smiler o
- 21 Sep 2006 09:16
- 147 of 1180
Thanks for that, ref the mail I sent you they have changed today : )
potatohead
- 22 Sep 2006 13:41
- 150 of 1180
more news next week guys, I am hopeing its the news on colonical cancer
smiler o
- 22 Sep 2006 13:44
- 151 of 1180
OK PH will be watching, where have you been, on holiday ??
smiler o
- 25 Sep 2006 16:49
- 153 of 1180
Driver
Strange, I keep watching this share more than the others, could make some good money on this 1p would be a good start ! : )
potatohead
- 25 Sep 2006 17:07
- 154 of 1180
no not on holiday.. just letting you guys get on with it, news out this week, gonna be huge.. massive..
almost falic like
potatohead
- 26 Sep 2006 12:53
- 156 of 1180
September 26, 2006 07:03 AM Eastern Time
Alnylam Grants Quark a License to Develop and Commercialize
Two RNAi Therapeutic Products
Target-Specific Licenses for RNAi Intellectual Property Granted Under Alnylams InterfeRx Program -
BIOWIRE2K
CAMBRIDGE, Mass. & FREMONT, Calif.--(BUSINESS WIRE)--Alnylam Pharmaceuticals, Inc. (Nasdaq:ALNY), a leading RNAi therapeutics company, announced today that it has granted Quark Biotech, Inc. InterfeRx licenses to discover, develop, and commercialize RNAi therapeutics targeting the p53 and RTP801 genes for certain diseases. Quark has filed investigational new drug (IND) applications for RNAi therapeutics for both targets, in the case of p53 for the treatment of renal failure, and in the case of RTP801 for the treatment of ocular diseases, specifically macular degeneration. Detailed financial terms were not disclosed, but include upfront, annual, and milestone payments, as well as royalties on sales of any products covered by the licensing agreements. Simultaneously, Quark has agreed to withdraw its support of opposition to the Kreutzer-Limmer patent series currently granted in Europe.
We are very pleased to provide Quark with a license to Alnylam intellectual property for its innovative RNAi therapeutic programs, said John Maraganore, Ph.D., President and Chief Executive Officer of Alnylam. With these two licenses, we have now granted six InterfeRx licenses to date, and 12 licenses in total for therapeutic RNAi applications. With the recent strengthening of our patent estate, we expect that companies working in the area of RNAi therapeutics will continue to seek licenses to our intellectual property. In fact, we anticipate that into next year, a significant number of clinical-stage RNAi therapeutic programs will be licensed under Alnylam intellectual property.
RNAi therapeutics represent a promising approach as a new class of drugs for unmet medical needs wherever the disease targets are otherwise practically un-druggable with todays medicines, said Dr. Daniel Zurr, Chief Executive Officer of Quark. Quarks creative way to discover new targets and concepts for treatment of devastating diseases, combined with an RNAi approach, have yielded very encouraging early results with our p53 and RTP801 drugs. We are dedicated to help society with innovative medicines by moving from novel gene targets to unique compounds and eventually commercial products. In our comprehensive review of the intellectual property landscape for the commercialization of RNAi therapeutics, it was clear that a license to Alnylam patents is required for these exciting programs, and were pleased to have access to these assets.
Alnylam has built a leading portfolio of issued or granted patents in the worlds major pharmaceutical markets that broadly claim fundamental features for all RNAi therapeutics, including the structural and functional properties of synthetic RNAi therapeutic products. The recognized potential of RNAi to provide the basis for an entirely new class of drugs to treat a broad range of human diseases has created a high level of interest among biopharmaceutical companies in gaining access to this intellectual property. Alnylam created the InterfeRx licensing program to grant licenses under this intellectual property to biotechnology and pharmaceutical companies wishing to pursue RNAi therapeutics against specific targets outside Alnylams core strategic interests. In addition to Quark, Alnylams InterfeRx licensees include Calando Pharmaceuticals, Nastech Pharmaceutical Company, GeneCare Research Institute Co., and, under an option agreement, Benitec Ltd.
Quarks RNAi therapeutic that specifically targets p53 is being developed to reduce tubular damage and preserve kidney function. The novel concept of the temporary and reversible inhibition of p53 to prevent apoptosis in normal cells following ischemia-reperfusion injury was first described by Quark in 1999 in the journal Science [Science 285, 1733-37 (1999)] and is covered by broad issued U.S. patents. Extensive animal studies have shown that the drug protects the animals from ischemia/reperfusion-induced acute kidney injury.
Quarks second RNAi therapeutic targets the gene RTP801. Quark reported the discovery of RTP801 in 2002 and was granted several U.S. patents covering the gene, its encoded protein and their inhibition to treat serious diseases. The inhibition of the RTP801 target has been shown to have beneficial effect in a number of oxidative (hypoxic) injuryrelated disease models. Extensive animal studies have shown that the drug protects the animals from the three hallmarks of macular degeneration: retinal neuronal death, blood vessel regeneration, and vascular leakiness.
About RNA Interference (RNAi)
RNA interference, or RNAi, is a naturally occurring mechanism within cells for selectively silencing and regulating specific genes. Since many diseases are caused by the inappropriate activity of specific genes, the ability to silence genes selectively through RNAi could provide a new way to treat a wide range of human diseases. RNAi is induced by small, double-stranded RNA molecules. One method to activate RNAi is with chemically synthesized small interfering RNAs, or siRNAs, which are double-stranded RNAs that are targeted to a specific disease-associated gene. The siRNA molecules are used by the natural RNAi machinery in cells to cause highly targeted gene silencing.
About Alnylam
Alnylam is a biopharmaceutical company developing novel therapeutics based on RNA interference, or RNAi. The company is applying its therapeutic expertise in RNAi to address significant medical needs, many of which cannot effectively be addressed with small molecules or antibodies, the current major classes of drugs. Alnylam is building a pipeline of RNAi therapeutics; its lead program is in Phase I human clinical trials for the treatment of respiratory syncytial virus (RSV) infection, which is the leading cause of hospitalization in infants in the U.S. The companys leadership position in fundamental patents, technology, and know-how relating to RNAi has enabled it to form major alliances with leading companies including Merck, Medtronic, Novartis, and Biogen Idec. The company, founded in 2002, maintains global headquarters in Cambridge, Massachusetts, and has an additional operating unit in Kulmbach, Germany. Alnylam is honored to be the emerging/mid-cap company recipient of the 2006 James D. Watson Helix Award, the biotechnology industrys award for outstanding achievement. For more information, visit www.alnylam.com.
About Alnylam Intellectual Property (IP)
Alnylams IP estate includes issued or granted fundamental patents in the worlds major pharmaceutical markets that claim the broad structural and functional properties of synthetic RNAi therapeutic products. As it applies to the U.S. and Europe, these include:
The Tuschl II 704 patent (U.S. Patent No. 7,056,704) issued in June 2006, which broadly covers methods of making siRNAs to silence any and all disease targets;
The Tuschl II 196 patent (U.S. Patent No. 7,078,196) issued in July 2006, which broadly covers methods of making siRNAs with or without chemical modifications;
The Kreutzer-Limmer I 623 patent (EP 1144623) granted in August 2002, and upheld in June 2006, covering methods, medicaments, and uses of siRNAs having, among other structural features, a length of 15-21 base pairs;
The Kreutzer-Limmer I 945 patent (EP 1214945) granted in June 2005, covering compositions, methods, and uses of siRNAs with a length between 15 and 49 nucleotides;
Additional fundamental patents and patent applications licensed to Alnylam on an exclusive or non-exclusive basis, including those of Crooke (U.S. Patent Nos. 5,898,031 and 6,107,094), Fire and Mello (U.S. Patent No. 6,506,559), and Glover et al. (EP 1230375); and,
Several divisional patent applications pending of the aforementioned issued or granted patents and additional patent applications pending including Tuschl I.
In addition, Alnylam has a broad worldwide license for RNAi therapeutics from Isis Pharmaceuticals, Inc. for more than 150 issued patents pertaining to specific chemical modification of oligonucleotides used to introduce drug-like properties in siRNAs. These include:
Phosphorothioate and 2'-O-methyl modifications (Buhr, U.S. Patent No. 6,476,205); and,
2'-Fluoro modifications (Cook, U.S. Patent Nos. 5,670,633; 6,005,087; and 6,531,584).
Alnylam invites interested licensees to view issued or granted claims for these and other key Alnylam patents at www.alnylam.com/patent-estate.
About Quark
Quark Biotech, Inc. is a privately held development-stage, biopharmaceutical company headquartered in Fremont, California. Through innovative combination of gene silencing and DNA microarray technology, Quark has pioneered and patented its BiFARTM platform for high-throughput functional profiling, allowing significant advances in the identification of target genes and proteins. This technology allows the company to develop conceptually novel drugs that provide previously unavailable benefits to patients. Quark is currently investigating novel targets identified using this enabling foundation technology. Quark has focused development efforts on treatment of fibrotic and ischemic diseases of the eye, kidney and lungs, in indications with clear unmet medical needs. Quark corporate product development teams and research facilities are based in Fremont with additional research facilities in Ness-Ziona, Israel. Additional information is available at www.quarkbiotech.com.
smiler o
- 26 Sep 2006 16:42
- 157 of 1180
Driver
away again tomorrow till 0700 to 2000 so bound to get some news ! just my luck
smiler o
- 26 Sep 2006 17:21
- 159 of 1180
Driver
whats all that crap ph has posted is it anything to do with erx ??
potatohead
- 27 Sep 2006 09:58
- 163 of 1180
EXPECT NEWS THIS WEEK.. TODAY OR TOMORROW BY MY RECKONING
Article Preview
Researchers' data from the United Kingdom, Germany and United States advance cancer treatment research
Vaccine Weekly - Sep. 13, 2006
2006 SEP 13 - (NewsRx.com) -- Data on cancer treatment are outlined in reports from the United Kingdom, Germany and United States.
Study 1: A new anticancer glycolipid monoclonal antibody, SC104, directly induces tumor cell apoptosis.
According to recent research from England, "A novel monoclonal antibody was raised by immunization of mice with colorectal tumor cell lines. The fusion was screened by immunohistochemistry for binding to primary colorectal tumors. Subsequent analysis on primary disaggregated colorectal tumors show that the antibody recognizes a cell surface antigen expressed by the majority of colorectal tumors."
"Antigen characterization has shown that the antibody ...
http://www.therapeuticsdaily.com/news/article.cfm?contentValue=1078531&contentType=sentryarticle&channelID=28
EIRX THERAPEUTICS PLC ("EIRX")
POTENTIAL NEW THERAPIES FOR COLORECTAL & OTHER CANCERS
Cork, Ireland, 10th January, 2006 EiRx Therapeutics plc (AIM: ERX), the drug discovery company developing targeted therapies for cancer, is pleased to announce the filing of patent applications describing a novel class of drug candidates with potential value as treatments for a range of cancers including colorectal and breast tumours. This class of molecule is structurally dissimilar to the class of molecules for which patent applications were made in August 2005, thus ensuring a deeper pipeline of development for the treatment of colorectal and breast cancer.
Exploiting the insight afforded to them through their ALIBITM genomics platform, EiRx scientists developed EnPADTM technology to target APC-b-catenin signalling, a cellular control pathway known to play a major role in the majority of cases of colorectal cancer, as well as in several other tumour types. A custom-designed EnPADTM cell line was used to screen a focused library of drug-like, kinase inhibitor compounds, resulting in the discovery of a series of related compounds with selective activity against transformed cell types including colorectal and breast cancer cell lines. The EnPADTM technology development programme was funded in part by the Marie Curie Transfer Of Knowledge grant.
Commenting on the discovery, EiRxs Chief Scientific Officer Prof Tom Cotter said: The company's EnPADTM technology has again proven its ability to identify novel classes of molecules with selective biological activity. The class of molecules filed in the current patent applications are structurally quite different to those that were the subject of the earlier patent applications in August 2005. As a result we are in the enviable position of moving two chemical scaffolds through preclinical with the potential to treat these socio-economically important diseases.
EiRx Chairman John Pool said: Not only does filing a second class of molecule with activity against colorectal and breast cancer endorse our EnPADTM approach in drug discovery; it also demonstrates that EiRx has set its sights firmly on the identification and development of novel molecules to treat cancer. Having two series of molecules in preclinical development, both with the potential to treat colorectal and breast cancer, demonstrates that EiRx has the potential to rapidly become a key player in these very considerable therapeutic markets.
laurie squash
- 27 Sep 2006 10:52
- 164 of 1180
Someone has just sold 40 million shares.
potatohead
- 27 Sep 2006 14:05
- 165 of 1180
it was a broker to broker you numbskull, news coming..
potatohead
- 27 Sep 2006 14:20
- 166 of 1180
40mil buy just gone through now