SOURCE: AVI BioPharma, Inc.

December 23, 2008 08:00 ET

AVI BioPharma Strengthens Its Patent Position in RNA Therapeutics

Composition of Matter Patent for Enhanced Antisense Agent AVI-5126

PORTLAND, OR--(Marketwire - December 23, 2008) - AVI BioPharma, Inc. (NASDAQ: AVII), a developer of RNA-based drugs, today announced issuance of a U.S. patent protecting the composition of matter of its RNA-based therapeutic agent AVI-5126. The patent "Compositions for Enhancing Transport of Molecules Into Cells" (U.S. Patent No. 7,468,418) claims compositions and methods for AVI-5126, a PPMO (peptide-conjugated morpholino phosphorodiamidate oligomer)-based RNA therapeutic agent aimed at silencing C-MYC, an important protein in wound healing, cell proliferation and cancer.

AVI has licensed AVI-5126 to Global Therapeutics, a Cook Medical company, which is conducting the world's first clinical trial of a third generation drug-eluting stent ("DES") that uses an RNA-based therapeutic agent. AVI-5126 targets C-MYC, a key regulatory gene involved in cardiovascular restenosis, silencing the gene before the biochemical pathways leading to restenosis are fully triggered. The enhanced antisense compound has increased potency and bioavailability compared with earlier analogs, allowing for a DES system that delivers a lower concentration of more potent drug.

"This is a significant patent issuance for a number of AVI programs, but most importantly it covers the lead drug candidate on which Cook's Global Therapeutics unit is working," said Leslie Hudson, Ph.D., President and Chief Executive Officer of AVI. "This patent protects the broad concept of a cell delivery peptide that is conjugated to a neutral oligomer and its issuance significantly expands AVI's intellectual property base for the next generation of therapeutic oligomers capable of significantly improved bioavailability and potency."

AVI has published numerous articles in 2008 on novel compounds using the principle of peptide-PMO (PPMO) conjugates.

  --  Morpholino Oligomers Targeting the PB1 and NP Genes Enhance Survival
      of Mice Infected with Highly Pathogenic Influenza A H7N7 Virus
      Gabriel G, Nordman A, Stein DA, Iversen PL and Klend HD
      April 2008, The Journal of General Virology

  --  Inhibition of Iinfluenza A H3N8 Virus Infections in Mice by
      Morpholino Oligomers
      Lupfer C, Stein DA, Mourich DV, Tepper SE, Iversen PL and Pastey M
      March 28, 2008, Archives of Virology

  --  Inhibition of Alphavirus Infection in Cell Culture and in Mice with
      Antisense Morpholino Oliogmers
      Paessler S, Rijnbrand R, Stein DA, Ni H, Yun NE, Dziuba N,
      Borisevich V, Seregin A, Ma Y, Blouch R, Iversen PL, and Zacks MA
      July 5, 2008, Virology

  --  Inhibition of Multiple Species of Picornavirus Using a Morpholino
      Oligomer Targeting Highly Conserved IRES Sequence
      Stone J, Stein DA, Rijnbrand R, Iversen PL and Andino R
      June 2008, Antimicrobial Agents Chemotherapy

  --  Inhibition of Respiratory Syncitial Virus Infections with Morpholino
      Oligomers in Cell Cultures and in Mice
      Lai SH, Stein DA, Liao SL, Guerrero-Plata A, Hong C, Iversen PL,
      Casola A and Garofalo RP
      June 2008, Molecular Therapy

  --  Treatment of AG129 Mice with Antisense Morpholino Oligomers Increases
      Survival Time Following Challenge with Dengue 2 Virus
      Stein DA, Huang CYH, Silengo S, Amantana A, Crumley S, Blouch RE,
      Iversen, PL and Kinney RM
      September 2008, Journal of Antimicrobial Chemotherapy

  --  Delivery of Steric Block Morpholino Oligomers by (R-X-R)4 Peptides:
      Structure-activity Studies
      Abes R, Moulton HM, Clair P, Yang ST, Abes S, Melikov K, Prevot P,
      Youngblood DS, Iversen PL, Chernomordik LV and Lebleu B
      November 2008, Nucleic Acids Research

About AVI BioPharma

AVI BioPharma is focused on the discovery and development of RNA-based drugs utilizing proprietary derivatives of its antisense chemistry (morpholino-modified phosphorodiamidate oligomers or PMOs) that can be applied to a wide range of diseases and genetic disorders through several distinct mechanisms of action. Unlike other RNA therapeutic approaches, AVI's antisense technology has been used to directly target both messenger RNA (mRNA) and its precursor (pre-mRNA), allowing for both up- and down-regulation of targeted genes and proteins. AVI's RNA-based drug programs are being evaluated for the treatment of Duchenne muscular dystrophy as well as for the treatment of cardiovascular restenosis through our partner Global Therapeutics, a Cook Group Company. AVI's antiviral programs have demonstrated promising outcomes in Ebola Zaire and Marburg Musoke virus infections and may prove applicable to other viral targets such as HCV or Dengue viruses. For more information, visit

"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.

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