{"id":55028,"date":"2023-03-21T13:07:23","date_gmt":"2023-03-21T12:07:23","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/lumicell-submits-new-drug-application-for-lumisight-optical-imaging-agent-to-u-s-fda-for-intraoperative-breast-cancer-detection-and-removal\/"},"modified":"2023-03-21T13:07:23","modified_gmt":"2023-03-21T12:07:23","slug":"lumicell-submits-new-drug-application-for-lumisight-optical-imaging-agent-to-u-s-fda-for-intraoperative-breast-cancer-detection-and-removal","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/lumicell-submits-new-drug-application-for-lumisight-optical-imaging-agent-to-u-s-fda-for-intraoperative-breast-cancer-detection-and-removal\/","title":{"rendered":"Lumicell Submits New Drug Application for LUMISIGHT\u2122 Optical Imaging Agent to U.S. FDA for Intraoperative Breast Cancer Detection and Removal"},"content":{"rendered":"<div>\n<ul class=\"bwlistdisc\">\n<li>\n<i>Novel optical imaging agent highlights cancerous tissue during initial lumpectomy to enable a more complete resection as part of the investigational Lumicell Direct Visualization System<\/i>\n<\/li>\n<li>\n<i>LUMISIGHT was previously granted Fast Track designation by the FDA<\/i>\n<\/li>\n<li>\n<i>Pan-oncological optical imaging agent also being studied for other solid tumors<\/i>\n<\/li>\n<\/ul>\n<p>NEWTON, Mass.&#8211;(BUSINESS WIRE)&#8211;<a href=\"https:\/\/twitter.com\/hashtag\/BreakthroughDevice?src=hash\" target=\"_blank\" rel=\"noopener\">#BreakthroughDevice<\/a>&#8212;<a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=http%3A%2F%2Flumicell.com%2Findex.html&amp;esheet=53356067&amp;newsitemid=20230303005315&amp;lan=en-US&amp;anchor=Lumicell%2C+Inc&amp;index=1&amp;md5=5480cfef8826bdf144744b22351e01c7\" rel=\"nofollow noopener\" shape=\"rect\">Lumicell, Inc<\/a>., a privately held company focused on innovative fluorescence-guided imaging technologies for cancer surgery, today announced a New Drug Application (NDA) for its LUMISIGHT\u2122 Optical Imaging Agent has been submitted to the U.S. Food and Drug Administration (FDA).\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20230303005315\/en\/1729514\/5\/probe_lay_down_family_vial_w_syringe_no_needle.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20230303005315\/en\/1729514\/21\/probe_lay_down_family_vial_w_syringe_no_needle.jpg\"><\/a><br \/><a href=\"https:\/\/mms.businesswire.com\/media\/20230303005315\/en\/1729503\/5\/Lumicell_Logo-SSO.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20230303005315\/en\/1729503\/21\/Lumicell_Logo-SSO.jpg\"><\/a><\/p>\n<p>\nLUMISIGHT is intended for use with the Lumicell\u2122 Direct Visualization System (DVS), an investigational system designed to assist in the detection of residual cancerous tissue within the lumpectomy cavity following removal of the primary specimen during breast conserving surgery.\n<\/p>\n<p>\n\u201cLumicell is committed to revolutionizing the way breast cancer surgery is performed and bringing the benefits of the Lumicell Direct Visualization System to breast cancer patients,\u201d said Kevin Hershberger, president and chief executive officer of Lumicell. \u201cSubmission of the LUMISIGHT NDA is a significant step toward achieving this goal. We look forward to working with the FDA on acceptance of our LUMISIGHT application for review and submitting the PMA for the Lumicell DVS in the second quarter.\u201d\n<\/p>\n<p>\nThe LUMISIGHT NDA submission is supported by data from more than 700 breast cancer patients across five clinical studies at top academic and regional community cancer centers. Results from the Investigation of Novel Surgical Imaging for Tumor Excision (INSITE) pivotal trial (<a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fct2%2Fshow%2FNCT03686215&amp;esheet=53356067&amp;newsitemid=20230303005315&amp;lan=en-US&amp;anchor=NCT03686215&amp;index=2&amp;md5=e47d146e2f44b499fd2818375d2ffeb5\" rel=\"nofollow noopener\" shape=\"rect\">NCT03686215<\/a>) of 406 patients at 14 sites will be presented at the upcoming American Society of Breast Surgeons (ASBrS) annual meeting. The FDA granted LUMISIGHT Fast Track designation and the Lumicell DVS Breakthrough Device designation in recognition of its potential benefit of identifying residual cancer after the initial lumpectomy.\n<\/p>\n<p>\n\u201cData has shown that the risk of local recurrence is directly related to incomplete tumor removal. Currently, at least 20% of women having breast conserving surgery require a second surgery because of positive margins and 6-10% of women with breast cancer experience a local recurrence,\u201d said Barbara Smith, MD, PhD, director of the Breast Program at Massachusetts General Hospital, professor of surgery at Harvard Medical School and lead investigator of the INSITE clinical trial. \u201cAs surgeons, technology that helps ensure we are doing everything in our power to remove cancer during the initial lumpectomy gives us and patients greater piece of mind and has the potential to support improved outcomes.\u201d\n<\/p>\n<p>\n<b>About the Lumicell Direct Visualization System<\/b>\n<\/p>\n<p>\nThe investigational Lumicell Direct Visualization System (DVS) is intended for use with the LUMISIGHT Optical Imaging Agent and features a hand-held imaging probe that is designed to go inside the breast cavity and a patient-calibrated cancer detection software to assist in the detection of residual cancer, thereby enabling a more complete resection. The safety and efficacy of the Lumicell DVS in detecting residual cancer left behind by standard of care surgical procedures has been evaluated in two studies: INSITE and a feasibility study of 234 patients at 16 sites, results of which were published in <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fjamanetwork.com%2Fjournals%2Fjamasurgery%2Ffullarticle%2F2792167&amp;esheet=53356067&amp;newsitemid=20230303005315&amp;lan=en-US&amp;anchor=JAMA+Surgery&amp;index=3&amp;md5=b2dba9e9bef7afca1bc9b93c577c66c7\" rel=\"nofollow noopener\" shape=\"rect\">JAMA Surgery<\/a>.\n<\/p>\n<p>\nThe Lumicell DVS and LUMISIGHT are limited by Federal (or United States) law to investigational use only. The Lumicell DVS is not commercially available.\n<\/p>\n<p>\n<b>About Lumicell, Inc.<\/b>\n<\/p>\n<p>\nLumicell is a privately held company focused on improving surgical outcomes and reducing healthcare costs by utilizing its innovative fluorescence-guided surgical technologies to enable a more complete resection of cancer that may have otherwise been left behind. The company\u2019s first product in development is the Lumicell Direct Visualization System, designed to illuminate cancerous tissue within the breast cavity during the initial lumpectomy procedure. Lumicell\u2019s proprietary, pan-oncologic optical imaging agent LUMISIGHT is also being explored across a wide variety of solid tumor indications. For more information, please visit <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=http%3A%2F%2Fwww.lumicell.com%2F&amp;esheet=53356067&amp;newsitemid=20230303005315&amp;lan=en-US&amp;anchor=www.lumicell.com&amp;index=4&amp;md5=68ce61f93c81d33dab8df381d187c26b\" rel=\"nofollow noopener\" shape=\"rect\">www.lumicell.com<\/a> and follow the company on <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.facebook.com%2FLumicellSurg&amp;esheet=53356067&amp;newsitemid=20230303005315&amp;lan=en-US&amp;anchor=Facebook&amp;index=5&amp;md5=efa872c63758f8e1cb3ff33146cfcc30\" rel=\"nofollow noopener\" shape=\"rect\">Facebook<\/a>, <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Ftwitter.com%2FLumicellSurg&amp;esheet=53356067&amp;newsitemid=20230303005315&amp;lan=en-US&amp;anchor=Twitter&amp;index=6&amp;md5=9772d2f5eae51301c40c7ab720f2daba\" rel=\"nofollow noopener\" shape=\"rect\">Twitter<\/a> and <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F1941596&amp;esheet=53356067&amp;newsitemid=20230303005315&amp;lan=en-US&amp;anchor=LinkedIn&amp;index=7&amp;md5=471190cb0f0e7a8786cea53b2c1c001c\" rel=\"nofollow noopener\" shape=\"rect\">LinkedIn<\/a>.\n<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\nJoni Ramirez<br \/>\n<br \/>Merryman Communications<br \/>\n<br \/><a target=\"_blank\" href=\"&#x6d;&#97;&#x69;&#x6c;&#116;&#x6f;&#58;j&#x6f;&#110;i&#x40;&#109;e&#x72;&#114;y&#x6d;&#97;&#x6e;&#x63;&#111;&#x6d;&#x6d;&#117;&#x6e;&#105;c&#x61;&#116;i&#x6f;&#110;s&#x2e;&#99;o&#x6d;\" rel=\"nofollow noopener\" shape=\"rect\">jon&#105;&#64;&#109;&#x65;&#x72;&#x72;&#x79;&#x6d;&#x61;nco&#109;&#109;&#117;&#110;&#x69;&#x63;&#x61;&#x74;&#x69;&#x6f;ns&#46;&#99;&#111;&#109;<\/a><br \/>323-532-0746\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Novel optical imaging agent highlights cancerous tissue during initial lumpectomy to enable a more complete resection as part of the investigational Lumicell Direct Visualization System LUMISIGHT was previously granted Fast Track designation by the FDA Pan-oncological optical imaging agent also being studied for other solid tumors NEWTON, Mass.&#8211;(BUSINESS WIRE)&#8211;#BreakthroughDevice&#8212;Lumicell, Inc., a privately held company focused &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/lumicell-submits-new-drug-application-for-lumisight-optical-imaging-agent-to-u-s-fda-for-intraoperative-breast-cancer-detection-and-removal\/\">[Read more&#8230;]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-55028","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Lumicell Submits New Drug Application for LUMISIGHT\u2122 Optical Imaging Agent to U.S. FDA for Intraoperative Breast Cancer Detection and Removal - Pharma Trend<\/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:\/\/pharma-trend.com\/en\/lumicell-submits-new-drug-application-for-lumisight-optical-imaging-agent-to-u-s-fda-for-intraoperative-breast-cancer-detection-and-removal\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Lumicell Submits New Drug Application for LUMISIGHT\u2122 Optical Imaging Agent to U.S. FDA for Intraoperative Breast Cancer Detection and Removal - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"Novel optical imaging agent highlights cancerous tissue during initial lumpectomy to enable a more complete resection as part of the investigational Lumicell Direct Visualization System LUMISIGHT was previously granted Fast Track designation by the FDA Pan-oncological optical imaging agent also being studied for other solid tumors NEWTON, Mass.&#8211;(BUSINESS WIRE)&#8211;#BreakthroughDevice&#8212;Lumicell, Inc., a privately held company focused ... 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