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Profile
Pricing data through 30 Dec 2010 InterMune, Inc. is a biotech company focused on developing
and commercializing innovative therapies in pulmonology
and hepatology. The company’s sole approved product is
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company profile, Morningstar Actimmune which is approved by the FDA only for the
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treatment of two rare congenital disorders: CGD and severe,
malignant osteopetrosis. Actimmune is also approved for
For information about our full analyst
coverage, please contact: these indications by the health authorities in numerous
Morningstar Equity Research other countries. CGD is a life-threatening congenital
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disorder that causes patients, mainly children, to be
vulnerable to severe, recurrent bacterial and fungal
Contents infections. This results in frequent and prolonged
hospitalizations and commonly results in death. Severe,
Company Profile 1
malignant osteopetrosis is a life-threatening, congenital
Company Data 2
disorder that mainly affects children. This disease results
Management & Ownership 3
in increased susceptibility to infection and an overgrowth
Industry Focus 4
of bony structures that might lead to blindness and/or
deafness. It has an advanced-stage development pipeline
in the pulmonology area and a research and development-
stage pipeline in the hepatology area. In pulmonology, it is
developing a single therapy for the treatment of IPF. IPF is
a fatal disease characterized by progressive scarring, or
fibrosis, of the lungs, which leads to the deterioration and
destruction of lung function. In hepatology, it is developing
product candidates to provide expanded treatment options
for patients suffering from HCV infection.
©2009 Morningstar. All Rights Reserved. Unless otherwise provided in a separate agreement, you may use this report only in the country in which its original distributor is based. Data as originally reported. The information contained herein is not Page 1 of 5
represented or warranted to be accurate, correct, complete, or timely. This report is for information purposes only, and should not be considered a solicitation to buy or sell any security. Redistribution is prohibited without written permission. To
order reprints, call +1 312-696-6100. To license the research, call +1 312-696-6869.
Morningstar StockResearch
Morningstar®Equity Data Sheet Pricing data thru Dec. 30, 2010 Rating updated as of Dec. 30, 2010 Fiscal year-end: December
InterMune, Inc. ITMN Sales USD Mil Mkt Cap USD Mil Industry
24 2,068 Biotechnology
Sector
Health Care
© 2010 Morningstar. All Rights Reserved. Unless otherwise provided in a separate agreement, you may use this report only in the country in which its original distributor is based. Data as originally reported. ®
The information contained herein is not represented or warranted to be accurate, correct, complete, or timely. This report is for information purposes only, and should not be considered a solicitation to buy or sell any security.
Redistribution is prohibited without written permission. To order reprints, call +1 312-696-6100. To license the research, call +1 312-696-6869.
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*Report date represents the date on which the owner's common shares held was audited.
Fund Ownership
Morningstar % of Shares % of Fund Change
Top Owners Rating Held Assets (k) Portfolio Date
Concentrated Holders
Institutional Transactions
Shares
Morningstar % of Shares % of Fund Bought/
Top 5 Buyers Rating Held Assets Sold (k) Portfolio Date
T. Rowe Price Health Sciences QQQQ 0.84 0.27 168 30 Sep 2010
T. Rowe Price New Horizons QQQQ 0.66 0.08 162 30 Sep 2010
Pictet-Biotech-P dy USD QQQ 3.52 1.87 143 30 Sep 2010
TFS Market Neutral QQQQQ 0.10 0.16 55 31 Jul 2010
Managed Account Global SmallCap QQQQQ 0.04 0.21 25 31 Jul 2010
Top 5 Sellers
First Trust NYSE Arca Biotech Index QQQQQ 1.05 4.54 -148 31 Oct 2010
Oppenheimer Global A QQQ 2.00 0.13 -133 30 Jun 2010
BlackRock Global SmallCap Inv A QQQQ 0.17 0.12 -101 30 Sep 2010
Dexia Equties L Biotechnology I USD Acc 0.13 0.77 -97 31 Oct 2010
©2009 Morningstar. All Rights Reserved. Unless otherwise provided in a separate agreement, you may use this report only in the country in which its original distributor is based. Data as originally reported. The information contained herein is not Page 3 of 5
represented or warranted to be accurate, correct, complete, or timely. This report is for information purposes only, and should not be considered a solicitation to buy or sell any security. Redistribution is prohibited without written permission. To
order reprints, call +1 312-696-6100. To license the research, call +1 312-696-6869.
Morningstar Equity Research
therapies are about The meteoric rise in the overnight share prices of modern- Vertex's chief rival, Merck MRK , is developing a protease
to face judgment day Lazuruses like Vanda Pharmaceuticals VNDA and, inhibitor of its own. We think telaprevir's slightly superior
most recently, Orexigen Therapeutics have become the stuff efficacy and convenience profile should give it an advantage
day. of biotech legends. However, it is important to remember with prescribers. However, Vertex has no commercialization
that many more biotechs crash and burn than make it big. experience, and Merck's established salesforce and ability
to package the drug with the current standard of care should
More often than not, biotech shareholders are left empty- help even the commercialization playing field. Vertex ranked
handed. Below we highlight three development-stage number 1 on our 2010 biotech takeout list, and we continue
biotechs with highly anticipated new therapies that are to believe the firm would benefit from the sales know-how
about to face judgment days of their own. of a larger pharma player like current partner Johnson
Johnson JNJ . The stock currently trades at a 25% discount
to our fair value estimate, providing an attractive entry point
for investors with a stomach for risk.
Vertex's Telaprevir Aims to Revolutionize HCV
While Vertex also has a late-stage cystic fibrosis candidate
and compounds in earlier-stage development, telaprevir
remains the focus of investor excitement and the primary
value driver of the firm. We give the drug a 70% chance of
approval, 10% higher than our average Phase III drug. If
telaprevir succeeds in clinching approval, our fair value
estimate would rise to at least $50 (not including a takeout
premium). With a drug on the market, we think Vertex could
see profitability by 2013. However, a great deal is still
unknown about telaprevir's remaining late-stage data and
commercialization plans. If telaprevir takes longer than
expected or requires more resources to get to market, our
fair value estimate would fall to under $30.
©2009 Morningstar. All Rights Reserved. Unless otherwise provided in a separate agreement, you may use this report only in the country in which its original distributor is based. Data as originally reported. The information contained herein is not Page 4 of 5
represented or warranted to be accurate, correct, complete, or timely. This report is for information purposes only, and should not be considered a solicitation to buy or sell any security. Redistribution is prohibited without written permission. To
order reprints, call +1 312-696-6100. To license the research, call +1 312-696-6869.
Morningstar Equity Research
Dearth of New Lupus Drugs disease management to injectable insulin. In trials, Afrezza
Human Genome Sciences' HGSI lupus drug Benlysta achieved comparable levels of overall glucose control while
could become the first lupus medication to gain approval in also demonstrating a lower risk of hypoglycemia and weight
over five decades. The first-in-class drug has demonstrated gain than currently available products. Despite these
promising Phase III data in seropositive patients--those with advantages, MannKind received a complete response letter
an autoantibody present in their bloodstream. While the from the FDA asking for more data earlier this year. The good
drug has had issues demonstrating significant long-term news for MannKind was that the FDA did not require
efficacy, we think Benlysta could be a unique candidate to additional Phase III trials, which likely would have been
use in combination with the standard of care. With no direct prohibitive for the unprofitable biotech.
treatment for lupus, any improvement to the current steroid-
based treatment could make the drug very attractive, and MannKind expects to hear back from the FDA by Dec. 29,
we think Benlysta could turn into a blockbuster drug for the and we think there is a good chance Afrezza will be approved
firm. Human Genome received a favorable advisory panel (we assign Afrezza an 85% chance of approval based on
vote for Benlysta last month, with members voting 13 to 2 strong efficacy data and a clean safety record thus far).
in favor of recommending approval and 14 to 1 that the However, MannKind will face an uphill battle in its attempt
drug's safety profile was sufficient for approval. While the to turn the product into a commercial hit. Afrezza's
FDA has recently delayed its target decision date to March predecessor in the inhaled insulin class, Pfizer and Nektar's
10, 2011, we think the drug could still launch by mid-2011. Exubera, was removed from the market in 2007 after
generating disappointing sales and being linked to a
Human Genome has a robust pipeline and many drugs in potential risk of lung cancer in former smokers. Although
clinical trials. If one product fails, the firm has other Afrezza's clinical trials have yet to produce any red flags,
development options. However, much of the firm's long-term we think Exubera's failings will haunt MannKind's efforts
value remains tied to Benlysta. If the firm's share of Benlysta to win favor among prescribers. MannKind also trades at a
sales could surpass $1.5 billion by 2019, we would raise our discount to our fair value estimate, but we think Afrezza's
fair value estimate to $27 per share. If Benlysta does not fate represents more of a binary outcome for the firm, unlike
gain approval, Human Genome would be left to rely on Vertex's telaprevir or Human Genome's Benlysta. The firm
earlier-stage pipeline candidates and two Phase III carries a very high uncertainty rating and should be regarded
candidates that we believe have only modest commercial as a speculative investment.
potential. Our fair value estimate in this case would fall to
$5 per share. While we think the firm is fairly valued at
current trading levels, Human Genome represents another
key takeout opportunity, in our opinion. The company ranked
number 3 on our 2010 list of biotech takeout targets, and
we think an acquisitor like current partner GlaxoSmithKline
GSK would make strategic sense.
©2009 Morningstar. All Rights Reserved. Unless otherwise provided in a separate agreement, you may use this report only in the country in which its original distributor is based. Data as originally reported. The information contained herein is not Page 5 of 5
represented or warranted to be accurate, correct, complete, or timely. This report is for information purposes only, and should not be considered a solicitation to buy or sell any security. Redistribution is prohibited without written permission. To
order reprints, call +1 312-696-6100. To license the research, call +1 312-696-6869.