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AVI BioPharma Announces Termination of Cardiovascular Agreement With Medtronic; AVI Continues Further Development of Resten-NG in Several Areas.


PORTLAND, Ore. -- AVI BioPharma, Inc. (Nasdaq:AVII) today announced the termination of its license agreement with Medtronic Inc. for the delivery of AVI's antisense therapy Resten-NG(R) via devices, including stents and catheters, in cardiovascular disease Cardiovascular disease
Disease that affects the heart and blood vessels.

Mentioned in: Lipoproteins Test

cardiovascular disease 
. AVI (Audio Video Interleaved) A Windows multimedia video format from Microsoft. It interleaves standard waveform audio and digital video frames (bitmaps) to provide reduced animation at 15 fps at 160x120x8 resolution. Audio is 11,025Hz, 8-bit samples.  and Medtronic first entered into an agreement to develop Resten-NG for stent and catheter delivery in 2001, and modified the agreement in September 2003. AVI regains full exclusive rights to development of Resten-NG in all cardiovascular applications, including device delivery.

"Our cardiovascular program is moving forward on several levels, including evaluating the delivery of Resten-NG using our proprietary microparticle delivery system," said Denis Denis, king of Portugal: see Diniz.  R. Burger, Ph.D., chief executive officer at AVI.

Resten-NG works by inhibiting c-myc expression, a major contributor to the pathology that the company believes leads to restenosis following an angioplasty procedure. This third-generation antisense antisense, DNA or RNA manipulated in a laboratory so that its components (nucleotides) form a complementary copy of normal, or "sense," messenger RNA (mRNA; see nucleic acid).  compound has been successfully delivered using three methods: systemically with a microparticle preparation, locally via a drug-delivery catheter, or as a drug coating on stents.

In August 2003, AVI initiated a Phase II clinical study to evaluate efficacy and safety of Resten-NG delivered systemically with AVI's microparticle preparation, compared with angioplasty and stent placement alone. Successful systemic delivery of Resten-NG could make the drug available for broad application with stent placement and for multiple applications after angioplasty.

About AVI BioPharma

AVI BioPharma develops therapeutic products for the treatment of life-threatening diseases using two technology platforms: third-generation NEUGENE(R) antisense drugs and cancer immunotherapy. AVI's lead NEUGENE antisense compound is designed to target cell proliferation disorders, including cardiovascular restenosis, cancer and polycystic kidney disease Polycystic Kidney Disease Definition

Polycystic kidney disease (PKD) is one of the most common of all life-threatening human genetic disorders.
. In addition to targeting specific genes in the body, AVI's antiviral program uses NEUGENE antisense compounds to target single-stranded RNA viruses RNA viruses,
n See viruses.
, including West Nile virus West Nile virus, microorganism and the infection resulting from it, which typically produces no symptoms or a flulike condition. The virus is a flavivirus and is related to a number of viruses that cause encephalitis. , SARS coronavirus, calicivirus and hepatitis C. AVI's second technology, AVICINE(R), is a therapeutic cancer vaccine with late-stage trials planned for the treatment of pancreatic cancer. More information about AVI is available on the company's Web site at http://www.avibio.com/.

"Safe Harbor" Statement under the Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and  of 1995: The statements that are not historical facts contained in this release are forward-looking statements that involve risks and uncertainties, including, but not limited to, the results of research and development efforts, the results of preclinical and clinical testing, the effect of regulation by the FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
 and other agencies, the impact of competitive products, product development, commercialization and technological difficulties, and other risks detailed in the company's Securities and Exchange Commission filings.
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Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:Business Wire
Geographic Code:1USA
Date:Jun 30, 2004
Words:408
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