AVI BioPharma and Cook Group Enter into License Agreement
to Develop NEUGENE Drugs for Vascular Diseases

Cook to fund all clinical development of three products for cardiovascular restenosis and develop products for peripheral vascular diseases

PORTLAND, Ore. - Mar. 13, 2006 - AVI BioPharma, Inc. (Nasdaq: AVII), today announced that it has entered into agreements with Cook Group Incorporated (Cook) for Cook's development and commercialization of products for vascular diseases. Cook has specifically licensed AVI's NEUGENE® antisense technology for down-regulating c-myc gene expression in the field of cardiovascular disease. Cook will take over clinical development of AVI's device-related programs for cardiovascular restenosis, including its Resten-NG® drug eluting stent (DES) program, Resten-MP™ microparticle delivery program and its new program for catheter delivery of Resten-NG.

Cook will fully fund the development, clinical, and regulatory costs of these programs in the US and Europe leading to commercialization. This funding is expected to result in expenditures by Cook that could reach $100 million.

Cook has also entered into a supply agreement to purchase the drugs for development, clinical studies, and commercialization from AVI. Because of the drugs' established Phase II clinical efficacy, AVI has forgone certain near term milestone payments in favor of a double-digit royalty on worldwide product sales and a commercialization milestone. Cook will purchase 692,003 shares of AVI common stock for $5 million under a stock purchase agreement. Cook will also take over AVI's facilities and personnel at its Colorado site. Additional terms of the agreements are not disclosed.

"Based upon promising Phase II clinical data in combating cardiovascular restenosis, and progress in our drug eluting stent and Resten-MP programs, AVI has now partnered its device-related cardiovascular programs with one of the preeminent vascular device companies in the world today," said Denis R. Burger, Ph.D., chief executive officer of AVI. "Together, Cook's device expertise and AVI's antisense technology become a formidable combination to address vascular diseases on many fronts. AVI will now narrow its internal cardiovascular focus exclusively to its coronary artery bypass graft (CABG) program that is moving into Phase II clinical trials later this year. Importantly, this agreement also frees up resources for AVI to move more aggressively in its infectious disease program focusing on hHepatitis C and influenza A, including avian influenza (H5N1)."

Resten-NG (AVI-4126) is a third-generation antisense agent that targets the key regulatory gene involved in cardiovascular restenosis, the transcription factor referred to as c-myc. It is believed to regulate the many downstream genes that produce the pathology of restenosis, namely cell migration and adhesion, collagen formation, secretion of extra-cellular matrix, and cell proliferation, among others. The c-myc gene expression is immediately activated by the injury to the vascular lining during angioplasty and stent placement and peaks at 24 to 48 hours before subsiding. NEUGENE antisense drugs are particularly suited to prevent this process because they can be delivered immediately following injury to the angioplasty site by a variety of means including catheter and stent elution, or by systemic delivery using AVI's microparticle delivery system, Resten-MP™.

"Based upon our preliminary investigation, we believe that the Resten NG (AVI-4126) has great potential for use on drug eluting stents to reduce restenosis of stented vessels," said Bill Cook, founder of Cook Group Incorporated. "AVI's NeuGene antisense drug therapies also have potential to treat stenotic vessels systemically via catheter. Our company is honored to be a partner with AVI in the exploration of new, antisense vascular therapies."

Joseph B. Horn, AVI vice president of cardiology, who joined AVI from Cook a little over a year ago, will be re-joining Cook to advance these programs through clinical development and into commercialization. Horn spent eight years as president and CEO for Global Therapeutics, a medical device company that he founded and which was acquired by Cook in 1998. While at Cook, Horn was responsible for the introduction and sales of Cook products in Europe and South America. In addition, Horn worked with Cook medical researchers and physicians in the management of clinical studies of new medical devices.

"Joe's extensive experience and industry knowledge provides us with great confidence that our joint development program is in good hands at Cook," said Alan Timmins, president and chief operating officer of AVI. "We expect that Joe will not only be instrumental in bringing the licensed technology into commercialization but also open new applications for us to jointly pursue."

"I'm thrilled to be rejoining Cook with the team I've assembled to complete the mission that I started at AVI in the field of cardiology in the near term, and in all areas of vascular medicine in the longer term," Horn said. "Moving AVI's cardiovascular program forward in both Europe and the United States will be my initial priority, and I'm pleased to be surrounded by a talented team of professionals with cutting-edge technology to apply clinically. I believe this is a win-win scenario for both companies"

About Cook Group
The world's largest privately held manufacturer of medical devices with international headquarters in Bloomington, Ind., COOK® (www.cookmedical.com) is a leading designer, manufacturer and global distributor of minimally invasive medical device technology for diagnostic and therapeutic procedures. Since its founding in 1963, Cook has created innovative technologies for drug-eluting and bare metal stents, aortic and vascular endografts, catheters, wire guides, introducer needles and sheaths, embolization coils, medical biomaterials and contract manufacturing of biopharmaceuticals, vena cava filters and other minimally invasive medical devices for radiology, cardiology, urology and OB/GYN, critical care medicine, surgery, gastroenterology, bone access and endovascular therapies.

About AVI BioPharma
AVI BioPharma develops therapeutic products for the treatment of life-threatening diseases using third-generation NEUGENE antisense drugs. AVI's lead NEUGENE antisense compound is designed to target cell proliferation disorders, including cardiovascular restenosis, cancer and polycystic kidney disease. In addition to targeting specific genes in the body, AVI's antiviral program uses NEUGENE antisense compounds to combat disease by targeting single-stranded RNA viruses, including hepatitis C virus, influenza A virus, dengue virus, West Nile virus and Ebola virus. AVI has introduced a NEUGENE-based exon-skipping technology called ESPRIT therapy. 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 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 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.

MEDIA CONTACT:
David McCarty
Director of Public Relations
Cook Incorporated - 812-339-2235 ext. 2387
Email: dmccarty@cook-inc.com

Michael Hubbard (hubbard@avibio.com)
AVI BioPharma, Inc.
(503) 227-0554

Jenny Moede (jmoede@waggeneredstrom.com)
Waggener Edstrom Worldwide
Bioscience and Healthcare Practice
(503) 443-7000

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