AVI BioPharma Announces 2006 Second Quarter Financial Results Conference Call.

PORTLAND, Ore. -- AVI BioPharma, Inc. (Nasdaq:AVII) today announced that the company will hold a conference call to discuss its 2006 second quarter financial results on Tuesday, August 8, 2006, at 11:00 a.m. Eastern Time (8:00 a.m. Pacific Time).

Individuals interested in listening to the live conference call may do so by dialing [phone] toll free within the United States and Canada, or [phone] for international callers. A telephone replay of the conference call will be available for 48 hours beginning August 8 within two hours after the conclusion of the call, by dialing [phone] domestically or [phone] internationally, and entering reservation number 3161072.

The conference call can be heard live via audio webcast at the company's Web site: www.avibio.com. A replay will also be available for 14 days.

About AVI BioPharma

AVI BioPharma develops therapeutic products for the treatment of life-threatening diseases using third-generation NEUGENE(R) 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, West Nile virus, dengue 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.