THOUSAND OAKS, Calif. and COLLEGEVILLE, Pa., Oct 24, 2003 -- Data on Enbrel(R) (etanercept) demonstrate improvements that were sustained
for more than one year in many patients in both the joint symptoms and skin
lesions associated with psoriatic arthritis, according to reports presented
this week at the American College of Rheumatology´s (ACR) Annual Scientific
Meeting in Orlando, Fla. Additional ENBREL data showed that patients with
ankylosing spondylitis (AS) experienced statistically significant improvements
in patient-reported outcomes, including pain, fatigue and functional status.
Psoriatic arthritis and AS belong to a group of diseases referred to as
the spondylarthropathies. Spondylarthropathies are arthritic in nature, can
affect the spine and joints and can occur in young adults, commonly beginning
before the age of 35. ENBREL is the only therapy approved to reduce signs and
symptoms and inhibit the progression of structural damage of active arthritis
in patients with psoriatic arthritis and is the only anti-TNF receptor
approved to reduce signs and symptoms in patients with active AS.
Sustained Efficacy, Tolerability and Improved Function in Psoriatic
In an open-label extension study of 169 patients, ENBREL was generally
well-tolerated and demonstrated sustained efficacy, reducing clinical signs
and symptoms of psoriatic arthritis for up to 106 weeks in many patients.
These patients experienced less joint pain, fewer swollen joints and exhibited
At 48 weeks (n=145), 66 percent of patients treated with ENBREL achieved
an ACR 20, and 47 percent achieved an ACR 50 (improvement in ACR score of
20 or 50 percent, respectively). Fifty-seven percent of patients also had
substantial clearing of their psoriasis plaques.
Patients also completed a Health Assessment Questionnaire (HAQ), which
included measures of vitality and questions regarding activities of daily
living. Thirty-nine percent of patients achieved a HAQ score of zero,
indicating no functional disability, at 48 weeks. In another analysis of
these psoriatic arthritis patients (n=69), many of those treated with ENBREL
experienced a significant, rapid and sustained increase in their ability to
perform daily activities such as walking, dressing, grooming and gripping, for
up to 72 weeks as assessed by HAQ scores.
"Patients with psoriatic arthritis experience painful and debilitating
symptoms that affect many basic activities, such as dressing, that most of us
take for granted," said Philip Mease, M.D., lead study investigator and chief
of rheumatology clinical research at Swedish Hospital Medical Center in
Seattle. "It is gratifying as a physician to see patients on ENBREL
experiencing long-term improvement of painful joints and unsightly skin
lesions, allowing them to resume normal activities of daily living and
participate confidently in family, social and work life."
Ankylosing Spondylitis Patients Feel Improvements With ENBREL Treatment
In a landmark Phase 3 study, patients taking ENBREL experienced rapid and
statistically significant improvements in patient-reported outcomes, including
pain, overall disease activity, function and fatigue in as early as two weeks,
compared with patients receiving placebo.
After six months, 57 percent of patients achieved a 20 percent improvement
in the Assessment on Ankylosing Spondylitis Response Criteria (ASAS 20)
compared to 22 percent for those taking placebo. ASAS is a composite measure
that includes back pain, morning stiffness, inflammation and physical
function. Approximately 17 percent of patients achieved partial remission,
compared to four percent taking placebo. Partial remission, as defined by
ASAS is a low disease activity level (absolute score less than or equal to
20 for the four ASAS criteria).
"ENBREL actually induced partial remission in some patients in a very
short time after initiation of treatment," said John C. Davis, M.D.,
University of California, San Francisco. "This was a significant improvement
for these patients."
About Psoriatic Arthritis
Psoriatic arthritis is a chronic inflammatory disease of the joints and
connective tissue. The disease involves joint pain and swelling that can lead
to debilitation with inflamed and irritated scaly red patches of skin. The
disease can be difficult to diagnose, particularly in its milder forms and
earlier stages. Up to one million people in the U.S. population have
psoriatic arthritis. ENBREL is the first and only biologic approved to reduce
the signs and symptoms and to inhibit the progression of structural damage of
active arthritis in patients with psoriatic arthritis.
Ankylosing spondylitis, which affects approximately 350,000 people in the
United States, is a painful, and potentially progressive inflammatory disease
affecting joints and ligaments that normally allow a person´s back to move and
flex. The spine can fuse, causing loss of motion and a permanent stooped-over
posture. AS frequently strikes between the ages of 16 and 30 and tends to
affect more men than women.
ENBREL is the only fully human TNF receptor approved to reduce signs and
symptoms, improve physical function, and inhibit the progression of structural
damage in patients with moderately to severely active rheumatoid arthritis
(RA), and to reduce the signs and symptoms and inhibit the progression of
structural damage of active arthritis in patients with psoriatic arthritis.
ENBREL is the only biologic therapy approved for first-line treatment of RA
patients, and can be used alone or in combination with methotrexate. It is
approved to reduce the signs and symptoms of moderately to severely active
polyarticular-course juvenile rheumatoid arthritis (JRA) in patients who have
had an inadequate response to one or more disease-modifying antirheumatic
drugs (DMARDs). It is also the first biologic approved to treat the signs and
symptoms in patients with active ankylosing spondylitis (AS).
ENBREL has been used by more than 200,000 patients worldwide across
indications since becoming commercially available nearly five years ago.
ENBREL acts by binding TNF, one of the dominant inflammatory cytokines or
regulatory proteins that play an important role in both normal immune function
and the cascade of reactions that causes the inflammatory process of RA, JRA,
psoriatic arthritis and AS. The binding of ENBREL to TNF renders the bound
TNF biologically inactive, resulting in significant reduction in inflammatory
Adverse events in psoriatic arthritis and AS clinical trials were similar
to those reported in previous clinical trials of ENBREL in patients with
rheumatoid arthritis. There was no increase in the number of serious adverse
events occurring in patients treated with ENBREL compared to those receiving
placebo. Only the rate of injection site reactions (ISRs) in patients
receiving ENBREL was statistically different compared to those receiving
placebo (36 percent with ENBREL versus 9 percent in placebo-treated patients).
Since the product was first introduced, the following have been reported
in patients using ENBREL:
* Serious Infections
- Many occurred in people prone to infection, such as those with
advanced or poorly controlled diabetes
- Some serious infections were fatal
- Rare cases of tuberculosis
* What to do / Not do
- Do not start ENBREL if you have an infection or are allergic to
ENBREL or its components
- Tell your doctor if you are prone to infection
- Stop ENBREL if a serious infection occurs
- Contact your doctor if you have questions about ENBREL or develop
* Serious nervous system disorders such as multiple sclerosis, seizures,
or inflammation of the nerves of the eyes.
- Tell your doctor if you have ever had any of these disorders or if
you develop them after starting ENBREL
* Rare reports of serious blood disorders (some fatal)
- Contact your doctor immediately if you develop symptoms such as
persistent fever, bruising, bleeding, or paleness
* In medical studies of all TNF-inhibitors, a higher rate of lymphoma (a
type of cancer) was seen compared to the general population, however,
the risk of lymphoma may be up to several fold higher in RA patients.
The role of TNF-inhibitors in the development of lymphoma is unknown.
* The incidence of other cancers has not increased with extended
exposure to ENBREL and is similar to the expected rate.
* ENBREL can also cause injection site reactions.
* In a medical study of patients with JRA, infections, headaches,
abdominal pain, vomiting, and nausea occurred more frequently than in
- The kinds of infections reported were generally mild and similar to
those usually seen in children
- Other serious adverse reactions were reported rarely, including
serious infections (two percent) and depression/personality
disorder (one percent)
Amgen and Wyeth Pharmaceuticals, a division of Wyeth, market ENBREL in
North America. Wyeth markets ENBREL outside of North America. Immunex
Corporation, a wholly owned subsidiary of Amgen, manufactures ENBREL.
Additional information about ENBREL, including full Prescribing Information,
can be found on the Web site sponsored by the companies at www.enbrel.com or
by calling toll free 888-4ENBREL (888-436-2735).
Amgen is a global biotechnology company that discovers, develops,
manufactures and markets important human therapeutics based on advances in
cellular and molecular biology.
Wyeth Pharmaceuticals, a division of Wyeth, has leading products in the
areas of women´s health care, cardiovascular disease, central nervous system,
inflammation, hemophilia, oncology and vaccines. Wyeth is one of the world´s
largest research-driven pharmaceutical and health care products companies. It
is a leader in the discovery, development, manufacturing, and marketing of
pharmaceuticals, vaccines, biotechnology products and non-prescription
medicines that improve the quality of life for people worldwide. The
Company´s major divisions include Wyeth Pharmaceuticals, Wyeth Consumer
Healthcare and Fort Dodge Animal Health.
This news release contains forward-looking statements that involve
significant risks and uncertainties, including those discussed below and
others that can be found in Amgen´s Form 10-K for the year ended December 31,
2002, and in Amgen´s periodic reports on Form 10-Q and Form 8-K. Amgen is
providing this information as of the date of this news release and does not
undertake any obligation to update any forward-looking statements contained in
this document as a result of new information, future events or otherwise.
No forward-looking statement can be guaranteed and actual results may
differ materially from those we project. Amgen´s results may be affected by
its ability to successfully market both new and existing products domestically
and internationally, sales growth of recently launched products, difficulties
or delays in manufacturing its products, and regulatory developments (domestic
or foreign) involving current and future products and manufacturing
In addition, sales of Amgen´s products are affected by reimbursement
policies imposed by third party payors, including governments, private
insurance plans and managed care providers, and may be affected by domestic
and international trends toward managed care and healthcare cost containment
as well as possible U.S. legislation affecting pharmaceutical pricing and
reimbursement. Government regulations and reimbursement policies may affect
the development, usage and pricing of Amgen´s products. Furthermore, Amgen´s
research, testing, pricing, marketing and other operations are subject to
extensive regulation by domestic and foreign government regulatory
authorities. Amgen or others could identify side effects or manufacturing
problems with its products after they are on the market.
In addition, Amgen competes with other companies with respect to some of
its marketed products as well as for the discovery and development of new
products. Discovery or identification of new product candidates cannot be
guaranteed and movement from concept to product is uncertain; consequently,
there can be no guarantee that any particular product candidate will be
successful and become a commercial product.
In addition, while Amgen routinely obtains patents for its products and
technology, the protection offered by its patents and patent applications may
be challenged, invalidated or circumvented by its competitors. Further, some
raw materials, medical devices and component parts for Amgen´s products are
supplied by sole third party suppliers.
The statements in this press release that are not historical facts are
forward-looking statements based on current expectations of future events that
involve risks and uncertainties including, without limitation, risks
associated with the inherent uncertainty of pharmaceutical research, product
development, manufacturing, and commercialization, and economic conditions,
including interest and currency exchange rate fluctuations, the impact of
competitive or generic products, product liability and other types of
lawsuits, the impact of legislative and regulatory compliance and obtaining
approvals, and patents, and other risks and uncertainties, including those
detailed from time to time in Wyeth´s periodic reports, including quarterly
reports on Form 10-Q and the Annual Report on Form 10-K, filed with the
Securities and Exchange Commission. Actual results may vary materially from
the forward-looking statements. Wyeth assumes no obligation to publicly
update any forward-looking statements, whether as a result of new information,
future events or otherwise.
Media, Andrea Rothschild, +1-805-447-6287, or cell,
+1-818-681-8660, or Investors, Cary Rosansky, +1-805-447-1060, both of Amgen;
or Media, Douglas Petkus, +1-484-865-5140, or Investors, Justin Victoria,
+1-973-660-5340, both of Wyeth Pharmaceuticals