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LOL : $ 0.05 -0.33 (-86.84%) Volume: 800
Short Interest (Shares Short) 1,143,700
Short % Increase 56.12 %
Record Date 2009-OctB
http://www.shortsqueeze.com/?symbol=cxm&submit=Short+Quote%99
LOL - unbelievable
Keryx Biopharmaceuticals, Inc. Announces Upcoming Poster Presentation of Zerenex (ferric citrate) for the Treatment of Hyperphos
Date : 10/26/2009 @ 8:30AM
Source : PR Newswire
Stock : (KERX)
http://ih.advfn.com/p.php?pid=nmona&cb=1256569334&article=40052709&symbol=N^KERX
Phase 2 data on Zerenex as a treatment for hyperphosphatemia for dialysis patients requiring high doses of phosphate binders to be presented on Thursday, October 29, 2009 at 10:00am PDT
NEW YORK, Oct. 26 /PRNewswire-FirstCall/ -- Keryx Biopharmaceuticals, Inc. (NASDAQ:KERX) today announced that an abstract related to the clinical data of the 55-patient Phase 2 high-dose study of Zerenex (ferric citrate) has been accepted for presentation during the poster sessions to be held at the upcoming American Society of Nephrology (ASN) Renal Week Meeting and exposition taking place October 27-November 1 in San Diego, California.
Poster Number: PO-361, entitled "Evaluation of Ferric Citrate as a Phosphate Binder in Dialysis Patients Requiring High Doses of Phosphate Binders" will be presented on Thursday, October 29, 2009 at 10:00am PDT during the "Dialysis: Epidemiology, Outcomes, and Clinical Trials: Non-Cardiovascular I" Poster Session, and will be available for viewing from 10:00am-12:00pm PDT.
Top-line data from the study discussed in the poster was previously announced by the Company.
About Keryx Biopharmaceuticals, Inc.
Keryx Biopharmaceuticals is focused on the acquisition, development and commercialization of medically important pharmaceutical products for the treatment of life-threatening diseases, including cancer and renal disease. Keryx is developing KRX-0401 (perifosine), a novel, potentially first-in-class, oral anti-cancer agent that inhibits the phosphoinositide 3-kinase (PI3K)/Akt pathway, a key signaling cascade that has been shown to induce cell growth and cell transformation. KRX-0401 has demonstrated both safety and clinical efficacy in several tumor types, both as a single agent and in combination with novel therapies. KRX-0401 also modulates a number of other key signal transduction pathways, including the JNK and MAPK pathways, which are pathways associated with programmed cell death, cell growth, cell differentiation and cell survival. KRX-0401 is currently in Phase 2 clinical development for multiple tumor types, with a Phase 3 in multiple myeloma, under Special Protocol Assessment (SPA), pending commencement by year-end. Keryx is also developing Zerenex(TM) (ferric citrate), an oral, iron-based compound that has the capacity to bind to phosphate and form non-absorbable complexes. Zerenex has recently completed a Phase 2 clinical program as a treatment for hyperphosphatemia (elevated phosphate levels) in patients with end-stage renal disease, and Keryx is in the process of finalizing the U.S. Phase 3 program for Zerenex in consultation with the FDA. Keryx is headquartered in New York City.
Cautionary Statement
Some of the statements included in this press release, particularly those anticipating future clinical and business prospects for Zerenex (ferric citrate), may be forward-looking statements that involve a number of risks and uncertainties. For those statements, we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. Among the factors that could cause our actual results to differ materially are the following: our ability to successfully complete clinical trials for Zerenex; our ability to meet anticipated development timelines for Zerenex due to recruitment, clinical trial results, manufacturing capabilities or other factors; our ability to replicate in our planned Phase 3 clinical program the efficacy and safety of Zerenex observed in the previous Phase 2 and the Open Label Extension clinical trials, and the effects on IV iron and EPO use observed in these previous clinical trials; and other risk factors identified from time to time in our reports filed with the Securities and Exchange Commission. Any forward-looking statements set forth in this press release speak only as of the date of this press release. We do not intend to update any of these forward-looking statements to reflect events or circumstances that occur after the date hereof. This press release and prior releases are available at http://www.keryx.com/. The information in our website is not incorporated by reference into this press release and is included as an inactive textual reference only.
KERYX CONTACT: Lauren Fischer Director, Investor Relations Keryx Biopharmaceuticals, Inc.
Tel: 212.531.5962 E-mail:
DATASOURCE: Keryx Biopharmaceuticals, Inc.
CONTACT: Lauren Fischer, Director, Investor Relations, Keryx
Biopharmaceuticals, Inc., +1-212-531-5962,
Web Site: http://www.keryx.com/
CEL-SCI Corporation Strengthens Balance Sheet Through Receipt of $10 Million From Warrant Exercises
Date : 10/26/2009 @ 9:55AM
Source : PR Newswire
Stock : (CVM)
http://ih.advfn.com/p.php?pid=nmona&cb=1256569334&article=40054373&symbol=A^CVM
Completion of Cel-Sci's New Facility Signals That Long Awaited Phase III Trial is Imminent
Date : 10/26/2009 @ 7:15AM
Source : Business Wire
Stock : BiomedReports.com (CVM)
http://ih.advfn.com/p.php?pid=nmona&cb=1256569334&article=40050260&symbol=A^CVM
Inside Cel-Sci's New Multikine Production Facility
Written by Vinny Cassano
Monday, 26 October 2009 00:00
http://biomedreports.com/articles/most-popular/14683-inside-cel-scis-new-multikine-production-facility.html
... -
http://www.gomonews.com/in-praise-of-iain-mccready-ceo-neomedia-and-the-success-of-his-mobile-barcode-licensing-agreements/
Bena: I have to admit Iain, during your time at NeoMedia you have been a soldier. You have had a task list and one by one have managed to tick off the biggest deals and turn the company around. I am very impressed and wasn’t sure that it was possible.
Iain: Our IP was the crucial part in this and that is the main driver. We had a checklist of what we wanted to achieve and you are right nearly every box is ticked.
Bena: So are you going to retire? (laughs)
Iain: No, I have worked too hard to let it go. All guns are blazing and I am ready to take the company to greater levels.
ENCO -
10/19/2009 FORM 4 (10% Owner - Koskelo Ilari)
http://www.sec.gov/Archives/edgar/data/856569/000118143109048040/xslF345X03/rrd255317.xml
http://www.finviz.com/quote.ashx?t=enco&ty=c&ta=0&p=d
...OK - _bbb_ on watch for next week.
After this maybe...
I do not think...
CTIC @ 'The 8th Annual BIO Investor Forum'
An International Forum Featuring Late-Stage Private and Emerging Public Companies
October 28-29, 2009
Palace Hotel
San Francisco, CA
http://investorforum.bio.org/opencms/bif/2009/
Presenting Companies
http://investorforum.bio.org/opencms/bif/2009/companyInfo/PresentingCompanies.html
CTIC -- Thurs, 10/29 10:00am Presidio
JGBO / NEOM
SEC Charges New York Broker for Manipulating Stock Prices Through Fake Press Releases and Internet Postings
http://www.sec.gov/news/press/2009/2009-226.htm
FOR IMMEDIATE RELEASE
2009-226
Washington, D.C., Oct. 22, 2009 — The Securities and Exchange Commission today charged a securities broker from Merrick, N.Y., with securities fraud for repeatedly creating and then distributing fake press releases to manipulate the stock prices of multiple publicly traded companies.
The 8th Annual BIO Investor Forum
An International Forum Featuring Late-Stage Private and Emerging Public Companies
October 28-29, 2009
Palace Hotel
San Francisco, CA
http://investorforum.bio.org/opencms/bif/2009/
Presenting Companies
http://investorforum.bio.org/opencms/bif/2009/companyInfo/PresentingCompanies.html
Novavax to Present at 8th Annual BIO Investor Forum 2009
* Press Release
* Source: Novavax, Inc.
* On 10:00 am EDT, Friday October 23, 2009
http://finance.yahoo.com/news/Novavax-to-Present-at-8th-prnews-1429551029.html?x=0&.v=1
ROCKVILLE, Md., Oct. 23 /PRNewswire-FirstCall/ -- Novavax, Inc. (Nasdaq: NVAX - News) a clinical-stage vaccine company, announced today that Fred W. Driscoll, VP and CFO, will be presenting at the 8th Annual BIO Investor Forum 2009 at 11:00 am local time on October 29, 2009 at the Palace Hotel in San Francisco, California. Mr. Driscoll will provide an overview of the company's business strategy and research and development progress. A link to the live presentation can be accessed via the Company website at www.novavax.com under the Investors tab. An archive of the presentation will be available one hour after the event on the Novavax website for 90 days.
About Bio Investor Forum
The Bio Investor Forum, sponsored by the Biotechnology Industry Organization (BIO), is a national investor forum to explore investment trends and opportunities in life sciences, with a focus on public and venture-stage growth companies as well as those poised to join the growth "watch list" in 2010. This forum is attended by public and private equity investors, research analysts, investment bankers and industry executives focused on investment and business development opportunities in the life sciences.
BIO represents more than 1,200 biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other nations. BIO members are involved in the research and development of innovative healthcare, agricultural, industrial and environmental biotechnology technologies. BIO also produces the annual BIO International Convention, the world's largest gathering of the biotechnology industry, along with industry- leading innovator and partnering meetings held around the world.
About Novavax
Novavax, Inc. is a clinical-stage biotechnology company, creating novel vaccines to address a broad range of infectious diseases worldwide, including H1N1, using advanced proprietary virus-like-particle (VLP) technology. The company produces potent VLP -based, recombinant vaccines utilizing new and efficient manufacturing approaches. Novavax is committed to using its VLP technology to create country-specific vaccine solutions. It recently launched a joint venture with Cadila Pharmaceuticals, named CPL Biologicals, to develop and manufacture vaccines, biological therapeutics and diagnostics in India. Additional information is available on Novavax website: http://www.novavax.com
... the answer of your question you will find, if you open the LINK (@ right side)!
President Has Declared an H1N1 National Emergency
Flu Stock Upturn? President Has Declared an H1N1 National Emergency
Written by Staff and Wire Reports
Saturday, 24 October 2009 07:56
http://biomedreports.com/articles/most-popular/14675-obama-declares-swine-flu-a-national-emergency-.html
President Barack Obama has declared the swine flu outbreak a national emergency. The White House on Saturday said Obama signed a proclamation that would allow medical officials to bypass certain federal requirements.
The declaration that Obama signed allows Health and Human Services chief Kathleen Sebelius to bypass federal rules when opening alternative care sites, such as offsite hospital centers at schools or community centers, if needed.
Hospitals could modify patient rules — for example, requiring them to give less information during a hectic time — to quicken access to treatment, with government approval.
The declaration, which the White House announced Saturday, allows HHS in some cases to let hospitals relocate emergency rooms offsite to reduce flu-related burdens and to protect noninfected patients.
Administration officials said the declaration was a pre-emptive move designed to make decisions easier when they need to be made. Officials said this was not in response to any single development on an outbreak that has lasted months and has killed more than 1,000 people in the United States.
It was the second of two steps needed to give Sebelius extraordinary powers during a crisis. On April 26, the administration declared swine flu a public health emergency, allowing the shipment of roughly 12 million doses of flu-fighting medications from a federal stockpile to states in case they eventually needed them. At the time, there were 20 confirmed cases in the U.S. of people recovering easily. There was no vaccine against swine flu, but the CDC had taken the initial step necessary for producing one.
"As a nation, we have prepared at all levels of government, and as individuals and communities, taking unprecedented steps to counter the emerging pandemic," Obama wrote in the declaration.
Because of vaccine production delays, the government has backed off initial, optimistic estimates that as many as 120 million doses would be available by mid-October. As of Wednesday, only 11 million doses had been shipped to health departments, doctor's offices and other providers, according to the Centers for Disease Control and Prevention officials said.
The government now hopes to have about 50 million doses of swine flu vaccine out by mid-November and 150 million in December.
The flu virus has to be grown in chicken eggs, and the yield hasn't been as high as was initially hoped, officials explained.
In Massachusetts, the Boston Globe is reporting that for the first time this fall, public health authorities described the state’s influenza outbreak as widespread, the highest category on the scale of disease spread. In a weekly surveillance report, officials said they had seen a “dramatic increase in influenza-like illnesses over the past few weeks’’ compared with early fall levels in previous years.
“We had always been predicting this,’’ Dr. Lauren Smith, medical director of the state Department of Public Health, said yesterday. “We knew the H1N1 [swine flu] virus was going to be increasing. We didn’t know when, but now we do. It’s here.’’
It was just six months ago that the U.S. Centers for Disease Control and Prevention reported that two children in California had developed a respiratory illness never before seen in humans, referring to the infection as "swine flu" in its Morbidity and Mortality Weekly Report.
Flu activity is now widespread in 46 states. Nationwide, visits to doctors for influenza-like-illness are increasing steeply and are now higher than what is seen at the peak of many regular flu seasons. In addition, flu-related hospitalizations and deaths continue to go up nation-wide and are above what is expected for this time of year.
Below is a summary of the most recent key indicators:
Visits to doctors for influenza-like illness (ILI) increased steeply since last week in the United States, and overall, are much higher than what is expected for this time of the year. ILI activity now is higher than what is seen during the peak of many regular flu seasons.
Total influenza hospitalization rates for laboratory-confirmed flu are climbing and are higher than expected for this time of year.
The proportion of deaths attributed to pneumonia and influenza (P&I) based on the 122 Cities Report has increased and has been higher than what is expected at this time of year for two weeks. In addition, 11 flu-related pediatric deaths were reported this week; 9 of these deaths were confirmed 2009 H1N1, and two were influenza A viruses, but were not subtyped. Since April 2009, CDC has received reports of 95 laboratory-confirmed pediatric 2009 H1N1 deaths and another 7 pediatric deaths that were laboratory confirmed as influenza, but where the flu virus subtype was not determined.
Forty-six states are reporting widespread influenza activity at this time. They are: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, and Wyoming. This many reports of widespread activity are unprecedented during seasonal flu.
Almost all of the influenza viruses identified so far are 2009 H1N1 influenza A viruses. These viruses remain similar to the virus chosen for the 2009 H1N1 vaccine, and remain susceptible to the antiviral drugs oseltamivir and zanamivir with rare exception.
Last week the CDC reported that influenza activity increased dramatically in the U.S.
4,855 (37.5%) specimens tested by U.S. World Health Organization (WHO) and National Respiratory and Enteric Virus Surveillance System (NREVSS) collaborating laboratories and reported to CDC/Influenza Division were positive for influenza.
All subtyped influenza A viruses being reported to CDC were 2009 influenza A (H1N1) viruses.
The proportion of deaths attributed to pneumonia and influenza (P&I) was above the epidemic threshold.
Eleven influenza-associated pediatric deaths were reported. Nine of these deaths were associated with 2009 influenza A (H1N1) virus infection and two were associated with an influenza A virus for which subtype is undetermined.
The proportion of outpatient visits for influenza-like illness (ILI) was above the national baseline. All 10 regions reported ILI above region-specific baseline levels.
Forty-six states reported geographically widespread influenza activity, Guam and three states reported regional influenza activity, one state, the District of Columbia, and Puerto Rico reported local influenza activity, and the U.S. Virgin Islands did not report.
Companies with Potential Vaccines
and Treatments for Swine Flu
Novavax, Inc. (NASDAQ:NVAX)
Product: Swine Flu Vaccines
using Virus-like particle (VLP) technology
Flu Stock Upturn? President Has Declared an H1N1 National Emergency
Written by Staff and Wire Reports
Saturday, 24 October 2009 07:56
http://biomedreports.com/articles/most-popular/14675-obama-declares-swine-flu-a-national-emergency-.html
President Barack Obama has declared the swine flu outbreak a national emergency. The White House on Saturday said Obama signed a proclamation that would allow medical officials to bypass certain federal requirements.
The declaration that Obama signed allows Health and Human Services chief Kathleen Sebelius to bypass federal rules when opening alternative care sites, such as offsite hospital centers at schools or community centers, if needed.
Hospitals could modify patient rules — for example, requiring them to give less information during a hectic time — to quicken access to treatment, with government approval.
The declaration, which the White House announced Saturday, allows HHS in some cases to let hospitals relocate emergency rooms offsite to reduce flu-related burdens and to protect noninfected patients.
Administration officials said the declaration was a pre-emptive move designed to make decisions easier when they need to be made. Officials said this was not in response to any single development on an outbreak that has lasted months and has killed more than 1,000 people in the United States.
It was the second of two steps needed to give Sebelius extraordinary powers during a crisis. On April 26, the administration declared swine flu a public health emergency, allowing the shipment of roughly 12 million doses of flu-fighting medications from a federal stockpile to states in case they eventually needed them. At the time, there were 20 confirmed cases in the U.S. of people recovering easily. There was no vaccine against swine flu, but the CDC had taken the initial step necessary for producing one.
"As a nation, we have prepared at all levels of government, and as individuals and communities, taking unprecedented steps to counter the emerging pandemic," Obama wrote in the declaration.
Because of vaccine production delays, the government has backed off initial, optimistic estimates that as many as 120 million doses would be available by mid-October. As of Wednesday, only 11 million doses had been shipped to health departments, doctor's offices and other providers, according to the Centers for Disease Control and Prevention officials said.
The government now hopes to have about 50 million doses of swine flu vaccine out by mid-November and 150 million in December.
The flu virus has to be grown in chicken eggs, and the yield hasn't been as high as was initially hoped, officials explained.
In Massachusetts, the Boston Globe is reporting that for the first time this fall, public health authorities described the state’s influenza outbreak as widespread, the highest category on the scale of disease spread. In a weekly surveillance report, officials said they had seen a “dramatic increase in influenza-like illnesses over the past few weeks’’ compared with early fall levels in previous years.
“We had always been predicting this,’’ Dr. Lauren Smith, medical director of the state Department of Public Health, said yesterday. “We knew the H1N1 [swine flu] virus was going to be increasing. We didn’t know when, but now we do. It’s here.’’
It was just six months ago that the U.S. Centers for Disease Control and Prevention reported that two children in California had developed a respiratory illness never before seen in humans, referring to the infection as "swine flu" in its Morbidity and Mortality Weekly Report.
Flu activity is now widespread in 46 states. Nationwide, visits to doctors for influenza-like-illness are increasing steeply and are now higher than what is seen at the peak of many regular flu seasons. In addition, flu-related hospitalizations and deaths continue to go up nation-wide and are above what is expected for this time of year.
Below is a summary of the most recent key indicators:
Visits to doctors for influenza-like illness (ILI) increased steeply since last week in the United States, and overall, are much higher than what is expected for this time of the year. ILI activity now is higher than what is seen during the peak of many regular flu seasons.
Total influenza hospitalization rates for laboratory-confirmed flu are climbing and are higher than expected for this time of year.
The proportion of deaths attributed to pneumonia and influenza (P&I) based on the 122 Cities Report has increased and has been higher than what is expected at this time of year for two weeks. In addition, 11 flu-related pediatric deaths were reported this week; 9 of these deaths were confirmed 2009 H1N1, and two were influenza A viruses, but were not subtyped. Since April 2009, CDC has received reports of 95 laboratory-confirmed pediatric 2009 H1N1 deaths and another 7 pediatric deaths that were laboratory confirmed as influenza, but where the flu virus subtype was not determined.
Forty-six states are reporting widespread influenza activity at this time. They are: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, and Wyoming. This many reports of widespread activity are unprecedented during seasonal flu.
Almost all of the influenza viruses identified so far are 2009 H1N1 influenza A viruses. These viruses remain similar to the virus chosen for the 2009 H1N1 vaccine, and remain susceptible to the antiviral drugs oseltamivir and zanamivir with rare exception.
Last week the CDC reported that influenza activity increased dramatically in the U.S.
4,855 (37.5%) specimens tested by U.S. World Health Organization (WHO) and National Respiratory and Enteric Virus Surveillance System (NREVSS) collaborating laboratories and reported to CDC/Influenza Division were positive for influenza.
All subtyped influenza A viruses being reported to CDC were 2009 influenza A (H1N1) viruses.
The proportion of deaths attributed to pneumonia and influenza (P&I) was above the epidemic threshold.
Eleven influenza-associated pediatric deaths were reported. Nine of these deaths were associated with 2009 influenza A (H1N1) virus infection and two were associated with an influenza A virus for which subtype is undetermined.
The proportion of outpatient visits for influenza-like illness (ILI) was above the national baseline. All 10 regions reported ILI above region-specific baseline levels.
Forty-six states reported geographically widespread influenza activity, Guam and three states reported regional influenza activity, one state, the District of Columbia, and Puerto Rico reported local influenza activity, and the U.S. Virgin Islands did not report.
...
Companies with Potential Treatments for Swine Flu
CEL-SCI Corporation (Amex: CVM)
Product: LEAPS-H1N1
Currently Under Special
Fast Track Trials Authorized by FDA
...
Flu Stock Upturn? President Has Declared an H1N1 National Emergency
Written by Staff and Wire Reports
Saturday, 24 October 2009 07:56
http://biomedreports.com/articles/most-popular/14675-obama-declares-swine-flu-a-national-emergency-.html
President Barack Obama has declared the swine flu outbreak a national emergency. The White House on Saturday said Obama signed a proclamation that would allow medical officials to bypass certain federal requirements.
The declaration that Obama signed allows Health and Human Services chief Kathleen Sebelius to bypass federal rules when opening alternative care sites, such as offsite hospital centers at schools or community centers, if needed.
Hospitals could modify patient rules — for example, requiring them to give less information during a hectic time — to quicken access to treatment, with government approval.
The declaration, which the White House announced Saturday, allows HHS in some cases to let hospitals relocate emergency rooms offsite to reduce flu-related burdens and to protect noninfected patients.
Administration officials said the declaration was a pre-emptive move designed to make decisions easier when they need to be made. Officials said this was not in response to any single development on an outbreak that has lasted months and has killed more than 1,000 people in the United States.
It was the second of two steps needed to give Sebelius extraordinary powers during a crisis. On April 26, the administration declared swine flu a public health emergency, allowing the shipment of roughly 12 million doses of flu-fighting medications from a federal stockpile to states in case they eventually needed them. At the time, there were 20 confirmed cases in the U.S. of people recovering easily. There was no vaccine against swine flu, but the CDC had taken the initial step necessary for producing one.
"As a nation, we have prepared at all levels of government, and as individuals and communities, taking unprecedented steps to counter the emerging pandemic," Obama wrote in the declaration.
Because of vaccine production delays, the government has backed off initial, optimistic estimates that as many as 120 million doses would be available by mid-October. As of Wednesday, only 11 million doses had been shipped to health departments, doctor's offices and other providers, according to the Centers for Disease Control and Prevention officials said.
The government now hopes to have about 50 million doses of swine flu vaccine out by mid-November and 150 million in December.
The flu virus has to be grown in chicken eggs, and the yield hasn't been as high as was initially hoped, officials explained.
In Massachusetts, the Boston Globe is reporting that for the first time this fall, public health authorities described the state’s influenza outbreak as widespread, the highest category on the scale of disease spread. In a weekly surveillance report, officials said they had seen a “dramatic increase in influenza-like illnesses over the past few weeks’’ compared with early fall levels in previous years.
“We had always been predicting this,’’ Dr. Lauren Smith, medical director of the state Department of Public Health, said yesterday. “We knew the H1N1 [swine flu] virus was going to be increasing. We didn’t know when, but now we do. It’s here.’’
It was just six months ago that the U.S. Centers for Disease Control and Prevention reported that two children in California had developed a respiratory illness never before seen in humans, referring to the infection as "swine flu" in its Morbidity and Mortality Weekly Report.
Flu activity is now widespread in 46 states. Nationwide, visits to doctors for influenza-like-illness are increasing steeply and are now higher than what is seen at the peak of many regular flu seasons. In addition, flu-related hospitalizations and deaths continue to go up nation-wide and are above what is expected for this time of year.
Below is a summary of the most recent key indicators:
Visits to doctors for influenza-like illness (ILI) increased steeply since last week in the United States, and overall, are much higher than what is expected for this time of the year. ILI activity now is higher than what is seen during the peak of many regular flu seasons.
Total influenza hospitalization rates for laboratory-confirmed flu are climbing and are higher than expected for this time of year.
The proportion of deaths attributed to pneumonia and influenza (P&I) based on the 122 Cities Report has increased and has been higher than what is expected at this time of year for two weeks. In addition, 11 flu-related pediatric deaths were reported this week; 9 of these deaths were confirmed 2009 H1N1, and two were influenza A viruses, but were not subtyped. Since April 2009, CDC has received reports of 95 laboratory-confirmed pediatric 2009 H1N1 deaths and another 7 pediatric deaths that were laboratory confirmed as influenza, but where the flu virus subtype was not determined.
Forty-six states are reporting widespread influenza activity at this time. They are: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, and Wyoming. This many reports of widespread activity are unprecedented during seasonal flu.
Almost all of the influenza viruses identified so far are 2009 H1N1 influenza A viruses. These viruses remain similar to the virus chosen for the 2009 H1N1 vaccine, and remain susceptible to the antiviral drugs oseltamivir and zanamivir with rare exception.
Last week the CDC reported that influenza activity increased dramatically in the U.S.
4,855 (37.5%) specimens tested by U.S. World Health Organization (WHO) and National Respiratory and Enteric Virus Surveillance System (NREVSS) collaborating laboratories and reported to CDC/Influenza Division were positive for influenza.
All subtyped influenza A viruses being reported to CDC were 2009 influenza A (H1N1) viruses.
The proportion of deaths attributed to pneumonia and influenza (P&I) was above the epidemic threshold.
Eleven influenza-associated pediatric deaths were reported. Nine of these deaths were associated with 2009 influenza A (H1N1) virus infection and two were associated with an influenza A virus for which subtype is undetermined.
The proportion of outpatient visits for influenza-like illness (ILI) was above the national baseline. All 10 regions reported ILI above region-specific baseline levels.
Forty-six states reported geographically widespread influenza activity, Guam and three states reported regional influenza activity, one state, the District of Columbia, and Puerto Rico reported local influenza activity, and the U.S. Virgin Islands did not report.
Companies with Certified Existing Treatments for
Swine Flu
Gilead Sciences, Inc. (NASDAQ:GILD)
Roche Holding Ltd. (OTC:RHHBY)
Product: Tamiflu (oseltamivir)
GlaxoSmithKline plc (NYSE:GSK) /
Biota Holdings Ltd.(ASX:BTA)
Product: Relenza (zanamivir)
Baxter International Inc. (NYSE: BAX)
Product: A(H1N1) vaccine using its Vero cell culture technology
Novartis AG (NYSE:NVS)
Product: Influenza A(H1N1) vaccine using Cell-based manufacturing technology
BioCryst Pharmaceuticals,Inc. (NASDAQ:BCRX)
Product: Peramivir Intravenous
Sanofi-Aventis SA (NYSE:SNY)
Product: Swine Flu Vaccine
Companies with Potential Treatments for Swine Flu
CEL-SCI Corporation (Amex: CVM)
Product: LEAPS-H1N1
Currently Under Special
Fast Track Trials Authorized by FDA
Companies with Potential Vaccines
and Treatments for Swine Flu
Biota Holdings Ltd.(ASX:BTA) /
Daiichi Sankyo
Product: CS-8958
Novavax, Inc. (NASDAQ:NVAX)
Product: Swine Flu Vaccines
using Virus-like particle (VLP) technology
Inovio Biomedical Corporation (NYSE Amex:INO)
Product: SynCon™ H1N1 influenza DNA vaccines
Vical Incorporated(Public, NASDAQ:VICL)
Product: Patented DNA delivery technology
Sinovac Biotech Ltd. (Amex: SVA)
Product: Panflu(TM)
Wyeth (NYSE: WYE)
Product: PCV13 or Prevnar 13
MedImmune / AstraZeneca PLC (NYSE:AZN)
Product: needle-free, nasal spray swine flu vaccine by using Live Attenuated Influenza Vaccine (LAIV) technology
Companies with Adjuvants
for Swine Flu Vaccines
BioSante Pharmaceuticals, Inc.
(NASDAQ: BPAX)
Product: BioVant™ H1N1 adjuvant
Hemispherx Biopharma (AMEX:HEB)
Product: Ampligen
Antigenics, Inc. (NASDAQ:AGEN)
Product: QS-21 Stimulon
Other Technologies
Which Combat H1N1
Oculus Innovative Sciences, Inc.
(NASDAQ:OCLS)
Product: Microcyn®
Technology platform
Aethlon Medical, Inc. (OTC:AEMD)
Product: Hemopurifier®
BioCryst's investigational H1N1 drug granted Emergency Use OK
Written by Staff and Wire Reports
Saturday, 24 October 2009 03:51
http://biomedreports.com/articles/most-popular/14673-emergency-use-authorization-granted-for-biocrysts-peramivir.html
RxNews Recap for Friday 10-23-09
Written by Mary Davila
Saturday, 24 October 2009 06:28
Below is a list of the companies that made news in the healthcare sector for Friday October 23, 2009.
http://biomedreports.com/articles/most-popular/14674-rxnews-recap-for-friday-10-23-09.html
...ist nicht dein Ernst !??
Unilife Secures US$5.2m in Pennsylvania Job Creation Program Funds to Fuel Corporate Expansion
Oct 23, 2009 14:41 ET
http://www.marketwire.com/press-release/Unilife-Medical-Solutions-ASX-UNI-1064763.html
LEWISBERRY, PA--(Marketwire - October 23, 2009) - Unilife Medical Solutions Limited ("Unilife" or "the Company") (ASX: UNI) (PINKSHEETS: UNIFF) today announced it has accepted a US$5.2 million offer of assistance from the Commonwealth of Pennsylvania to support the creation of 241 new jobs within York County.
The offer of assistance from the Commonwealth of Pennsylvania accepted by Unilife includes access to the following programs:
-- An award of US$2 million for the development of a new facility in South-Central Pennsylvania under the Redevelopment Assistance Capital Program (RACP);
-- Up to US$2 million in low-interest financing loans for land and building acquisition and construction costs from the Pennsylvania Industrial Development Authority (PIDA);
-- A US$500,000 Opportunity Grant, which may be used for any eligible costs associated with a company project;
-- US$482,000 in Job Creation Tax Credits for the creation of 241 highly-skilled jobs by 2013, which can be applied to the Company's Pennsylvania Corporate Net Income Tax obligations; and
-- US$200,000 in Customised Job Training Grants, which reimburse 75% of eligible costs associated with advanced level training for new or existing employees.
These funds will be used to support Unilife's establishment as a US-based global leader in the design, development and supply of innovative safety medical devices for use within US and international pharmaceutical and healthcare markets. Over the last 12 months, Unilife has moved toward this goal by relocating key commercial and operational functions from Australia to its FDA-registered manufacturing facilities in Lewisberry, Pennsylvania. The Company has effectively doubled its size during this period with 87 staff now employed at its Lewisberry facility.
The Company recently announced steps to further accelerate its rate of business expansion within the United States, and, in particular, Central Pennsylvania. These expansion plans include the proposed redomiciliation of Unilife from Australia to the United States, listing of the Company on NASDAQ and the establishment of a major new global headquarters and manufacturing facility within Central Pennsylvania, which is evolving as a global centre for pharmaceutical and medical device development.
The RACP and PIDA funds committed from the Commonwealth will be used to develop the new Unilife facility in York County, Pennsylvania. The facility will support anticipated demand from pharmaceutical companies and other healthcare industry leaders for Unilife's range of ready-to-fill and clinical safety syringes, with production capacity of the ready-to-fill syringe expected to exceed 450 million units per year beyond 2014.
The 241 positions expected to be created at the facility will help drive this business expansion, and include a range of highly-skilled roles including the production, validation, marketing and supply of Unilife's current and pipeline products. Further information on the development of this new facility will be released by the Company upon the signing of the formal agreements with the selected developer.
Should the Pennsylvania General Assembly not pass a new Capital Budget Itemization Act by December 31, 2009, the US$2 million RACP award will be replaced by the provision of US$2 million over 10 years for business renovations under the Infrastructure and Facilities Improvement Program (IFIP).
Comments by Commonwealth of Pennsylvania Governor Ed Rendell
"Unilife's decision to expand its operations in York County is further proof that we can grow our economy and create good jobs and opportunities for our people if we're willing to invest in ourselves," said Governor Rendell. "Having a dynamic company of Unilife's caliber choose to locate their headquarters reflects well on our efforts and on the workforce in York County. It also illustrates the value in building partnerships and relationships outside of the U.S."
Comments by Unilife CEO Alan Shortall
Unilife's CEO, Alan Shortall, stated, "We are very pleased that the Commonwealth of Pennsylvania has chosen to offer Unilife this significant funding package that will help stimulate high-tech job creation and local investment during such challenging economic times. It is clear to me that the Pennsylvania government shares Unilife's vision, and has confidence in our ability to continue to deliver upon our business objectives and help the many millions of healthcare professionals and self-injecting individuals currently at risk of needlestick injuries and the blood borne viruses they can transmit.
"As an emerging global leader for innovative safety medical devices, we are committed to helping enhance the international credentials of Pennsylvania as a place for pharmaceutical and healthcare companies to do business.
"The funding program will help defray the initial costs and cash outlays required for the acquisition of our new facility and the automated production lines necessary to manufacture our products. We are fortunate to be working with a Government that displays the leadership and forward-thinking needed to support companies such as Unilife who are expanding their operations within Pennsylvania and providing vital job opportunities for highly-skilled individuals."
About Unilife
Unilife Medical Solutions Ltd is an ISO 13485 certified company that designs, develops and supplies innovative safety medical devices. Listed on the Australian Securities Exchange (ASX: UNI) since 2002, Unilife has FDA-registered manufacturing facilities in the US State of Pennsylvania and a proprietary portfolio of clinical and prefilled safety syringes designed for use within healthcare and pharmaceutical markets.
Shareholder / Analyst Enquiries:
Australia
Jeff Carter
Phone: + 61 2 8346 6500
United States
Stuart Fine
Phone: + 1 908 469 1788
ProLogis 2009 Earnings Call Transcript(s)
Q1
ProLogis, Q1 2009 Earnings Call Transcript
April 30, 2009
http://seekingalpha.com/article/134449-prologis-q1-2009-earnings-call-transcript?source=feed
Q2
ProLogis Q2 2009 Earnings Call Transcript
July 23, 2009
http://seekingalpha.com/article/150949-prologis-q2-2009-earnings-call-transcript
Q3
ProLogis Q3 2009 Earnings Call Transcript
October 22, 2009
http://seekingalpha.com/article/168310-prologis-q3-2009-earnings-call-transcript?source=feed
Unilife CEO Makes Open Market Purchase of $500,000 of Company Shares
Oct 23, 2009 09:09 ET
http://www.marketwire.com/press-release/Unilife-Medical-Solution-ASX-UNI-1064529.html
LEWISBERRY, PA--(Marketwire - October 23, 2009) - Unilife Medical Solutions Limited ("Unilife" or "the Company") (ASX: UNI) (PINKSHEETS: UNIFF) today announced that its Chief Executive Officer Alan Shortall has made open market purchases of Company shares.
The total number of shares purchased on October 21, 2009 was 479,800 at an average price of A$1.026 per share. Mr. Shortall has authorized his broker to purchase additional shares that will bring the total number of shares purchased this week to in excess of 500,000 shares.
Mr. Shortall said that he has elected to purchase these shares in the open market rather than participate in the recently announced private placement.
"The reason I chose to purchase these shares via the open market was to show our shareholders that I am standing by them in their belief in the Company," Mr. Shortall said.
"I could have simply participated in the private placement and obtained the shares at a discount to market and received the benefit of the same options that the institutions received, but I have instead chosen to show my allegiance to the Company and its shareholders by purchasing additional shares in the open market. I believe a direct market purchase is a truer reflection of my genuine support for our Company and my confidence in our long term prospects and world-class management team."
In considering his investment Mr. Shortall continued, "The progress the Company has made during the last two years, and our recent closing of the A$32.1 million private placement to institutional investors, provides me with the confidence to state that despite current economic conditions, I believe that Unilife has never been in a better position, operationally or financially."
About Unilife
Unilife Medical Solutions Ltd is an ISO 13485 certified company that designs, develops and supplies innovative safety medical devices. Listed on the Australian Securities Exchange (ASX: UNI) since 2002, Unilife has FDA registered manufacturing facilities in the US State of Pennsylvania and a proprietary portfolio of clinical and prefilled safety syringes designed for use within healthcare and pharmaceutical markets.
Shareholder / Analyst Enquiries:
Australia
Jeff Carter
Phone: + 61 2 8346 6500
United States
Stuart Fine
Phone: + 1 908 469 1788
ProLogis Q3 2009 Earnings Call Transcript
October 22, 2009
http://seekingalpha.com/article/168310-prologis-q3-2009-earnings-call-transcript?source=feed
ProLogis Reports Third Quarter 2009 Results
Date : 10/22/2009 @ 8:00AM
Source : PR Newswire
http://ih.advfn.com/p.php?pid=nmona&cb=1256302017&article=40011398&symbol=NY^PLD
***
ProLogis Posts 3Q Loss On More Write-Downs, Sees Steadiness
Date : 10/22/2009 @ 9:10AM
Source : Dow Jones News
http://ih.advfn.com/p.php?pid=nmona&cb=1256302017&article=40012984&symbol=NY^PLD
Pixantrone Produces High Rates of Complete Remission in Multiple Relapsed and Refractory Indolent and Aggressive Non-Hodgkin's L
Date : 10/22/2009 @ 1:30AM
Source : PR Newswire
Stock : (CTIC)
http://ih.advfn.com/p.php?pid=nmona&article=40002776&symbol=CTIC
Jiangbo Pharmaceuticals Announces Resignation of Chief Operating Officer
Date : 10/22/2009 @ 12:00PM
Source : PR Newswire
http://ih.advfn.com/p.php?pid=nmona&cb=1256227713&article=40016954&symbol=NB^JGBO
Jiangbo Pharmaceuticals Announces Resignation of Chief Operating Officer
LAIYANG, China, Oct. 22 /PRNewswire-Asia-FirstCall/ -- Jiangbo Pharmaceuticals, Inc. (OTC:JGBO) (BULLETIN BOARD: JGBO) (the "Company" or "Jiangbo"), a pharmaceutical company with its principal operations in China, today announced the resignation of Mr. Haibo Xu, the Company's Chief Operating Officer ("COO"), effective October 20, 2009. Mr. Xu resigned for health reasons. The Company has initiated a search for a replacement candidate for COO. Mr. Xu will continue in his role as a member of the Company's Board of Directors.
Mr. Wubo Cao, the Company's Chief Executive Officer, said, "We would like to thank Mr. Xu for all of his contributions as Jiangbo's COO and we look forward to continuing to work with him as a valued board member who is committed to maximizing the Company's future growth and shareholder value."
About Jiangbo Pharmaceuticals, Inc.
Jiangbo Pharmaceuticals is engaged in the research, development, production, marketing and sales of pharmaceutical products in China. The Company's operations are located in Eastern China in an Economic Development Zone in Laiyang City, Shandong Province. Jiangbo produces both western and Chinese herbal-based medical drugs in tablet, capsule, granule, syrup and electuary (sticky syrup) form. For additional information, please visit the Company's website ( http://www.jiangbopharma.com/ ).
Safe Harbor Statement
Certain statements in this press release that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements are not guarantees of future performance and are subject to risks and uncertainties that could cause the Company's actual results and financial position to differ materially from those included within the forward-looking statements. Forward-looking statements involve risks and uncertainties. Actual results may differ materially from anticipated or predicted results, and reported results should not be considered as an indication of future performance. The potential risks and uncertainties include, among others, the Company's ability to obtain raw materials needed in manufacturing, the continuing employment of key employees, the failure risks inherent in testing any new drug, the possibility that regulatory approvals may be delayed or become unavailable, patent or licensing concerns that may include litigation, direct competition from other manufacturers and product obsolescence. More information about the potential factors that could affect the Company's business and financial results is included in the Company's filings, available via the United States Securities and Exchange Commission.
For more information, please contact:
Jiangbo Pharmaceuticals, Inc.
Ms. Elsa Sung, CFO Phone: +1-954-727-8435 Email: Web: http://www.jiangbopharma.com/
CCG Investor Relations, Inc.
Mr. Crocker Coulson, President Phone: +1-646-213-1915 Email: Web: http://www.ccgirasia.com/
DATASOURCE: Jiangbo Pharmaceuticals, Inc.
CONTACT: Jiangbo Pharmaceuticals, Inc., Ms. Elsa Sung, CFO,
+1-954-727-8435, or ; Or CCG Investor Relations, Inc., Mr.
Crocker Coulson, President, +1-646-213-1915, or
Web site: http://www.jiangbopharma.com/
http://www.ccgirasia.com/
Novavax and Xcellerex Announce Collaboration to Develop Large-scale Manufacturing Process for 2009 H1N1 Influenza VLP Vaccine
Date : 10/21/2009 @ 7:30AM
Source : PR Newswire
Stock : Novavax (MM) (NVAX)
http://ih.advfn.com/p.php?pid=nmona&cb=1256139903&article=39988985&symbol=N^NVAX
Suntech Introduces Reliathon - Utility Solar Platform that Reduces Costs and Speeds Up Development of Utility Scale Projects Acr
Date : 10/21/2009 @ 8:00AM
Source : PR Newswire
http://ih.advfn.com/p.php?pid=nmona&cb=1256139903&article=39990635&symbol=NY^STP
Advanced Energy(R) and Suntech Announce Multi-Year Agreement for Solaron(R) Inverter Solutions
Date : 10/21/2009 @ 11:12AM
Source : PR Newswire
http://ih.advfn.com/p.php?pid=nmona&cb=1256139903&article=39995423&symbol=NY^STP
"shame" on you!
LOL
Unilife to Exhibit at Two Major Pharmaceutical Industry Events
Oct 21, 2009 10:04 ET
http://www.marketwire.com/press-release/Unilife-Medical-Solution-ASX-UNI-1063118.html
LEWISBERRY, PA--(Marketwire - October 21, 2009) - Unilife Medical Solutions Limited ("Unilife" or "the Company") (ASX: UNI) (PINKSHEETS: UNIFF) today announced it will be exhibiting at two upcoming pharmaceutical trade shows and conferences.
The Parenteral Drug Association (PDA) Universe of Pre-filled Syringes and Injection Devices, Conference and Exhibition takes place between October 27 and 30, 2009 in Venice, Italy. It is the pre-eminent annual gathering of pharmaceutical companies and device manufacturers on matters relating to prefillable injection systems for parenteral drug formulations. Unilife can be found at Booth E.
PharmaPack 2010 takes place February 1 and 2, 2010 in Paris, France. More than 200 companies will be exhibiting at PharmaPack, with over 2,200 people expected to attend including major decision-makers from pharmaceutical, biopharmaceutical and healthcare companies. Unilife will be exhibiting at Booth A34.
Unilife's proprietary portfolio of ready-to-fill glass and clinical safety syringes feature a unique automatic (passive) retraction mechanism which allows operators to control the speed of needle withdrawal directly from the body into the barrel of the syringe to help protect those at risk of needlestick injuries and other unsafe injection practices.
Unilife CEO Alan Shortall said the PDA Universe of Prefilled Syringes Conference to occur in Venice later this month would mark the first time that the Company and its products would be marketed at a landmark pharmaceutical industry event.
"We are especially proud of our representation at PDA Venice, as the event symbolises the launch of our Company onto the pharmaceutical stage for parenteral drug delivery devices. We anticipate a good reception for our range of safety syringes, with meetings being scheduled with a number of pharmaceutical companies and other interested parties."
Pharmaceutical companies and other interested parties seeking to schedule a meeting with Unilife at these upcoming events are asked to contact Mark Hassett, Director of Sales and Marketing at +1 619 993 9810 or mark.hassett@unilife.com.
About Unilife
Unilife Medical Solutions Ltd is an ISO 13485 certified company that designs, develops and supplies innovative safety medical devices. Listed on the Australian Securities Exchange (ASX : UNI) since 2002, Unilife has FDA-registered manufacturing facilities in the US State of Pennsylvania and a proprietary portfolio of clinical and prefilled safety syringes designed for use within healthcare and pharmaceutical markets.
Shareholder / Analyst Enquiries:
Australia
Jeff Carter
Phone: + 61 2 8346 6500
United States
Stuart Fine
Phone: + 1 908 469 1788
_bbb_: need a rocket for my german board!
you have some ???
NeoMedia and Scanbuy Reach Settlement and License Agreement
Date : 10/20/2009 @ 12:38PM
Source : Business Wire
Stock : NeoMedia Technologies, Inc. (NEOM)
http://ih.advfn.com/p.php?pid=nmona&cb=1256058071&article=39976782&symbol=NB^NEOM
$$$$$$$$$ (edit €€€€€€€€€) - come to 0815ax
Raser Technologies Receives Invitation to the White House to Participate in U.S. Clean Energy Forum
20.10.2009 18:04
http://www.finanznachrichten.de/nachrichten-2009-10/15245989-raser-technologies-receives-invitation-to-the-white-house-to-participate-in-u-s-clean-energy-forum-004.htm
U.S. Secretary of Commerce Gary Locke Invites Richard Clayton to Discuss Opportunities and Challenges in the Clean Energy Economy
Raser Technologies, Inc. (NYSE: RZ), an energy technology company, announced today that U.S. Secretary of Commerce Gary Locke has invited Raser Principal Executive Officer Richard Clayton to participate in a forum titled ”Clean Energy Economy.”
”It’s an honor to be invited to such a small, select group to discuss and offer views about the future of clean energy in the United States. I believe as the only baseload renewable energy, geothermal power could have a huge impact on the future of clean energy in this country,” said Richard Clayton.
”Ensuring American competitiveness in the clean energy economy is critical to our economic recovery today and to our economic growth tomorrow,” Secretary of Commerce Gary Locke said in the invitation to the forum.
The forum is scheduled for October 22, 2009 in Washington, D.C.
The American Recovery and Reinvestment Act passed earlier this year sets aside millions of dollars in grants and billions in loan guarantees to support and advance renewable energy projects.
”The federal government and many state governments are putting a lot of money behind renewable energy,” said Clayton. ”They recognize that clean energy will be a significant part of our country’s economy and energy security.”
Raser has applied for several innovative exploration grants through the Department of Energy’s Geothermal Technologies Program and also intends on applying for the 30% Treasury Grant for its current and future power plants as well as loan guarantees for its Lightning Dock, New Mexico project and others.
Raser Technologies commissioned its first geothermal power plant in April of this year. That plant, located in southern Utah, now delivers clean, renewable energy to Anaheim, Calif. Raser has plans to build additional plants in Utah, New Mexico, Nevada and Oregon.
About Raser Technologies
Raser (NYSE: RZ) is an environmental energy technology company focused on geothermal power development and technology licensing. Raser’s Power Systems segment is seeking to develop clean, renewable geothermal electric power plants and bottom-cycling operations, incorporating licensed heat transfer technology. Raser’s Transportation and Industrial segment focuses on extended-range plug-in-hybrid vehicle solutions and using Raser’s award-winning Symetron™ technology to improve the torque density and efficiency of the electric motors and drive systems used in electric and hybrid-electric vehicle powertrains and industrial applications. Further information on Raser may be found at: www.rasertech.com.
Contacts:
Raser Technologies, Inc.
Issa Arnita, 801-765-1200
Investor Relations
investorrelations@rasertech.com
or
Hayden IR
Cameron Donahue, 651-653-1854
cameron@haydenir.com
© 2009 Business Wire
52wk Range: 0.27 - 6.63
c: 5.83
Trading Review for Sunrise Senior Living Inc. Issued by StockPreacher.com
* Press Release
* Source: StockPreacher
* On 6:50 am EDT, Tuesday October 20, 2009
http://finance.yahoo.com/news/Trading-Review-for-Sunrise-pz-534268787.html?x=0&.v=1
H1N1 Program is "Moving So Fast"
Written by M.E.Garza
Tuesday, 20 October 2009 00:00
http://biomedreports.com/articles/most-popular/13910-h1n1-program-is-qmoving-so-fastq.html