{"id":19200,"date":"2023-06-05T11:12:00","date_gmt":"2023-06-05T11:12:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4119408_AE19408_0"},"modified":"2023-06-05T11:12:00","modified_gmt":"2023-06-05T11:12:00","slug":"sirnaomics-reports-interim-results-of-stp705-phase-i-clinical-study-for-medical-aesthetics-treatment-in-adults-undergoing-abdominoplasty","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=19200","title":{"rendered":"Sirnaomics Reports Interim Results of STP705 Phase I Clinical Study for Medical Aesthetics Treatment in Adults Undergoing Abdominoplasty"},"content":{"rendered":"<p><span class=\"xn-location\">HONG KONG<\/span>, GERMANTOWN,&nbsp;Md. and SUZHOU,&nbsp;China, <span class=\"xn-chron\">June 5, 2023<\/span> \/PRNewswire\/ &#8212; <b>Sirnaomics Ltd. <\/b>(the <b>&#8220;Company&#8221;<\/b>, Stock Code: 2257.HK, together with its subsidiaries, the <b>&#8220;Group&#8221;<\/b> or <b>&#8220;Sirnaomics&#8221;<\/b>), a leading biopharmaceutical company in discovery and development of RNAi therapeutics, today announced the interim results of an ongoing Phase I clinical trial of STP705, an siRNA (small interfering RNA) drug candidate, for fat reduction in adults undergoing abdominoplasty. The initial results of the Phase I trial appear to indicate that the use of STP705 in the treatment of unwanted fat is safe and show clear signs of efficacy.<\/p>\n<p>This interim efficacy results examined efficacy data from six participants that were&nbsp;scheduled to undergo abdominoplasty. Each participant was treated with STP705 doses of&nbsp;120 \u03bcg, 240 \u03bcg and 320 \u03bcg at volume per injection of either 0.5 ml or 1.0 ml per injection&nbsp;site as well as placebo consisting of normal saline. The test article administration area&nbsp;was the central to lower abdomen region designated for abdominoplasty and participants&nbsp;received a single injection per site up to three injections of test article approximately 28&nbsp;days apart. Participants in the safety review were examined for the presence of and severity&nbsp;of Local Skin Reactions (LSR) including erythema, edema, and bruising over a time frame&nbsp;as well as the incidence (severity and causality) of any adverse events for a time frame of&nbsp;approximately 98 days. Secondary analysis looked at histological evidence of fat changes&nbsp;that would be seen in fat tissue remodeling such as fat inflammation, panniculitis, fibrosis&nbsp;and fat necrosis. Statistical analysis was performed with non-parametric one-way ANOVA&nbsp;using Kruskal-Wallis test and Dunn&#8217;s multiple comparison test.<\/p>\n<p>The interim analysis results include data from six participants with 42 tissue samples in total. There were no significant adverse events and all tissue samples examined in this&nbsp;review using variables doses of STP705 showed histological evidence suggestive of fat&nbsp;remodeling. Based on the histological scoring and panniculitis + fat necrosis ranking, a&nbsp;dose-dependent effect was observed for all treatment groups comparing to the placebo group&nbsp;with statistical significance (P &lt; 0.05). The 240 \u03bcg at the volume of 1.0 ml treatment group&nbsp;has demonstrated the most potent activity.<\/p>\n<p>Professor <span class=\"xn-person\">Mark Nestor<\/span>, M.D., Ph.D., Director of the Center for Clinical and Cosmetic&nbsp;Research and the Center for Cosmetic Enhancement, <span class=\"xn-location\">Aventura, Florida<\/span>, a Voluntary&nbsp;Professor in the Division of Plastic Surgery at the <span class=\"xn-org\">University of Miami<\/span>, <span class=\"xn-person\">Miller School<\/span> of&nbsp;Medicine and the principal investigator (PI) of the Phase I clinical study commented, &#8220;the&nbsp;initial data from the Phase I trial appears to indicate that the use of STP705 in the treatment&nbsp;of unwanted fat is safe and shows clear signs of efficacy. Safety has been examined in the&nbsp;first of three subjects and histology of the injected areas post abdominoplasty has been&nbsp;evaluated. Regarding histology, there is a clear difference in many of the specimens between&nbsp;the placebo, and the subjects injected with STP705. We look forward to completing this first&nbsp;study and analyzing all the results in the near future.&#8221;<\/p>\n<p>&#8220;Interim data from our clinical study of STP705 for fat reduction indicate that subjects that have received various doses of STP705 show clear histologic evidence of fat&nbsp;changes that would be observed in fat remodeling,&#8221; said Dr. <span class=\"xn-person\">Michael Molyneaux<\/span>, M.D.,&nbsp;Executive Director and Chief Medical Officer of Sirnaomics. &#8220;The safety results were very&nbsp;encouraging with no systemic adverse events and no significant local skin or tissue changes.&nbsp;This finding is very important when selecting a product that will be used for non-surgical&nbsp;fat remodeling and the fact that there was clear histological evidence of fat remodeling in a dose dependent manner is very encouraging as we move into Phase II of the program. We anticipate final study report sometime in Q3 2023 after which time, we will request a meeting with the FDA to determine the path to approval for the program.&#8221;<\/p>\n<p>This study is the Group&#8217;s first exploration to apply an RNAi therapeutic candidate for&nbsp;localized fat remodeling and Sirnaomics plans to use the information from this study to&nbsp;expand into the treatment of submental fat and other areas of noninvasive fat remodeling.&nbsp;The positive interim results have better informed the Group about the later stage&nbsp;development of STP705 in the medical aesthetics category. Together with the positive&nbsp;results from STP705 for treatment of squamous cell carcinoma in situ (isSCC) and basal cell&nbsp;carcinoma (BCC), the Group has successfully leveraged the proof-of-concept human data&nbsp;from STP705. This advancement in fat remodeling is expected to open up a new therapeutic&nbsp;area of medical aesthetics for Sirnaomics&#8217; pipeline and has received very positive responses&nbsp;from the market.<\/p>\n<p>&#8220;The interim results of this Phase I clinical study have brought a strong enthusiasm using&nbsp;RNAi drug for medical aesthetic treatment. This novel non-invasive fat-reduction option&nbsp;potentially offers millions of people with unwanted fat on their bodies, which are resistant&nbsp;to diet and exercise and influenced by aging and genetics, a unique way to address those&nbsp;all-too-common conditions,&#8221; said Dr. <span class=\"xn-person\">Patrick Lu<\/span>, Founder, Chairman of the Board,&nbsp;Executive Director, President and Chief Executive Officer of Sirnaomics. &#8220;During our&nbsp;preclinical studies with a well-defined animal model, we found that STP705 demonstrated&nbsp;superior efficacy and safety, compared to a commercially available injection drug for the&nbsp;same indication. This observation encourages us not only to explore the utility of STP705&nbsp;for medical aesthetics but also to advance it to become a best-in-class drug candidate for&nbsp;fat-remodeling.&#8221;<\/p>\n<p>Additional information about this clinical trial is available at clinicaltrials.gov using the&nbsp;identifier: NCT05422378.<\/p>\n<p><b><u>About STP705<br \/><\/u><\/b>Sirnaomics&#8217; leading product candidate, STP705, is a siRNA (small interfering RNA)&nbsp;therapeutic that takes advantage of a dual-targeted inhibitory property and polypeptide&nbsp;nanoparticle (PNP)-enhanced delivery to directly knock down both TGF-\u03b21 and COX-2&nbsp;gene expression. The product candidate has received multiple IND approvals from both&nbsp;the U.S. Food and Drug Administration (FDA) and the Chinese National Medical Products&nbsp;Administration (NMPA), including treatments of cholangiocarcinoma, non-melanoma&nbsp;skin cancer and hypertrophic scar. There are currently three product pipeline advancing&nbsp;programs prioritized by STP705: a Phase IIb for squamous cell carcinoma in situ (isSCC),&nbsp;a Phase II for basal cell carcinoma (BCC) and a Phase I for the fat remodeling. In addition,&nbsp;in the treatment of other indications, STP705 has received Orphan Drug Designation for the&nbsp;treatment of cholangiocarcinoma (CCA) and primary sclerosing cholangitis (PSC).<\/p>\n<p><b><u>About Sirnaomics Ltd. (Stock Code: 2257)<br \/><\/u><\/b>Sirnaomics is an RNA therapeutics biopharmaceutical company with product candidates in&nbsp;preclinical and clinical stages that focuses on the discovery and development of innovative&nbsp;drugs for indications with medical needs and large market opportunities. Sirnaomics is the&nbsp;first clinical-stage RNA therapeutics company to have a strong presence in both <span class=\"xn-location\">Asia<\/span> and&nbsp;the <span class=\"xn-location\">United States<\/span>. Based on its proprietary delivery technologies: Polypeptide Nanoparticle&nbsp;Formulation and the 2nd generation of GalNAc conjugation, the Group has established&nbsp;an enriched drug candidate pipeline. Sirnaomics is currently holding a leadership position&nbsp;on advancing RNAi therapeutics for oncology application with multiple successes of its&nbsp;clinical programs for STP705 and STP707. STP122G represents the first drug candidate&nbsp;of GalAhead\u2122 technology entering clinical development. With the establishment of the&nbsp;Group&#8217;s manufacturing facility, Sirnaomics currently is undergoing a transition from a&nbsp;biotech company to a biopharma corporation. Learn more at: <a href=\"http:\/\/www.sirnaomics.com\/\" target=\"_blank\" rel=\"nofollow noopener\">www.sirnaomics.com<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>HONG KONG, GERMANTOWN,&nbsp;Md. and SUZHOU,&nbsp;China, June 5, 2023 \/PRNewswire\/ &#8212; Sirnaomics Ltd. (the &#8220;Company&#8221;, Stock Code: 2257.HK, together with its subsidiaries, the &#8220;Group&#8221; or &#8220;Sirnaomics&#8221;), a leading biopharmaceutical company in discovery and development of RNAi therapeutics, today announced the interim results of an ongoing Phase I clinical trial of STP705, an siRNA (small interfering RNA) [&hellip;]<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[20],"tags":[],"class_list":["post-19200","post","type-post","status-publish","format-standard","hentry","category-business-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Sirnaomics Reports Interim Results of STP705 Phase I Clinical Study for Medical Aesthetics Treatment in Adults Undergoing Abdominoplasty - My Blog<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/transmediavictoria.net.au\/?p=19200\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sirnaomics Reports Interim Results of STP705 Phase I Clinical Study for Medical Aesthetics Treatment in Adults Undergoing Abdominoplasty - My Blog\" \/>\n<meta property=\"og:description\" content=\"HONG KONG, GERMANTOWN,&nbsp;Md. and SUZHOU,&nbsp;China, June 5, 2023 \/PRNewswire\/ &#8212; Sirnaomics Ltd. (the &#8220;Company&#8221;, Stock Code: 2257.HK, together with its subsidiaries, the &#8220;Group&#8221; or &#8220;Sirnaomics&#8221;), a leading biopharmaceutical company in discovery and development of RNAi therapeutics, today announced the interim results of an ongoing Phase I clinical trial of STP705, an siRNA (small interfering RNA) [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/transmediavictoria.net.au\/?p=19200\" \/>\n<meta property=\"og:site_name\" content=\"My Blog\" \/>\n<meta property=\"article:published_time\" content=\"2023-06-05T11:12:00+00:00\" \/>\n<meta name=\"author\" content=\"admin_tony\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"admin_tony\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"6 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/transmediavictoria.net.au\\\/?p=19200#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/transmediavictoria.net.au\\\/?p=19200\"},\"author\":{\"name\":\"admin_tony\",\"@id\":\"https:\\\/\\\/transmediavictoria.net.au\\\/#\\\/schema\\\/person\\\/5b51d407d652c0aa802bea269ea5d7e7\"},\"headline\":\"Sirnaomics Reports Interim Results of STP705 Phase I Clinical Study for Medical Aesthetics Treatment in Adults Undergoing Abdominoplasty\",\"datePublished\":\"2023-06-05T11:12:00+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/transmediavictoria.net.au\\\/?p=19200\"},\"wordCount\":1282,\"articleSection\":[\"Business News\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/transmediavictoria.net.au\\\/?p=19200\",\"url\":\"https:\\\/\\\/transmediavictoria.net.au\\\/?p=19200\",\"name\":\"Sirnaomics Reports Interim Results of STP705 Phase I Clinical Study for Medical Aesthetics Treatment in Adults Undergoing Abdominoplasty - 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