More significant NERX news: SAN DIEGO--(BUSINESS WIRE)--Dec. 13, 1999--NeoRx Corporation (Nasdaq:NERX.O) today announced that its scientists have successfully produced in bacteria a "fusion protein" intended for use in the Company's Pretarget Lymphoma product. The fusion protein comprises the binding portion of an anti-CD20 antibody genetically linked to streptavidin. The fusion protein is secreted at high concentration and spontaneously forms a tetramer with four binding sites for antigen and four binding sites for biotin, the ligand for streptavidin. The work was described by Dr. Yukang Lin, Ph.D. of NeoRx's Molecular Biology Group, at the Antibody Engineering Conference in San Diego. "The fusion protein is intended to replace the CD20/streptavidin chemical conjugate that we evaluated earlier this year in a Phase I safety study in patients with non-Hodgkins' lymphoma," said Karen Auditore-Hargreaves, Ph.D., NeoRx's Vice President of Research and Development. "The new construct not only provides a cost-effective, simplified process for production, but in animal models it also has shown superior targeting and pharmacokinetic characteristics to the chemical conjugate. Pretarget technology itself provides about a 5-fold improvement relative to conventional radioimmunotherapy in the tumor-to-blood ratio, a commonly used measure of targeting specificity. When chemical conjugate is replaced with fusion protein, we see a further 5-fold improvement, suggesting that ultimately we will be able to deliver safely previously unachievable doses of radiation to the patient." Pretarget technology involves decoupling of the targeting molecule from administration of the cytotoxic effector agent. Because the cytotoxic agent is a small radioactive molecule, it clears rapidly from the blood, reducing exposure of non-tumor tissues. This is in contrast to conventional radioimmunotherapy in which the targeting molecule and the radiation are administered as a single large complex that circulates for along time, all the while exposing non-tumor tissue to its cytotoxic effects. Pretarget technology has resulted in objective tumor responses, including complete responses in a Phase I trial in patients with lymphoma. NeoRx holds an exclusive license to patents covering fusion proteins with streptavidin for use in pretargeting. The Company plans to evaluate a fusion protein in clinical trials in the future. NeoRx Corporation is developing innovative products designed to provide improved, cost-effective treatments for patients with cancer.
This release contains forward-looking statements relating to the development of the company's products and future operating results that are subject to certain risks and uncertainties that could cause actual results to differ materially from those projected. The words "believe," "expect," "intend," "anticipate," variations of such words, and similar expressions identify forward-looking statements, but their absence does not mean that the statement is not forward-looking. These statements are not guarantees of future performance and are subject to certain risks, uncertainties and assumptions that are difficult to predict. Factors that could affect the company's actual result include the progress and costs of clinical trials and the timing of regulatory approvals. Reference is made to the company's latest Annual Report on Form 10-K filed with the Securities and Exchange Commission for a more detailed description of such factors. Readers are cautioned not to place undue reliance on these forward-looking statements that speak only as of the date of this release. The Company undertakes no obligation to publicly update any forward-looking statement to reflect new information, events or circumstances after the date of this release or to reflect the occurrence of unanticipated events.
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NeoRx and Pretarget are registered trademarks of NeoRx Corporation in the United States and/or foreign countries. (c) 1999 NeoRx Corporation. All Rights Reserved.
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CONTACT: NeoRx Corporation Melinda Kile, 206/286-2508 Controller neorx.com
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