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SECURITY: JNJ (Common)
EXCHANGE: New York Stock Exchange CURRENCY: US Dollar
Johnson & Johnson,
employing approximately 110,300 people worldwide, is engaged in the manufacture
and sale of a broad range of products in the health care field in many
countries of the world. Johnson & Johnson's primary interest, both
historically and currently, has been in products related to health and
well-being. Johnson & Johnson was organized in the State of New Jersey
in 1887.
Fondé en 1887,
Johnson & Johnson est l'un des premiers groupes pharmaceutiques mondiaux.
- produits pharmaceutiques
. Johnson & Johnson développe et commercialise des médicaments
destinés au traitement des pathologies suivantes : maladies cardio-vasculaires,
oncologie, maladies gastro-intestinales, immunologie, neurologie, dermatologie,
contraception ...
- produits professionnels
. J&J développe, fabrique et commercialise des produits et équipements
médicaux destinés aux professionnels de la santé :
systèmes de diagnostics, produits orthopédiques, produits
de gynécologie, matériel chirurgical, ...
-produits de grande
consommation : médicaments OTC, nutrition, soins de la personne
(marques RoC, Neutrogena, etc.), ophtalmologie (1er producteur mondial
de lentilles de contacts avec la marque Acuvue), hygiène féminine,
soins bébé, ...
http://www.jnj.com
Johnson
& Johnson Reports 2010 Second-Quarter Results:
Sales
of $15.3 Billion Increased 0.6% Versus 2009 Second-Quarter; EPS was $1.23
Excluding Special Items, 2010 Second-Quarter EPS was $1.21, an increase
of 5.2%*
NEW
BRUNSWICK, N.J., July 20, 2010 /PRNewswire via COMTEX News Network/ --
Johnson & Johnson (NYSE: JNJ) today announced sales of $15.3 billion
for the second quarter of 2010, an increase of 0.6% as compared to the
second quarter of 2009. Operational results increased 0.1% and the positive
impact of currency was 0.5%. Domestic sales declined 2.8%, while international
sales increased 4.1%, reflecting operational growth of 3.0% and a positive
currency impact of 1.1%.
Net
earnings and diluted earnings per share for the second quarter of 2010
were $3.4 billion and $1.23, respectively. Second-quarter 2010 net earnings
included an after-tax gain of $67 million representing the net impact of
litigation matters. Excluding this special item, net earnings for the current
quarter were $3.4 billion and diluted earnings per share were $1.21, representing
increases of 5.4% and 5.2%, respectively, as compared to the same period
in 2009.*
The
Company updated its earnings guidance for full-year 2010 to $4.65 - $4.75
per share, which excludes the impact of special items. The Company's guidance
now reflects the impact of the voluntary recalls announced earlier this
year of certain over-the-counter medicines and the suspension of manufacturing
at the McNeil Consumer Healthcare facility in Fort Washington, Pa., as
well as unfavorable changes in foreign currency exchange rates.
"Our
second-quarter results include strong growth in a number of our recently
launched products which contributed to solid earnings," said William C.
Weldon, Chairman and Chief Executive Officer. "Remedial actions to address
the product quality issues at McNeil Consumer Healthcare are ongoing and
of high importance. At the same time, we continue to make significant investments
in acquisitions, strategic partnerships and in advancing our pipeline,
positioning us well for future growth."
Worldwide
Consumer sales of $3.6 billion for the second quarter represented a decrease
of 5.4% versus the prior year consisting of an operational decline of 6.5%
and a positive impact from currency of 1.1%. Domestic sales decreased 14.3%;
international sales increased 1.8%, which reflected an operational decline
of 0.2% and a positive currency impact of 2.0%.....
Janssen
Pharmaceutica N.V. Announces Expansion of Licensing Agreement for Tapentadol
(NUCYNTA® /PALEXIA® /PALEXIS®)
Beerse,
Belgium (June 7, 2010) -- Janssen Pharmaceutica N.V. (Janssen) announced
today that it has expanded its licensing agreement with the Grünenthal
Group (Grünenthal) to register, manufacture and commercialize Tapentadol
in additional regions, including selected Asia Pacific, Latin American,
African, and New European countries including Turkey and Greece, under
Grünenthal's NUCYNTA® /PALEXIA® /PALEXIS® trademark for
both the immediate- and prolonged-release (IR and PR) formulations.
Johnson
& Johnson Reports 2010 First-Quarter Results:
--Sales
of $15.6 Billion Increased 4.0% Versus 2009 First Quarter; EPS was $1.62
--Excluding Special Items, 2010 First-Quarter EPS was $1.29, an increase
of 2.4%*
NEW
BRUNSWICK, N.J., April 20, 2010 /PRNewswire via COMTEX News Network/ --
Johnson & Johnson (NYSE: JNJ) today announced sales of $15.6 billion
for the first quarter of 2010, an increase of 4.0% as compared to the first
quarter of 2009. Operational results declined 0.1% and the positive impact
of currency was 4.1%. Domestic sales declined 5.0%, while international
sales increased 14.4%, reflecting operational growth of 5.5% and a positive
currency impact of 8.9%.
Net
earnings and diluted earnings per share for the first quarter of 2010 were
$4.5 billion and $1.62, respectively. First-quarter 2010 net earnings included
an after-tax gain of $910 million representing the net impact of litigation
matters. Excluding this special item, net earnings for the current quarter
were $3.6 billion and diluted earnings per share were $1.29, representing
increases of 3.1% and 2.4%, respectively, as compared to the same period
in 2009.* The Company updated its earnings guidance for full-year 2010
to $4.80 - $4.90 per share to reflect recent changes in foreign currency
exchange rates. Earnings guidance excludes the impact of special items
and now incorporates the impact of recently enacted health care reform
legislation.
"Thanks
to the outstanding efforts of our people, we were able to deliver solid
financial results," said William C. Weldon, Chairman and Chief Executive
Officer. "This was accomplished despite a major product recall and the
continued impact of patent expirations. We are well positioned for future
growth."
Worldwide
Consumer sales of $3.8 billion for the first quarter represented an increase
of 1.5% versus the prior year consisting of a decrease of 3.7% operationally
and a positive impact from currency of 5.2%. Domestic sales decreased 9.6%;
international sales increased 11.1%, which reflected an operational increase
of 1.4% and a positive currency impact of 9.7%.
Positive
contributors to operational results were NEUTROGENA(R), AVEENO(R) and LE
PETIT MARSEILLAIS(R) skin care products; ZYRTEC(R) over-the-counter allergy
treatment; international sales of LISTERINE(R) antiseptic mouthrinse; and
women's sanitary protection products. These operational sales increases
were more than offset by the impact of the previously announced recall
of selected OTC products as well as the devaluation of the Venezuelan currency.
Worldwide
Pharmaceutical sales of $5.6 billion for the first quarter represented
a decrease of 2.5% versus the prior year consisting of an operational decline
of 5.7% and a positive impact from currency of 3.2%. Domestic sales decreased
12.7%; international sales increased 15.5%, which reflected an operational
increase of 6.6% and a positive currency impact of 8.9%.
Products
with strong operational growth included REMICADE(R) (infliximab), a biologic
approved for the treatment of a number of immune mediated inflammatory
diseases; PREZISTA(R) (darunavir), a treatment for HIV; VELCADE(R) (bortezomib),
a treatment for multiple myeloma; and international sales of RISPERDAL(R)
CONSTA(R) (risperidone) Long-Acting Treatment, an antipsychotic medication.
Strong growth was also achieved from newly launched products including
STELARA(TM) (ustekinumab), a biologic approved for the treatment of moderate
to severe plaque psoriasis; and SIMPONI(TM) (golimumab), a biologic approved
to treat adults with moderate to severe rheumatoid arthritis, psoriatic
arthritis, and ankylosing spondylitis.
Sales
results of TOPAMAX(R) (topiramate), an antiepileptic and a treatment for
migraine, and RISPERDAL(R) (risperidone), an antipsychotic medication,
were negatively impacted by generic competition.
Worldwide
Medical Devices and Diagnostics sales of $6.2 billion for the first quarter
represented an increase of 12.5% versus the prior year consisting of an
operational increase of 8.1% and a positive currency impact of 4.4%. Domestic
sales increased 8.8%; international sales increased 15.9%, which reflected
an operational increase of 7.5% and a positive currency impact of 8.4%.
Primary
contributors to operational growth included Ethicon's surgical care products;
DePuy's orthopaedic joint reconstruction and sports medicine businesses;
Ethicon Endo-Surgery's minimally invasive products and Advanced Sterilization
Products' infection prevention solutions; and Ortho-Clinical Diagnostics'
professional products. This growth was partially offset by lower sales
in the Cordis franchise, reflecting continued competition in the drug-eluting
stent market.
During
the quarter, the Company filed for CE Mark in Europe for its NEVO(R) Sirolimus-Eluting
Coronary Stent, the first drug-eluting stent to utilize RES TECHNOLOGY(TM)
, eliminating the need for surface coated and permanent polymers.
Johnson
& Johnson Reports 2009 Fourth-Quarter and Full-Year Results:
--2009
Fourth-Quarter Sales of $16.6 Billion increased 9.0%; EPS was $0.79 --2009
Full-Year Sales of $61.9 Billion decreased 2.9%; Full-Year EPS was $4.40
--Excluding Special Items, 2009 Fourth-Quarter EPS was $1.02, an increase
of 8.5% --And 2009 Full-Year EPS was $4.63, an increase of 1.8%*
NEW
BRUNSWICK, N.J., Jan 26, 2010 /PRNewswire via COMTEX News Network/ -- Johnson
& Johnson today announced sales of $16.6 billion for the fourth quarter
of 2009, an increase of 9.0% as compared to the fourth quarter of 2008.
Operational growth was 4.5% and currency contributed 4.5%. Domestic sales
were up 2.6%, while international sales increased 15.6%, reflecting operational
growth of 6.4% and a positive currency impact of 9.2%. Worldwide sales
for the full-year 2009 were $61.9 billion, a decrease of 2.9% over 2008.
Operational results declined 0.3% and the negative impact of currency was
2.6%. Domestic sales declined 4.4%, while international sales declined
1.4%, reflecting operational growth of 3.9% and a negative currency impact
of 5.3%.
Net
earnings and diluted earnings per share for the fourth quarter of 2009
were $2.2 billion and $0.79 respectively. Fourth quarter 2009 net earnings
included an after-tax restructuring charge of $852 million and an after-tax
gain of $212 million representing the net impact of litigation matters.
Fourth quarter 2008 net earnings included special items related to in-process
research and development charges of $141 million with no tax benefit and
an after-tax gain of $229 million representing the net impact of litigation
matters. Excluding these special items, net earnings for the current quarter
were $2.8 billion and diluted earnings per share were $1.02, representing
increases of 8.4% and 8.5%, respectively, as compared to the same period
in 2008.*
Net
earnings and diluted earnings per share for the full-year 2009 were $12.3
billion and $4.40. Full-year 2009 net earnings included an after-tax restructuring
charge of $852 million and an after-tax gain of $212 million representing
the net impact of litigation matters. Full-year 2008 net earnings included
special items related to in-process research and development charges of
$181 million with no tax benefit and an after-tax gain of $229 million
representing the net impact of litigation matters. Excluding these special
items, net earnings for the full-year 2009 were $12.9 billion. Diluted
earnings per share for the full-year 2009 were $4.63, representing an increase
of 1.8%, as compared with the full-year in 2008.*
The
Company announced earnings guidance for full-year 2010 of $4.85 to $4.95
per share, which excludes the impact of special items.
"In
a year of tremendous challenge, we maintained our long-term focus while
delivering solid results -- a great tribute to the employees of Johnson
& Johnson," said William C. Weldon, Chairman and Chief Executive Officer.
"We made important investments in acquisitions, strategic partnerships
and launches of recently-approved innovative products while preserving
our financial flexibility to continue to invest in innovation. This positions
us well for continued leadership and growth in global health care as we
enter 2010."
Worldwide
Consumer sales of $15.8 billion for the full-year 2009 represented a decrease
of 1.6% over the prior year with operational growth of 2.0% and a negative
currency impact of 3.6%. Domestic sales decreased 1.4%; international sales
decreased 1.7%, which reflected operational growth of 4.7% and a negative
currency impact of 6.4%.
Primary
contributors to operational growth included NEUTROGENA(R), AVEENO(R) and
the Dabao skin care products; international sales of LISTERINE(R) antiseptic
mouthrinse; SPLENDA(R) No Calorie Sweetener; and sales from the acquisition
of Vania Expansion SNC. Sales growth was negatively impacted due to the
initial build of inventory by the trade related to the 2008 launch of Zyrtec.
Worldwide
Pharmaceutical sales of $22.5 billion for the full-year 2009 represented
a decrease of 8.3% versus the prior year with an operational decline of
6.1% and a negative impact from currency of 2.2%. Domestic sales decreased
12.1%; international sales decreased 2.6%, which reflected an operational
increase of 3.0% and a negative currency impact of 5.6%.
Johnson
& Johnson Reports 2009 Third-Quarter Results:
Sales
of $15.1 Billion Decreased 5.3% Versus 2008 Third Quarter
EPS
of $1.20 increased 2.6% Versus 2008 Third Quarter
NEW
BRUNSWICK, N.J., Oct 13, 2009 /PRNewswire-FirstCall via COMTEX News Network/
-- Johnson & Johnson (NYSE: JNJ) today announced sales of $15.1 billion
for the third quarter of 2009, a decrease of 5.3% as compared to the third
quarter of 2008. Operational results declined 2.8% and the negative impact
of currency was 2.5%. Domestic sales declined 8.1%, while international
sales declined 2.5%, reflecting operational growth of 2.4% and a negative
currency impact of 4.9%.
Net
earnings and diluted earnings per share for the third quarter of 2009 were
$3.3 billion and $1.20, respectively, representing increases of 1.1% and
2.6%, as compared to the same period in 2008. The Company raised its earnings
guidance for full-year 2009 to $4.54 - $4.59 per share, which excludes
the impact of special items.
"We
continue to successfully manage our broad base of businesses and deliver
solid earnings despite the impact of patent expirations and the challenges
posed by the current economic environment," said William C. Weldon, Chairman
and Chief Executive Officer. "We completed multiple acquisitions and strategic
collaborations and received several new product approvals in the quarter
that will benefit patients worldwide and drive future growth."
Worldwide
Consumer sales of $4.0 billion for the third quarter represented a decrease
of 2.7% versus the prior year with an increase of 1.1% operationally and
a negative impact from currency of 3.8%. Domestic sales decreased 4.4%;
international sales decreased 1.4%, which reflected an operational increase
of 5.2% and a negative currency impact of 6.6%.
Contributing
to operational sales growth during the quarter were sales of Dabao skin
care products; AVEENO(R) skin care products; SPLENDA(R) No Calorie Sweetener;
Le Petit Marseillais(R) beauty care products; and LISTERINE(R) antiseptic
mouthrinse. Other growth drivers were sales from the acquisition of Vania
Expansion SNC.
Worldwide
Pharmaceutical sales of $5.3 billion for the third quarter represented
a decrease of 14.1% versus the prior year with an operational decline of
11.9% and a negative impact from currency of 2.2%. Domestic sales decreased
19.2%; international sales decreased 7.1%, which reflected an operational
decrease of 1.9% and a negative currency impact of 5.2%.
REMICADE(R)
(infliximab), a biologic approved for the treatment of a number of immune
mediated inflammatory diseases, demonstrated solid sales performance during
the quarter. Several other pharmaceutical products had strong growth including
PREZISTA(R) (darunavir), a treatment for HIV; VELCADE(R) (bortezomib),
a treatment for multiple myeloma; and RISPERDAL(R) CONSTA(R) (risperidone)
Long-Acting Treatment, an antipsychotic medication. Sales results of TOPAMAX(R)
(topiramate), an antiepileptic and a treatment for migraine, and RISPERDAL(R)
(risperidone), an antipsychotic medication, were negatively impacted by
generic competition. ...
Johnson
& Johnson Reports 2009 Second-Quarter Results:
See
text copy below:
Johnson
& Johnson Reports 2009 Second-Quarter Results:
--Sales
of $15.2 Billion Decreased 7.4% Versus 2008 Second Quarter --EPS of $1.15
Decreased 2.5%* Versus 2008 Second Quarter, Excluding 2008 Special Items
NEW
BRUNSWICK, N.J., July 14, 2009 /PRNewswire-FirstCall via COMTEX News Network/
-- Johnson & Johnson (NYSE: JNJ) today announced sales of $15.2
billion for the second quarter of 2009, a decrease of 7.4% as compared
to the second quarter of 2008. Operational results declined 1.4% and the
negative impact of currency was 6.0%. Domestic sales declined 6.7%,
while international sales declined 8.0%, reflecting operational growth
of 3.9% and a negative currency impact of 11.9%.
Net
earnings and diluted earnings per share for the second quarter of 2009
were $3.2 billion and $1.15, respectively. The second quarter of 2008 included
an after-tax in-process research and development charge of $40 million.
Excluding this charge, net earnings for the quarter and diluted earnings
per share represent decreases of 4.7% and 2.5%, respectively, as compared
to the same period in 2008.* The Company confirmed its earnings guidance
for full-year 2009 of $4.45 - $4.55 per share, which excludes the
impact of special items.
"I
am proud of the accomplishments of our people in continuing to deliver
very solid operational results in light of the significant impacts of patent
expirations and the economic environment," said William C. Weldon, Chairman
and Chief Executive Officer. "Our investments through internal research
and development, strategic partnerships and acquisitions have allowed us
to build what is considered by many to be one of the best pipelines in
our industry. We will continue to invest in our portfolio of innovative
products to meet the needs of patients and consumers around the world."
Worldwide
Consumer sales of $3.9 billion for the second quarter represented a decrease
of 4.5% versus the prior year with an increase of 3.1% operationally and
a negative impact from currency of 7.6%. Domestic sales increased 0.8%;
while international sales decreased 8.4%, which reflected an operational
increase of 4.7% and a negative currency impact of 13.1%.
LISTERINE(R)
antiseptic mouthrinse and the skin care lines of NEUTROGENA(R) and AVEENO(R)
contributed to operational sales growth during the quarter. Other growth
drivers were sales from the recently completed acquisition of the French
company Vania Expansion SNC.
Worldwide
Pharmaceutical sales of $5.5 billion for the second quarter represented
a decrease versus the prior year of 13.3% with an operational decline of
8.5% and a negative impact from currency of 4.8%. Domestic sales decreased
16.4%; while international sales decreased 8.7%, which reflected an operational
increase of 3.3% and a negative currency impact of 12.0%.
REMICADE(R)
(infliximab), a biologic approved for the treatment of a number of immune
mediated inflammatory diseases; PREZISTA(R) (darunavir), a treatment for
HIV; VELCADE(R) (bortezomib), a treatment for multiple myeloma; and CONCERTA(R)
(methylphenidate HCI), a treatment for attention deficit hyperactivity
disorder, had strong operational sales performance during the quarter.
Sales results of TOPAMAX(R) (topiramate), an anti-epileptic, and RISPERDAL(R)
(risperidone), an antipsychotic medication, were negatively impacted by
generic competition.
During
the quarter, the U.S. Food and Drug Administration (FDA) approved SIMPONI(TM)
(golimumab) for the treatment of adults with moderately to severely active
rheumatoid arthritis in combination with methotrexate, active psoriatic
arthritis with or without methotrexate, and active ankylosing spondylitis.
The FDA also approved the Supplemental New Drug Applications (sNDAs) for
the use of RISPERDAL(R) CONSTA(R) (risperidone) Long-Acting Treatment as
both monotherapy and adjunctive therapy to lithium or valproate in the
maintenance treatment of Bipolar I Disorder. The Drug Enforcement Administration
(DEA) issued their final ruling and placed NUCYNTA(TM) (tapentadol) CII
immediate release tablets for the relief of moderate to severe acute pain
in patients 18 years of age or older into Schedule II of the Controlled
Substances Act. The product is now available to patients.
The
Company also announced a definitive agreement to acquire Cougar Biotechnology,
a development stage biopharmaceutical company with a specific focus on
oncology, for approximately $1.0 billion in a cash tender offer.
On July 9, 2009, the acquisition of Cougar Biotechnology was completed.
On July 2, 2009, the Company announced a definitive agreement with Elan
Corporation, plc. whereby Johnson & Johnson will acquire substantially
all of the assets and rights of Elan related to its Alzheimer's Immunotherapy
Program and will invest $1 billion in Elan newly issued American Depositary
Receipts (ADRs).
Worldwide
Medical Devices and Diagnostics sales of $5.9 billion for the second quarter
represented a decrease of 3.1% versus the prior year with an operational
increase of 2.9% and a negative currency impact of 6.0%. Domestic sales
increased 1.9%; while international sales decreased 7.2%, which reflected
an operational increase of 3.7% and a negative currency impact of 10.9%.
Primary
contributors to the operational growth included Ethicon's surgical care
products; Ortho-Clinical Diagnostics' professional products; Ethicon Endo-Surgery's
minimally invasive products; and DePuy's orthopaedic joint reconstruction,
spine, and sports medicine businesses. Also contributing to growth were
sales of products acquired as part of the completed acquisition of Mentor
Corporation, a leading supplier of medical products for the global aesthetic
market. This growth was partially offset by lower sales in the Cordis franchise,
reflecting new competitive entries in the drug-eluting stent market as
well as the 2008 divestiture of the Professional Wound Care products in
our Ethicon business.
Johnson
& Johnson has added a new press release to the Investor Relations section
of the Company's Web site
NEW
BRUNSWICK, N.J., July 10, 2009 /PRNewswire-FirstCall via COMTEX News Network/
-- Johnson & Johnson (NYSE: JNJ) today announced it has successfully
completed its acquisition of Cougar Biotechnology, Inc., a development
stage biopharmaceutical company with a specific focus on oncology.
Johnson
& Johnson's tender offer for shares of Cougar Biotechnology common
stock expired at 5 p.m. Eastern Daylight Time (EDT) yesterday with approximately
20,148,930 shares tendered, representing approximately 95.9% of Cougar
Biotechnology's outstanding common stock. The acquisition was completed
yesterday through what is known as a "short-form" merger, without a vote
or meeting of Cougar Biotechnology's remaining shareholders.
Cougar
Biotechnology currently is conducting two Phase III trials for abiraterone
acetate, a late stage, first-in-class compound for the treatment of prostate
cancer. The first Phase III trial is testing abiraterone acetate in patients
with metastatic, castration-resistant prostate cancer who have progressed
after docetaxel-based chemotherapy has failed. The second Phase III trial
is studying abiraterone acetate in patients with metastatic, castration-resistant
prostate cancer who have yet to receive chemotherapy.
One
in six men will be diagnosed with prostate cancer in his lifetime, and
the disease accounts for 10 percent of cancer-related deaths in the United
States.
Cougar
Biotechnology now operates as a wholly-owned subsidiary of Johnson &
Johnson and will work with Ortho Biotech Oncology Research & Development,
a unit of Centocor Research & Development, Inc., a Johnson & Johnson
company.
"With
the acquisition of Cougar Biotechnology and its talented team, we have
strengthened our position in the global oncology market and our efforts
to provide a meaningful difference in the lives of millions of patients
worldwide," said William N. Hait, M.D., Ph.D., Global Therapeutic Head,
Oncology, Ortho Biotech Oncology Research & Development. "Abiraterone
acetate now becomes one of many new treatments we are developing, which
we hope will change the course of cancer treatment by targeting cancer
cells and the tumor microenvironment."
About
Johnson & Johnson
Caring
for the world, one person at a time ... inspires and unites the people
of Johnson & Johnson. We embrace research and science -- bringing innovative
ideas, products and services to advance the health and well-being of people.
Our 119,000 employees at more than 250 Johnson & Johnson companies
work with partners in health care to touch the lives of over a billion
people every day, throughout the world |