Extensive biologic manufacturing expertise
|
|
R&D Strategy
Preclinical
Proof-of-
Concept
Registration
& Filing
First-in-Human
5 programs
13 programs
7 programs
20 programs
Focus on novel therapeutics
to address areas of high
unmet medical need
Internal discoveries and in-
licensing opportunities
First-in-Class molecules as
well as Best-in-Class
molecules
Biologics and small
molecules
|
|
Goal of Strong Growth in Registrational Programs
BG-12 MS
Galiximab
Lumiliximab
Lixivaptan -
Hyponatremia
Ocrelizumab RA
BG-12 MS
Galiximab
Lumiliximab
Lixivaptan -
Hyponatremia
Ocrelizumab RA
ADENTRI(r) IV
BG-12 MS
Galiximab
Lumiliximab
Lixivaptan -
Hyponatremia
Ocrelizumab RA
ADENTRI IV
PEG-IFN
BG-12 MS
Galiximab
Lumiliximab
Lixivaptan -
Hyponatremia
Ocrelizumab RA
ADENTRI IV
PEG-IFN
Lixivaptan - HF
Daclizumab
Registration Programs
Q108 1H 08 Q308 2H 08 Q109 1H 09 Q309 2H 09
Ph 1 5 5 7 6 6 5 5 5
Ph 2 13 13 12 14 15 15 12 12
Ph 3 4 5 5 6 9 7 11 9
PMC 3 3 3 3 3 3 3 3
Label 25 25 27 30 33 33 31 32
|
|
Independent Assessment by Moody's -
Highest Quality Late Stage Pipeline
Moody's Investors Service research
Issuer Scorecard: Large U.S.
Pharmaceutical Companies published
February 2009
Most recent rating methodology mapping
for 12 large U.S.-based pharmaceutical
and biotech companies
Ranking of the 12 companies from
strongest to weakest on several important
criteria
Biogen Idec ranked
Highest on late-stage pipeline quality
Top third on pipeline diversity, within the
most diverse category
Additional details at www.moodys.com
Table 2
Late-Stage Pipeline Quality
Biogen Idec (Baa3)
54.3%
Allergan (A3)
31.8%
Schering-Plough (Baa1)
27.7%
J&J (Aaa) / Pharma Only**
27.5%
Amgen (A3)
23.8%
Genentech (A1*)
21.0%
Wyeth (A3*)
20.1%
Eli Lilly & Company (A1)
18.8%
Bristol-Myers Squibb (A2)
16.8%
Merck & Co., Inc. (Aa3)
16.5%
Abbott (A1) / Pharma Only**
14.2%
J&J (Aaa) / Total Company**
11.4%
Abbott (A1) / Total Company**
11.4%
Pfizer (Aa1*)
10.0%
= Highest score (> 30%)
= Lowest score (< 15%)
* Ratings under review
** Ratios shown on both bases for J&J and Abbott
|
|
H2 2007
H1 2008
H2 2008
Daclizumab in RRMS - Ph2 (CHOICE)
Baminercept in RA - Ph2a
RITUXAN in SLE - Ph2/3
RITUXAN(r) in DMARD-IR RA - Ph3
RITUXAN in PPMS - Ph3
BIIB14 in PD - Ph2a
Hsp90i in GIST - Ph2a
Volociximab in Ovarian - Ph2
RITUXAN in DMARD-naive RA - Ph3
RITUXAN in CLL - Ph3
Positive Readout
Negative Readout
Baminercept in RA - Ph2b
Potential Readouts 2009 & 2010
AVONEX in UC - Ph2
CDP323 in RRMS - Ph2
Daclizumab in RRMS - Ph2 (SELECT)
Long Acting rFactor IX in Hemophilia B
- - Ph1/2
Lumiliximab in CLL - Ph2 portion of
Ph2/3
Ocrelizumab in RRMS - Ph2
Ocrelizumab in RA - Ph3
Delivering Data Readouts and Decision Points
RITUXAN in LN - Ph3
H1 2009
CLL - chronic lymphocytic leukemia; RRMS - relapsing remitting
multiple sclerosis; RA - rheumatoid arthritis; UC - ulcerative colitis
|
|
14
Patents and Publications
Recent Patents
5,763 Total Biogen Idec Patents
Total Issued WW (approx.)
Total Pending WW (approx.)
2,877
2,886
2008 Publications
89 Peer Reviewed
Publications in 2008
Clinical Publications 38
Immunology 34
Neurology 22
Oncology 13
Cardiovascular 12
Hematology 7
0
100
200
300
400
500
600
700
800
900
2006
2007
2008
Patents Issued
Applications
Filed
|
|
R&D Organization Summary
Outstanding people at all levels in the R&D Organization
Robust pipeline with important compounds at all stages
of development
World-class expertise in discovery and development of
biologics
Focus on executing clinical trials
Continue developing compounds in registrational programs
Move earlier programs rapidly to proof-of-concept
|
|
Biogen Idec
Pipeline Summary
Cecil B. Pickett, PhD
President, Research & Development
March 25, 2009
|
|
Robust Pipeline - Late, Early, Discovery
Product pipeline significantly strengthened over past three years
More than 20 programs added to the clinical pipeline or advanced to next clinical
step since the start of 2007
More than ten molecules accessed via business development strategy
60 clinical trials ongoing
More than four fold increase in patients enrolled in clinical trials since 2007
15 indications across neurology, oncology, immunology, cardiopulmonary and
hemophilia
Seven programs currently in registrational trials and filing
20 programs in Phase 2 or beyond
More than 35 preclinical and discovery research programs
|
|
Neurology
Oncology
Cardiopulmonary & Emerging Areas
Immunology
14
AVONEX
TYSABRI
BG-12
Daclizumab
Multiple sclerosis
Multiple sclerosis
Multiple sclerosis
Multiple sclerosis
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
RITUXAN
FUMADERM(r)
TYSABRI
RITUXAN
Ocrelizumab
Rheumatoid arthritis
Psoriasis
Crohn's disease
ANCA-Associated Vasculitis
Rheumatoid arthritis
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
RITUXAN
Galiximab
Lumiliximab
NHL & CLL (Ph. 3)
NHL
CLL
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
Lixivaptan
ADENTRI(r) (IV)
Heart Failure / Hyponatremia
Acute Heart Failure
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
January 2007 Pipeline
2007 and 2008 Progress
Late Stage Pipeline
Seven programs
in registrational
trials and filing
|
|
Oncology
Cardiopulmonary & Emerging Areas
Immunology
Neurology
14
Ocrelizumab
CDP323
BIIB014
PEGylated-IFN^1a
Neublastin
Anti-LINGO-1
S1P agonist
Multiple sclerosis
Multiple sclerosis
Parkinson's
Multiple sclerosis
Pain
MS
MS
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
AVONEX
BG-12
Anti-TWEAK
Anti-CD40L
Ulcerative Colitis
Rheumatoid arthritis
RA
SLE
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
Volociximab
HSP90 Inhibitor
Anti-Cripto-DM4
Anti-IGF-1R
TYSABRI
RAF Inhibitor
Anti-Fn14
Solid tumors
Solid tumors
Solid
Solid
Multiple Myeloma
Solid
Solid
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
ADENTRI (oral)
Long Acting rFactor IX
Long Acting rFactor VIII
Chronic Heart Failure
Hemophilia B
Hem A
Pre-Clinical
Phase 1
Phase 2
Phase 3
Market
Early Stage Pipeline
BART
AD
Anti-FcRn
Inflam
January 2007 Pipeline
2007 and 2008 Progress
GA101
NHL/CLL
20 Programs
in Phase 2
and Beyond
|
|
Biogen Idec Research & Development Day
March 25, 2009
|