{"id":53773,"date":"2012-10-08T14:24:41","date_gmt":"2012-10-08T14:24:41","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/genetic-immunity-receives-gmp-certification-for-in-house-manufacturing-facility.php"},"modified":"2012-10-08T14:24:41","modified_gmt":"2012-10-08T14:24:41","slug":"genetic-immunity-receives-gmp-certification-for-in-house-manufacturing-facility","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/genetic-immunity-receives-gmp-certification-for-in-house-manufacturing-facility.php","title":{"rendered":"Genetic Immunity Receives GMP Certification for In-House Manufacturing Facility"},"content":{"rendered":"<p><p>    BUDAPEST, HUNGARY--(Marketwire - Oct 8, 2012) - Genetic    Immunity (OTCBB: PWRV) is pleased to announce    the GMP approval of its manufacturing facility. The development    of the GMP manufacturing process and the facility was financed    from a $4 million grant received from the Hungarian Office for    Innovation and Technology.  <\/p>\n<p>    \"To establish a GMP manufacturing facility is a major milestone    for Genetic Immunity. Initially, it will serve our need to    produce high quality ingredients to our nanomedicine products    tested in clinical trials. We developed our GMP manufacturing    technology and processes to be suitable to upgrade them to a    commercial scale. This approval demonstrates the capability of    our team to advance our DermaVir HIV-specific immunotherapy to    the market, and our new candidate products from the bench to    the bedside,\"said Dr. Julianna Lisziewicz, CEO of Genetic    Immunity.  <\/p>\n<p>    The GMP status is provided for the manufacturing and the    validated quality control processes of the Active    Pharmaceutical Ingredient of our immunotherapeutic nanomedicine    products.Genetic Immunity has a state of the art R&D    laboratory that includes a dedicated GMP facility. Due to the    platform feature of our plasmid DNA based nanomedicine    technology, only the nucleotide sequence of the DNA is specific    for the target disease. Consequently, the manufacturing and the    quality control process of the lead and all pipeline products    is the same. This means that the GMP facility can be used for    the manufacturing all products of Genetic Immunity regardless    of clinical stage. The common GMP manufacturing technology    simplifies the regulatory process, saves costs and time in    clinical development, and reduces time to market approval of    medicinal products.  <\/p>\n<p>    \"With this GMP facility we have successfully closed the    manufacturing gap between clinical trial scale and the    commercial production. With continuous development of the    manufacturing processes we are able to control the costs and    achieve a competitive price for each market segments at an    attractive ROI ratio for every product. We are strongly focused    on the market and are well prepared for large scale    manufacturing for our planned Expanded Access program of    DermaVir,\" said Mr. Viktor Rozsnyay, CEO of Power of the Dream    Ventures.  <\/p>\n<p>    Genetic Immunity is a wholly owned subsidiary of Power of the    Dream Ventures, Inc. (OTCBB: PWRV).  <\/p>\n<p>    About Genetic Immunity Genetic Immunity is    part of Power of the Dream Ventures, Inc. (PWRV) committed to    bring innovative Hungarian products and services to public.    GeneticImmunity is a clinical stage technology company    committed to discovering, developing, manufacturing and    commercializing a new class of immunotherapeutic biologic drugs    for the treatment of viral infections, cancer and allergy. The    Company's two distinguished technology platforms will    revolutionize the treatment of these chronic diseases. Our    Langerhans cell targeting nanomedicines are exceptional in both    safety and immune modulating activity boosting specific    Th1-type central memory T cells. Such immune responses differ    from antibodies induced by vaccines. These are essential to    eliminate infected cells or cancerous cells, and balance the    immune reactivity in response to allergens. Our IT team    generated a complex algorithm to match the mechanism of action    of our drugs with clinical efficacy. In the future, we will    predict the clinical and immunological benefits of our drugs    based on the patient's disease and genomic background. The    unique mixture of our technologies represents the next    generation of personalized but not individualized medicines    ensuring a longer and higher economic return. Genetic    Immunity's primary focus is the development of DermaVir that    acts to boost the immune system of HIV-infected people to    eliminate the infected cells that remained in the reservoirs    after successful antiretroviral treatment. Three clinical    trials conducted in EU and US showed that DermaVir    immunizations were as safe as placebo and only four sequential    patch treatments were required to reduce the HIV infected cells    in the blood within 24 weeks.  <\/p>\n<p>    In 1988 Drs. Lisziewicz and Lori founded the Genetic Immunity    in the US after they described the 1st patient whose    immune system was boosted to control HIV after treatment    interruption (Lisziewicz et al. New England Journal of Medicine    1999) that lead to the invention of DermaVir. The Company's    innovative technology team directed by Dr. Lisziewicz, a    champion of immune busting therapies, is now headquartered in    Budapest (Hungary). For more information please visit     <a href=\"http:\/\/www.geneticimmunity.com\" rel=\"nofollow\">http:\/\/www.geneticimmunity.com<\/a>  <\/p>\n<p>    Forward-looking statements Statements    in this press release that are not strictly historical in    nature constitute forward-looking statements qualified in their    entirety by this cautionary statement. Forward-looking    statements include, without limitation, statements regarding    business combination and similar transactions, prospective    performance and opportunities and the outlook for the    companies' businesses, including, without limitation, the    ability of PWRV to advance Genetic Immunity's product pipeline    or develop a curative immunotherapy for HIV, performance and    opportunities and regulatory approvals, the anticipated timing    of data from clinical data; the possibility of unfavorable    results of the company's clinical trials; filings and approvals    relating to the transaction; the expected timing of the    completion of the transaction; the ability to complete the    transaction considering the various closing conditions; and any    assumptions underlying any of the foregoing. Investors are    cautioned that any such forward-looking statements are not    guarantees of future performance and involve risks and    uncertainties and are cautioned not to place undue reliance on    these forward-looking statements. Actual results may differ    materially from those currently anticipated due to a number of    risks and uncertainties. All forward-looking statements are    based on information currently available to the companies, and    the companies assume no obligation to update any such    forward-looking statements.  <\/p>\n<\/p>\n<p>View post: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.marketwire.com\/mw\/release.do?id=1710138&amp;sourceType=3\" title=\"Genetic Immunity Receives GMP Certification for In-House Manufacturing Facility\">Genetic Immunity Receives GMP Certification for In-House Manufacturing Facility<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> BUDAPEST, HUNGARY--(Marketwire - Oct 8, 2012) - Genetic Immunity (OTCBB: PWRV) is pleased to announce the GMP approval of its manufacturing facility. The development of the GMP manufacturing process and the facility was financed from a $4 million grant received from the Hungarian Office for Innovation and Technology <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/genetic-immunity-receives-gmp-certification-for-in-house-manufacturing-facility.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[5],"tags":[],"class_list":["post-53773","post","type-post","status-publish","format-standard","hentry","category-genetic-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/53773"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=53773"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/53773\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=53773"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=53773"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=53773"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}