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Inovio Pharmaceuticals Reports 2011 Second Quarter Financial Results
Date:8/8/2011

prime-boost vaccination strategy against genotype 1 hepatitis C virus (HCV) in a Phase I clinical study. Inovio will contribute its electroporation delivery technology to this collaboration. Clinical study costs will be shared equally by the collaborators.

Subsequent to the quarter, Inovio announced it had expanded its existing license agreement with the University of Pennsylvania, adding exclusive worldwide licenses for technology and intellectual property for novel DNA vaccines against prostate cancer, CMV (cytomegalovirus), malaria, hepatitis B, RSV (respiratory syncytial virus), and MRSA (methicillin-resistant staphylococcus aureus). The amendment also encompasses a new optimized IL-12 cytokine gene adjuvant.

Clinical DevelopmentInovio reported that 91% of evaluated patients (10 of 11) that had received three vaccinations of VGX-3100, its therapeutic SynCon® cervical dysplasia/cancer DNA vaccine delivered using intramuscular electroporation, displayed strong and persistent memory T-cell responses at month nine (six months after the last vaccination). Inovio subsequently reported long-term durability of T cell immune responses of up to two years (at the latest time measured) in 7 of 8 evaluated patients following a fourth vaccination of VGX-3100. This data further highlights the viability of using multiple booster vaccinations with a DNA vaccine delivered using electroporation, in contrast to other non-replicating vaccine vectors that may induce unwanted immune responses against the vector after multiple vaccinations.

Inovio is continuing to set up sites and enroll patients for its

SOURCE Inovio Pharmaceuticals, Inc.
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