The Zacks Analyst Blog Highlights: Gilead Sciences, Bristol-Myers Squibb, Inhibitex, Vertex Pharmaceuticals & Merck - Press R..
20 January 2012 - 7:30PM
Zacks
For Immediate Release
Chicago, IL – January 20, 2012 – Zacks.com announces the list of
stocks featured in the Analyst Blog. Every day the Zacks Equity
Research analysts discuss the latest news and events impacting
stocks and the financial markets. Stocks recently featured in the
blog include Gilead Sciences,
Inc. ( GILD), Bristol-Myers Squibb
Company ( BMY), Inhibitex, Inc. ( INHX),
Vertex Pharmaceuticals ( VRTX) and
Merck ( MRK).
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Here are highlights from Thursday’s Analyst
Blog:
Gilead Completes
Pharmasset Buy
Gilead Sciences, Inc. ( GILD) announced
recently that it has completed its previously announced agreement
to buy Pharmasset, Inc, a maker of drugs for the treatment of
chronic hepatitis C virus (HCV), for approximately $11.2 billion.
Gilead paid $137 for each share of Pharmasset. Gilead had entered
into a definitive agreement to buy Pharmasset in November last
year. The deal is expected to be dilutive through 2014 and
accretive to earnings from 2015 onwards.
Pharmasset currently has three pipeline candidates in various
stages of development for the treatment of HCV. The lead candidate
is PSI-7977 which is undergoing two late-stage trials in patients
with HCV of genotype II and III. Both studies are studying PSI-7977
in combination with standard of care ribavirin. PSI-7977 is also
being studied in a mid-stage trial in combination studies in HCV
patients infected with genotype I virus. The candidate is expected
to move into late-stage trials in the second half of 2012. The
second candidate PSI-938 is being studied as a monotherapy and also
in combination with PSI-7977 in HCV patients of all viral
genotypes. The third candidate Mericitabine (RG7128) is in
mid-stage trials.
These pipeline candidates are expected to synergize well with
Gilead’s HCV portfolio. Gilead is hoping to build one of the
largest HCV pipelines and is currently evaluating seven molecules
for the treatment of HCV. Gilead is also studying drug combinations
to develop all oral regimens aimed to reduce treatment duration to
12-16 weeks and spare the use of the current standard-of-care
pegylated interferon associated with some serious side effects.
Three mid-stage trials are ongoing to develop all oral interferon
free regimens, data from which are expected in 2012 and early 2013.
Gilead believes Pharmasset’s candidates, particularly PSI-7977,
have the potential to be combined with Gilead’s HCV pipeline
candidates resulting in multiple all-oral interferon-free
regimens.
We note that other major companies are also targeting the HCV
market. Early this month pharma giant Bristol-Myers Squibb
Company ( BMY) announced a $2.5 billion deal to acquire
biopharmaceutical company Inhibitex, Inc. ( INHX).
The deal is expected to bolster Bristol-Myers’ pipeline
significantly with the major attraction being HCV candidate INX-189
(phase II). We believe INX-189 could pose strong competition to
Pharmasset’s PSI-7977, once both drugs are approved.
The above deals clearly convey the increasing importance of the
HCV market. The market is characterized by a significant unmet
need. It is estimated that approximately 170 million people suffer
from HCV infection across the world. However, the treated
population is much lower. This leaves the field open for new
treatments.
Secondly, the current standard of care comes with several side
effects which make it difficult for patients to remain on
treatment. A 48-week course of both peg-interferon (peg-INF -
weekly injections) and ribavirin (RBV - oral drug) are the standard
treatment for genotype I HCV infection.
Vertex Pharmaceuticals’ ( VRTX) Incivek and
Merck’s ( MRK) Victrelis (both approved last year
in the US) are examples of the changing treatment regimen in the
HCV market. Both are protease inhibitors which when added to the
standard of care not only reduce the treatment period but also
improve the treatment outcome. These factors have made the HCV
market an attractive commercial opportunity for pharma and biotech
companies.
In a separate development, Gilead recently announced that the US
Food & Drug Administration has approved its marketed drug
Viread for combination use in the treatment of HIV in children
(2-12 years). Moreover, the FDA also approved three lower strength
tablets of the medicine for children in the age group of 6-12
years. In addition, an oral powder formulation of the drug was also
approved for children in the age group of 2-5 years. Viread was
until now approved for use in adults and adolescents for the
treatment of HIV and chronic hepatitis B, a serious liver disease
caused by the hepatitis B virus (HBV).
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BRISTOL-MYERS (BMY): Free Stock Analysis Report
GILEAD SCIENCES (GILD): Free Stock Analysis Report
INHIBITEX INC (INHX): Free Stock Analysis Report
MERCK & CO INC (MRK): Free Stock Analysis Report
VERTEX PHARM (VRTX): Free Stock Analysis Report
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