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To: Robert Rose who wrote (95624)3/6/2000 11:18:00 AM
From: H James Morris  Respond to of 164684
 
As fast as my Carlsbad baby Isip. I love genes and small caps.
>
CARLSBAD, Calif., March 6 /PRNewswire/ -- Isis Pharmaceuticals (Nasdaq: ISIP) announced today that it has received issuance of U.S. patents on antisense inhibitors to 20 genes over the last two months. These gene inhibition patents are a result of Isis' highly productive rapid throughput screening program and computer assisted patenting system. These patents cover the use of antisense inhibitors against genes involved in several areas of disease including inflammatory responses, signal transduction processes, apoptosis, drug resistance and cancer, and other important areas of biology. Utilizing its proprietary technology, Isis has the ability to create and file patents on potent and selective antisense inhibitors to all 100,000 genes within the human genome. These antisense gene inhibitors have the potential to be drugs as well as a genomics tool within Isis' target validation program.

Isis' gene functionalization program helps solve a fundamental issue facing the pharmaceutical industry: how to determine which of the many novel gene targets available are most valuable to pursue for drug discovery. Isis' program uses antisense inhibitors together with other tools to understand the role each gene plays in a disease process. This information provides pharmaceutical companies with a fast and efficient way of prioritizing their proprietary genes and creating therapeutic value from their genomics efforts.

Targets covered in Isis' recently issued patents include gene inhibitors for inflammatory responses (LFA-3, TNFR-1, PLA-2), signal transduction processes (C-rel, SMAD, protein kinase-c), apoptosis (BCL-2 related proteins, IAP family members, Rip-1, Fadd), drug resistance and cancer (MDR, Jun-N- terminal Kinase Kinase-1).

In the last year alone, Isis has been issued more than 60 patents on antisense gene inhibitors. These patents, along with its earlier patents on gene inhibitors, make Isis one of the top ten holders of gene patents in the US. In addition, Isis holds more than 600 issued and allowed patents worldwide covering antisense inhibitors of genes, chemistries, and manufacturing as well as gene functionalization process.

Isis' target validation and gene functionalization program has the ability to identify antisense inhibitors to numerous genes per week and simultaneously produce patent applications on these gene inhibitors. To date, Isis has been successful in optimizing inhibitors to over 500 genes. The speed and efficiency of this program has attracted partnerships with companies such as Abbott, Aventis (formerly Rhone Poulenc-Rorer) and AstraZeneca.

"The issuance of this many patents related to such important genes in such a small period of time is evidence of the remarkable productivity and innovation of Isis' target validation program and its rapid identification process," said C. Frank Bennett, Vice President of Biology. "These patents provide further demonstration of the versatility and efficiency of antisense gene functionalization and target validation, a big step in converting genes into drugs."

"These patents contribute to Isis' large proprietary patent estate and show the increasing value of antisense in both the drug discovery effort and as a tool for genomics," said B. Lynne Parshall, Executive Vice President and CFO. "We will continue to aggressively patent in key areas including gene inhibition in order to further increase our dominant position in this novel technology."

This press release contains forward-looking statements concerning Isis' proprietary patent estate and its programs in target validation and gene functionalization. Such statements are subject to certain risks and uncertainties, particularly those inherent in the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics. Actual results could differ materially from those projected in this release. As a result, the reader is cautioned not to rely on these forward-looking statements. These and other risks concerning the Isis' patent estate and drug development programs are described in additional detail in Isis' Annual Report on Form 10-K/A for the year ended December 31, 1998, which is on file with the U.S. Securities and Exchange Commission, copies of which are available from the company.

Isis Pharmaceuticals, based in northern San Diego County, is engaged in the discovery and development of novel human therapeutic drugs. The company's first product, Vitravene(TM) (fomivirsen), to treat CMV-induced retinitis in AIDS patients, is being sold in the United States, Europe, Brazil and Switzerland. In addition, Isis has five compounds in human clinical trials: a Phase II study of ISIS 2302 for the prevention of renal transplant rejection is near completion, Phase II studies with an enema formulation for ulcerative colitis and a topical formulation for psoriasis are just beginning, and an aerosol administration for asthma is being explored. In addition, Isis has three anticancer compounds: ISIS 3521, ISIS 5132 and ISIS 2503, in Phase II studies and ISIS 14803 for the treatment of Hepatitis C is in a Phase I/II trial. The company also has several additional compounds in preclinical development. Isis' broad and proprietary patent estate of over 600 issued and allowed patents worldwide and has been recognized as one of the top ten holdings of gene patents issued in the U.S. In addition, Isis has created two divisions focused on more broadly capitalizing on Isis' expertise in RNA. Ibis Therapeutics, is a division focused on the discovery of small molecules that bind to RNA. Isis also has developed a target validation program aimed at utilizing antisense to assist the pharmaceutical industry in validating and prioritizing potential gene targets.

Vitravene(TM) is a trademark of Novartis AG.

SOURCE Isis Pharmaceuticals



To: Robert Rose who wrote (95624)3/6/2000 11:28:00 AM
From: Slumdog  Read Replies (1) | Respond to of 164684
 
Message 12996566



To: Robert Rose who wrote (95624)3/6/2000 12:49:00 PM
From: H James Morris  Read Replies (2) | Respond to of 164684
 
Robert, here's a Seattle based Bio-tech that's doing well.
Bought it this morning @ 30.
>SEATTLE--(BUSINESS WIRE)--March 6, 2000--

Results published in the Proceedings

of the National Academy of Sciences

NeoRx Corporation (Nasdaq:NERX) today announced publication of a peer-reviewed manuscript in the Proceedings of the National Academy of Sciences, reporting that a single dose of its proprietary Pretarget(R) technology cured established human lung (10/10 animals), colon (10/10 animals) and breast cancers (8/10 animals) implanted in mice. To be judged a cure, both complete disappearance of the tumor and absence of any re-growth for at least one year were required. These results were achieved with a single dose of radioactivity developed with NeoRx's proprietary Pretarget(R) technology. The manuscript appears in the February 15, 2000 issue of the journal.

"The key finding in these experiments was the ability to actually cure large, established tumors using the higher doses of radiation that can be safely administered with our Pretarget(R) technology," said Don Axworthy, NeoRx scientist and lead author on the paper. "Unlike other therapies that have been reported to be curative in animals, Pretarget(R) effected cures with only a single administration. We are looking forward to testing our latest Pretarget(R) therapy, with the incorporation of various improvements we have made since the original animal studies were done, in the clinic later this year."

In the manuscript, NeoRx scientists compared Pretarget(R) technology to the conventional targeting approach used by others. With Pretarget(R), the targeting antibody and radiation are injected separately and at different times, and join at tumor sites where the antibody has pre-localized. Radiation that does not join the antibody is rapidly eliminated from the body. This brief exposure of normal organs permits higher doses than the conventional approach to be administered safely, as has been shown in these animal trials and in patients. By contrast, the conventional approach links the radiation (a small drug) to the large antibody molecule, irradiating normal tissues such as bone marrow as it circulates for prolonged periods in the blood. Doses using the conventional approach are limited by normal organ exposure.

"Several groups have products under development using the conventional approach to radiotherapy," said Paul G. Abrams, M.D., J.D., NeoRx's chief executive officer. "We expect to begin formal Phase I trials with at least one Pretarget(R) product this year. Using a prototype Pretarget(R) product in patients with lymphoma, we have already observed 3 complete remissions (two of which occurred in patients who had progressed after high dose therapy and stem cell transplantation) in the 7 patients treated. As in the animal studies reported in our manuscript, these responses were observed after a single dose of Pretarget(R) Moreover, we began our clinical study at a dose higher than the maximum tolerated dose of conventional radiotherapy products, yet we did not see any clinically significant toxicity"

NeoRx recently announced the receipt of a grant from the National Cancer Institute that could total $950,000 to assist in bringing its Pretarget(R) Lymphoma product to the clinic. The Company owns or has in-licensed the basic Pretarget(R) patents (approved in the US, Canada, Europe and Japan) and has an additional 25 issued or allowed US patents in Pretarget(R).