{"id":113402,"date":"2010-06-01T12:29:15","date_gmt":"2010-06-01T16:29:15","guid":{"rendered":"https:\/\/www.send2press.com\/wire\/advanced-phase-i-and-phase-ii-studies-of-targeted-gene-delivery-confirm-that-rexin-g-impacts-survival-in-chemotherapy-resistant-bone-and-soft-tissue-sarcoma-asco-2010\/"},"modified":"2010-06-01T12:29:15","modified_gmt":"2010-06-01T16:29:15","slug":"advanced-phase-i-and-phase-ii-studies-of-targeted-gene-delivery-confirm-that-rexin-g-impacts-survival-in-chemotherapy-resistant-bone-and-soft-tissue-sarcoma-asco-2010","status":"publish","type":"post","link":"https:\/\/www.send2press.com\/wire\/advanced-phase-i-and-phase-ii-studies-of-targeted-gene-delivery-confirm-that-rexin-g-impacts-survival-in-chemotherapy-resistant-bone-and-soft-tissue-sarcoma-asco-2010\/","title":{"rendered":"Advanced Phase I and Phase II Studies of Targeted Gene Delivery Confirm That Rexin-G Impacts Survival in Chemotherapy-resistant Bone and Soft Tissue Sarcoma (ASCO 2010)"},"content":{"rendered":"<p class=\"s2pred\"><strong>NEWS SOURCE: Epeius Biotechnologies Corporation<\/strong><\/p>\n<p>SAN MARINO, Calif., June 1 (SEND2PRESS NEWSWIRE) &#8212; Epeius Biotechnologies Corporation (<a href=\"http:\/\/www.epeiusbiotech.com\" target=\"_blank\" rel=\"noopener\">www.epeiusbiotech.com<\/a>) today announces the results of the clinical trial entitled &#8220;Advanced Phase I\/II Evaluation of Tumor-Targeted Gene Delivery: Intravenous Rexin-G as Stand Alone Therapy for Chemotherapy-resistant Bone and Soft Tissue Sarcoma&#8221; at the ASCO Annual Meeting on June 8, 2010. The presentation will be discussed by Dr. Kristen N. Ganjoo, Stanford University Medical Center, Palo Alto CA.<\/p>\n<p> STUDY SUMMARY: The goals of the study were to evaluate the over-all safety and efficacy of intravenous infusions of Rexin-G, a tumor-targeted retrovector bearing a cytocidal anti-cyclin G1 construct, in chemo-therapy-resistant bone and soft tissue sarcoma. A Phase II &#8220;run-in&#8221; component was integrated by adaptive design by continuing treatment if the patient had Grade 1 or less toxicity.<\/p>\n<p> Thirty-six patients received escalating doses of Rexin-G intravenously three times a week for four weeks. Analysis of safety showed no dose-limiting toxicity and no cumulative toxicity in patients treated with Rexin-G monotherapy for up to 2 years.<\/p>\n<p> Analysis of efficacy revealed a dose-dependent relationship between progression-free survival\/overall survival and Rexin-G dosage (p = 0.02 and 0.002 respectively) which was significant at the 5% statistical level by the log-rank test. Median survival was 11.5 months and one-year survival was 40% in the high-dose groups.<\/p>\n<p> These findings indicate that intravenous Rexin-G is safe and well-tolerated with no cumulative toxicity, and that Rexin-G controls tumor growth, and prolongs progression-free survival and over-all survival times in a dose-dependent manner in patients with chemotherapy resistant bone and soft tissue sarcoma. <\/p>\n<p> <strong>About Epeius Biotechnologies:<\/strong><br \/> Epeius Biotechnologies Corporation (<a href=\"http:\/\/www.epeiusbiotech.com\" target=\"_blank\" rel=\"noopener\">www.epeiusbiotech.com<\/a>) is a privately held biopharmaceutical company dedicated to the advancement of genetic medicine with the development and commercialization of its lead products, Rexin-G and Reximmune-C, and its high-performance gene delivery systems.<\/p>\n<p> To learn more about these agents and\/or ongoing clinical trials, please contact Dr. Erlinda M. Gordon at egordon_@_epeiusbiotech.com.<\/p>\n<p>News issued by: Epeius Biotechnologies Corporation<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/www.send2press.com\/wire\/images\/10-0504-epeiusbio_72dpi.jpg\" width=\"500\" height=\"375\" alt=\"Epeius Biotechnologies Corporation\"\/><\/p>\n<p><small>Original Image: <a href=\"https:\/\/www.send2press.com\/wire\/images\/10-0504-epeiusbio_72dpi.jpg\" class=\"autohyperlink\" rel=\"nofollow\">https:\/\/www.send2press.com\/wire\/images\/10-0504-epeiusbio_72dpi.jpg<\/a><\/small><\/p>\n<p> # # # <\/p>\n<p><small>Original Story ID:  (5980) :: 2010-06-0601-002<\/small><\/p>\n<p><small>Original Keywords: Epeius Biotechnologies Corporation, clinical trial, Advanced Phase I\/II Evaluation of Tumor-Targeted Gene Delivery, Intravenous Rexin-G as Stand Alone Therapy for Chemotherapy-resistant Bone and Soft Tissue Sarcoma, at the ASCO Annual Meeting Epeius Biotechnologies Corporation San Marino California SAN MARINO, Calif.<\/small><\/p>\n<p><small>Alternate Headline: ASCO 2010: Studies of Targeted Gene Delivery Confirm That Rexin-G Impacts Survival in Chemotherapy-resistant Bone and Soft Tissue Sarcoma<\/small><\/p>\n<p><small><strong>NEWS ARCHIVE NOTE:<\/strong> this archival news content, issued by the news source via Send2Press Newswire, was originally located in the Send2Press&reg; 2004-2015 2.0 news platform and has been permanently converted\/moved (and redirected) into our 3.0 platform. Also note the story &#8220;reads&#8221; counter (bottom of page) does not include any data prior to Oct. 30, 2016. This press release was originally published\/issued: Tue, 01 Jun 2010 12:29:15 +0000<\/p>\n<p><\/small><\/p>\n<p class=\"s2pred\"><strong>NEWS SOURCE: Epeius Biotechnologies Corporation<\/strong> | Published: 2010-06-01 12:29:15<\/p>\n","protected":false},"excerpt":{"rendered":"<p>SAN MARINO, Calif. (SEND2PRESS NEWSWIRE) &#8212; Epeius Biotechnologies Corporation today announces the results of the clinical trial entitled &#8216;Advanced Phase I\/II Evaluation of Tumor-Targeted Gene Delivery: Intravenous Rexin-G as Stand Alone Therapy for Chemotherapy-resistant Bone and Soft Tissue Sarcoma&#8217; at the ASCO Annual Meeting on June 8, 2010. The presentation will be discussed by Dr. Kristen N. Ganjoo, Stanford University Medical Center, Palo Alto CA.<\/p>\n","protected":false},"author":9780,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"singles-wide.php","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[19937],"tags":[],"class_list":["post-113402","post","type-post","status-publish","format-standard","hentry","category-press-releases-archive","has-post-title","has-post-date","no-post-category","no-post-tag","no-post-comment","has-post-author"],"acf":[],"views":427,"_links":{"self":[{"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/posts\/113402","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/users\/9780"}],"replies":[{"embeddable":true,"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/comments?post=113402"}],"version-history":[{"count":0,"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/posts\/113402\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/media?parent=113402"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/categories?post=113402"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.send2press.com\/wire\/wp-json\/wp\/v2\/tags?post=113402"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}