�Bayer HealthCare Pharmaceuticals, Inc. and Onyx Pharmaceuticals, Inc.
(Nasdaq: ONXX) announced the companies take in begun enrolling patients
in the STORM Sorafenib as Adjuvant Treatment in the Prevention of
Recurrence of Hepatocellular Carcinoma trial. The randomized, double blind,
placebo-controlled Phase 3 study is evaluating Nexavar(R) (sorafenib)
tablets as adjuvant handling, which is treatment following surgery or
local radiation, for patients with hepatocellular carcinoma (HCC), or
primary liver cancer.
"Nexavar is the only systemic therapy with proven efficacy and
tolerability in HCC across multiple patient populations," aforesaid Dimitris
Voliotis, MD, vice president, Nexavar Clinical Development, Bayer
HealthCare Pharmaceuticals. "Liver cancer is the third largest world
cancer killer worldwide and there is a important need for new therapies
that can buoy be used at all stages in the course of action of the disease to delay
disease progression and prolong life."
In addition, the U.S. Food and Drug Administration (FDA) has completed
a Special Protocol Assessment (SPA) for the STORM test. An SPA is a
written arrangement on the design and size of a clinical trial intended to
form the basis for a new drug application.
Phase 3 Trial Design
The international multicenter study is expected to inscribe approximately
1,100 patients and volition include patients who have received surgical
resection or local excision. The survey will see at whether providing oral
Nexavar in the adjuvant setting delays the prison term to return and increases
overall survival. The primary endpoint of the study is return free
endurance. Secondary endpoints include boilersuit survival, time to recurrence,
patient-reported outcomes, plasma biomarkers, safety and tolerability.
The study is enrolling patients with all HCC histologies. Patients will
be randomized to incur 400 mg of Nexavar twice casual or coordinated placebo
for up to four geezerhood. The discipline will be conducted at more than 200 sites in
North America, South America, Europe and the Asia-Pacific region, including
Japan. For information about enrolling in the study, please visit
hypertext transfer protocol://www.clinicaltrials.gov.
Hepatocellular carcinoma is the most common shape of liver cancer and is
responsible for about 90 pct of the primary malignant liver tumors in
adults. Liver cancer is the sixth most common cancer in the world and the
third base leading cause of cancer-related deaths globally. More than 600,000
cases of liver cancer are diagnosed worldwide each year (more than cd,000
in China, South Korea, Japan and Taiwan, 54,000 in the European Union, and
15,000 in the United States) and the relative incidence is increasing. In 2002,
approximately 600,000 people died of liver cancer the Crab including some
370,000 in China, South Korea and Japan, 57,000 in the European Union, and
13,000 in the United States.(1,2)
Currently there are no adjuvant treatments with proven benefit in HCC
and half of the patients wHO have undergone surgical resection or local
ablation will see their tumors render within 3 years and 70 percent
will witness their tumors return within five years.(3)
Nexavar's Differentiated Mechanism
Nexavar targets both the tumor electric cell and tumor vasculature. In
preclinical studies, Nexavar has been shown to objective members of two
classes of kinases known to be involved in both cell proliferation (growth)
and angiogenesis (origin supply) -- two important processes that enable
crab growth. These kinases included Raf kinase, VEGFR-1, VEGFR-2,
VEGFR-3, PDGFR-B, KIT, FLT-3 and RET.
Nexavar is currently sanctioned in more than 40 countries for liver
genus Cancer and in more than 70 countries for the treatment of patients with
advanced kidney cancer. Nexavar is likewise being evaluated by the companies,
outside study groups, government agencies and single
investigators as a single agent or combination treatment in a wide range of
cancers, including metastatic melanoma, lung cancer, white meat cancer and as
an adjuvant therapy for kidney cancer.
Important Safety Considerations For Patients Taking Nexavar
Based on the currently sanctioned U.S. software insert for the treatment
of patients with unresectable hepatocellular carcinoma, hypertension english hawthorn
occur early in the course of therapy and blood pressure should be monitored
weekly during the first six-spot weeks of therapy and treated as needed.
Bleeding with a fatal consequence from any site was reported in 2.4% for
Nexavar and 4% in placebo. The incidence of treatment-emergent cardiac
ischemia/infarction was 2.7% for Nexavar vs. 1.3% for placebo. Most plebeian
adverse events reported with Nexavar in patients with unresectable HCC were
looseness of the bowels, fatigue, ab pain, weight loss, anorexia, nausea and
hand-foot skin reaction. Grade 3/4 inauspicious events were 45% for Nexavar vs.
32% for placebo. Women of accouchement potential should be advised to
quash becoming meaning and advised against nursing. In cases of whatever
severe or persistent position effects, temporary treatment disruption, dose
qualifying or lasting discontinuation should be considered.
About Bayer HealthCare Pharmaceuticals Inc.
Bayer HealthCare Pharmaceuticals Inc. is the U.S.-based pharmaceuticals
unit of Bayer HealthCare LLC, a division of Bayer AG. One of the world's
leading, modern companies in the healthcare and medical products
manufacture, Bayer HealthCare combines the global activities of the Animal
Health, Consumer Care, Diabetes Care, and Pharmaceuticals divisions. In the
U.S., Bayer HealthCare Pharmaceuticals comprises the following business
units: Women's Healthcare, Diagnostic Imaging, Specialized Therapeutics,
Hematology/Cardiology and Oncology. The company's get is to discover and
manufacture products that will improve human health global by
diagnosis, preventing and treating diseases.
About Onyx Pharmaceuticals, Inc.
Onyx Pharmaceuticals, Inc. is a biopharmaceutical company committed to
improving the lives of people with cancer. The company, in collaboration
with Bayer HealthCare Pharmaceuticals, Inc., is developing and marketing
Nexavar(R) (sorafenib) tablets, a small particle drug. For more info
about Onyx, visit the company's internet site at http://www.onyx-pharm.com.
Forward Looking Statements
This news release may contain forward-looking statements based on
current assumptions and forecasts made by Bayer Group or subgroup
management. Various known and unknown risks, uncertainties and other
factors could lead to material differences between the actual future
results, financial situation, development or performance of the company and
the estimates given here. These factors include those discussed in Bayer's
populace reports which are uncommitted on the Bayer Web site at
http://www.bayer.com. The party assumes no liability whatsoever to update
these modern statements or to conform them to future events or
developments.
This news show release as well contains "innovative statements" of Onyx
inside the substance of the federal securities laws. These forward-looking
statements include without limitation, statements regarding the results of
the clinical development, refuge, regulatory processes, commercialization
efforts or commercial potential of Nexavar. These statements are subject to
risks and uncertainties that could cause actual results and events to
differ materially from those anticipated. Reference should be made to
Onyx's Annual Report on Form 10-K for the year ended % 31, 2007,
filed with the Securities and Exchange Commission under the heading "Risk
Factors" and Onyx's Quarterly Reports on Form 10-Q for a more elaborated
description of such factors. Readers ar cautioned not to place undue
trust on these forward-looking statements that talk only as of the date
of this release. Onyx undertakes no responsibility to update publicly whatever
forward-looking statements to reverberate new data, events, or
circumstances after the date of this release except as required by law.
Nexavar(R) (sorafenib) tablets is a registered trademark of Bayer
HealthCare Pharmaceuticals, Inc.
References
(1) Ferlay J, et al., GLOBOCAN 2002. Cancer Incidence, Mortality and
Prevalence Worldwide. IARC CancerBase No.5, Version 2.0. IARCPress,
Lyon, 2004. Available at: hTTP://www-dep.iarc.fr. Accessed May 2008.
(2) 2005 Cancer Register System (CRS) annual report,
http://crs.cph.ntu.edu.tw/crs_c/annual.html. Accessed May 12, 2008.
(3) Del Pozo AC, Lopez P. Management of hepatocellular carcinoma. Clin
Liver Dis 2007 May;11(2):305-21.
Onyx Pharmaceuticals, Inc
http://www.onyx-pharm.com
View dose information on Nexavar.
More information
Saturday 23 August 2008
Wednesday 13 August 2008
Download Twista
 Artist: Twista: mp3 download Genre(s): Rap: Hip-Hop Other Discography:  Adrenaline Rush 2007 Year: 2007 Tracks: 19  Twista Year: 2004 Tracks: 1  The Day After Year: 2004 Tracks: 15  Kamikaze Year: 2004 Tracks: 16 Chicago rapper Twista made his transcription debut on "Po Pimp," a atomic number 78 single by his dude Windy City rappers Do or Die. Following "Po Pimp," Twista sign-language with Big Beat/Atlantic and released his debut, Adrenalin Rush, in the summer of 1997. Mobstability followed a year later, and in 1999 Twista returned with Legit Ballin'. In settle 2002, Twista hooked up with Ludacris, Jay-Z, Bone Thugs-N-Harmony and other tap moguls for the transcription of his third record album. Kamikaze came out at the beginning of 2004 and readily stumble the Billboard cc, horseback horseback riding the impulsion of his #1 stumble single "Dull Jamz." In 2005 he returned with the record album The Day After and the run into single "Girl Tonite" with Trey Songz. Two eld by and by Adrenaline Rush 2007 appeared. |
Melba Moore
Wednesday 6 August 2008
New York Times Examines Reaction To Tobacco Regulation Legislation
�
The New York Times on Sunday examined how smokers ar left in the middle of "this maelstrom of debate" on whether menthol-flavored cigarettes should be included in the legislation that would allow FDA to ban flavored additives (Navarro, New York Times, 8/3).
The House last week by a veto-proof 326-102 vote approved lawmaking (HR 1108) that would give FDA the confidence to determine tobacco products. The metre, introduced by Rep. Henry Waxman (D-Calif.), would allow FDA to ban flavored additives, with an exemption for menthol flavoring. Some black anti-smoking advocates criticized the exemption, noting that many black smokers use mentholated cigarettes. The National African American Tobacco Prevention Network withdrew its support for the bill because of the menthol exemption. Seventy-five pct of black smokers economic consumption mentholated tobacco products. Menthol brands account for about 28% of the $70 billion U.S. cigarette market.
It is intellection that menthol and other additives mightiness mask the harshness of tobacco, which could cook it easier for teenagers to begin smoking. Researchers also receive questioned whether menthol plays a character in disproportional rates of cancer related to to smoking among blacks. A recent study from Harvard University found that some butt makers by choice "manipulated menthol levels to attract young people" (Kaiser Health Disparities Report, 7/31).
The Times reports that menthol cigarettes have historically been heavily marketed in black communities and that blacks have disproportionately higher rates of death and disease related to smoking, according to the Times. According to the Times, some smokers "refuse such wholesale interference with personal choices" and others "believe that having their menthol cigarettes snatched away may be just what they motive to oddment their habit."
The Times notes that it "may take more than a ban -- or the health warnings or the $5 pack -- to stop some smokers." Justine Love -- a 54-year-old black Washington, D.C., wireless personality wHO smoked menthol cigarettes for 30 geezerhood and now gives testimonials and public service announcements on her radio station -- said, "This is a very personal decision, and you don't need anybody to tell you what you can or can't do." She adds, "I don't say, 'You should halt smoking.' I give encouragement to quit. I tell them I saved $139 in the get-go month" (New York Times, 8/3).
Reprinted with kind permission from http://www.kaisernetwork.org. You can view the entire Kaiser Daily Health Policy Report, search the archives, or sign up for electronic mail delivery at http://www.kaisernetwork.
The New York Times on Sunday examined how smokers ar left in the middle of "this maelstrom of debate" on whether menthol-flavored cigarettes should be included in the legislation that would allow FDA to ban flavored additives (Navarro, New York Times, 8/3).
The House last week by a veto-proof 326-102 vote approved lawmaking (HR 1108) that would give FDA the confidence to determine tobacco products. The metre, introduced by Rep. Henry Waxman (D-Calif.), would allow FDA to ban flavored additives, with an exemption for menthol flavoring. Some black anti-smoking advocates criticized the exemption, noting that many black smokers use mentholated cigarettes. The National African American Tobacco Prevention Network withdrew its support for the bill because of the menthol exemption. Seventy-five pct of black smokers economic consumption mentholated tobacco products. Menthol brands account for about 28% of the $70 billion U.S. cigarette market.
It is intellection that menthol and other additives mightiness mask the harshness of tobacco, which could cook it easier for teenagers to begin smoking. Researchers also receive questioned whether menthol plays a character in disproportional rates of cancer related to to smoking among blacks. A recent study from Harvard University found that some butt makers by choice "manipulated menthol levels to attract young people" (Kaiser Health Disparities Report, 7/31).
The Times reports that menthol cigarettes have historically been heavily marketed in black communities and that blacks have disproportionately higher rates of death and disease related to smoking, according to the Times. According to the Times, some smokers "refuse such wholesale interference with personal choices" and others "believe that having their menthol cigarettes snatched away may be just what they motive to oddment their habit."
The Times notes that it "may take more than a ban -- or the health warnings or the $5 pack -- to stop some smokers." Justine Love -- a 54-year-old black Washington, D.C., wireless personality wHO smoked menthol cigarettes for 30 geezerhood and now gives testimonials and public service announcements on her radio station -- said, "This is a very personal decision, and you don't need anybody to tell you what you can or can't do." She adds, "I don't say, 'You should halt smoking.' I give encouragement to quit. I tell them I saved $139 in the get-go month" (New York Times, 8/3).
Reprinted with kind permission from http://www.kaisernetwork.org. You can view the entire Kaiser Daily Health Policy Report, search the archives, or sign up for electronic mail delivery at http://www.kaisernetwork.
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