BLUE BELL, Pa., Sept. 13, 2011 /PRNewswire/ -- Inovio Pharmaceuticals, Inc. (NYSE Amex: INO), a leader in the development of therapeutic and preventive vaccines against cancers and infectious diseases, announced today that early data from a Phase I study assessing its PENNVAX™-G global HIV vaccine plus a virus vector vaccine, Modified Vaccinia Ankara-Chiang Mai Double Recombinant (MVA-CMDR), as a unique prime-boost preventive HIV vaccination strategy has demonstrated strong immune responses and safety. These results were presented at the AIDS Vaccine Conference in Bangkok, Thailand. This interim data was from the first cohort of 11 healthy subjects enrolled in the US as part of the first phase of the study to assess safety of the prime-boost combination vaccine. Enrollment will now continue in three sites in Africa in the next phase of the study.
The National Institute of Allergy and Infectious Diseases (NIAID), part of the U.S. National Institutes of Health (NIH), is sponsoring this randomized, open label trial Phase I study, called RV262, which will enroll 92 total participants and is designed to assess safety and immune responses. The study is being conducted by the U.S. Military HIV Research Program (MHRP) through its clinical research network in the US and Africa. This clinical trial was designed to test safety and immunogenicity of a unique heterologous DNA/recombinant poxvirus prime-boost preventive HIV immunization strategy aimed at global coverage. Together the vaccines are designed to deliver a diverse mixture of antigens for HIV-1 subtypes A, B, C, D and E.
Volunteers were given a priming immunization with Inovio's PENNVAX™-G synthetic consensus immunogen at months 0 and 1, followed by boosting with MVA-CMDR at months 3 and 6. Immunomonitoring was performed at pre-immunization and at two weeks post-DNA and MVA immunizations, respectively.
Early analysis of this initial data revealed a strong cell-mediated immune response, with CD4+ and CD8+ T cells specific for both the gag and env antigens encoded by the prime and boost agents. Significantly, anti-env CD4+ T-cell immune responses were noted in 100% (11 of 11) of evaluated subjects and CD8+ T-cell responses were noted in 45% (5 of 11) of evaluated subjects after the first MVA boost following the two DNA vaccinations. The env specific CD4+ and CD8+ T-cell response rates were noted to be 73% (8 of 11) and 45% (5 of 11) respectively after the second MVA boost.
Dr. J. Joseph Kim, Inovio's President and CEO, said: "We are pleased to see the response rate and magnitude of T-cell responses generated by the prime-boost vaccine combination. We believe that a 100% vaccine induced env-specific T-cell immune response result has not been achieved in previous HIV vaccine clinical trials. We look forward to completing and receiving the full data set from this study."
About Inovio's PENNVAX™-G and CELLECTRA® Electroporation System
PENNVAX™-G is a SynCon® multi-subtype optimized synthetic immunogen. Based on a consensus of env and gag antigens of HIV-1 global subtypes A, C, D, this synthetically created immunogen is intended to provide broad antibody and T-cell immune responses to target many divergent strains of this challenging disease. Inovio's electroporation systems have been shown to increase immune responses to a DNA-based immunogen by a 100 times or more and have been shown to be safe and well-tolerated in multiple human studies. Inovio's SynCon® immunogens against cervical dysplasias and cancer as well as HIV Clade B (both delivered using the CELLECTRA® electroporation device), have previously achieved best-in-class T-cell immune responses, which are thought to be important in controlling HIV infection and transmission.
The U.S Military HIV Research Program (MHRP)—centered at Walter Reed Army Institute of Research (WRAIR) and part of the US Medical Research and Materiel Command—conducts research to develop an effective HIV vaccine and integrates prevention, treatment, diagnosis and monitoring as part of an international effort to protect troops and reduce the risk of HIV infection worldwide. MHRP has developed five state-of-the-art international research sites in the U.S., Africa and Asia. The program collaborates on HIV prevention care and treatment services, funded by the President's Emergency Plan for AIDS Relief (PEPFAR), with African militaries and in the communities where it conducts research.
In 2009, MHRP announced results of an Army-sponsored clinical trial in Thailand that demonstrated for the first time a modest ability to protect against HIV infection, reducing the number of infections by 31.2 percent. MHRP researchers are now working with scientists around the world, with the support of NIAID, to dissect the trial results to inform basic research and design future clinical trials to translate this scientific milestone into a deployable vaccine. For more information, visit www.hivresearch.org.
About Inovio Pharmaceuticals, Inc.
Inovio is developing its revolutionary synthetic immunogen technology to extend the profound medical benefits of the 20th century's immune-system-stimulating vaccines by preventing and treating today's cancers and challenging infectious diseases. Its SynCon® immunogens are designed to provide broad cross-strain protection against known as well as newly emergent unmatched strains of pathogens such as influenza. These immunogens, in combination with Inovio's proprietary CELLECTRA® delivery method, have been shown in humans to be safe and generate best-in-class immune responses. Inovio's clinical programs include Phase II studies for cervical dysplasia/cancer, leukemia and hepatitis C virus and Phase I studies for influenza and HIV. Partners and collaborators include the University of Pennsylvania, Merck, ChronTech, National Cancer Institute, U.S. Military HIV Research Program, NIH, HIV Vaccines Trial Network, University of Southampton, and PATH Malaria Vaccine Initiative. More information is available at www.inovio.com.
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This press release contains certain forward-looking statements relating to our business, including our plans to develop electroporation-based drug and gene delivery technologies and DNA vaccines and our capital resources. Actual events or results may differ from the expectations set forth herein as a result of a number of factors, including uncertainties inherent in pre-clinical studies, clinical trials and product development programs (including, but not limited to, the fact that pre-clinical and clinical results referenced in this release may not be indicative of results achievable in other trials or for other indications, that the studies or trials may not be successful or achieve the results desired, that results from one study may not necessarily be reflected or supported by the results of other similar studies and that results from an animal study may not be indicative of results achievable in human studies), the availability of funding to support continuing research and studies in an effort to prove safety and efficacy of electroporation technology as a delivery mechanism or develop viable DNA vaccines, the adequacy of our capital resources, the availability or potential availability of alternative therapies or treatments for the conditions targeted by the company or its collaborators, including alternatives that may be more efficacious or cost-effective than any therapy or treatment that the company and its collaborators hope to develop, evaluation of potential opportunities, issues involving product liability, issues involving patents and whether they or licenses to them will provide the company with meaningful protection from others using the covered technologies, whether such proprietary rights are enforceable or defensible or infringe or allegedly infringe on rights of others or can withstand claims of invalidity and whether the company can finance or devote other significant resources that may be necessary to prosecute, protect or defend them, the level of corporate expenditures, assessments of the company's technology by potential corporate or other partners or collaborators, capital market conditions, our ability to successfully integrate Inovio and VGX Pharmaceuticals, the impact of government healthcare proposals and other factors set forth in our Annual Report on Form 10-K for the year ended December 31, 2010, our Form 10-Q for the three months ended June 30, 2011, and other regulatory filings from time to time. There can be no assurance that any product in Inovio's pipeline will be successfully developed or manufactured, that final results of clinical studies will be supportive of regulatory approvals required to market licensed products, or that any of the forward-looking information provided herein will be proven accurate.
SOURCE Inovio Pharmaceuticals, Inc.