{"id":49975,"date":"2022-10-24T13:01:58","date_gmt":"2022-10-24T11:01:58","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/novaliq-announces-fda-acceptance-of-the-new-drug-application-for-cyclasol-for-the-treatment-of-dry-eye-disease\/"},"modified":"2022-10-24T13:01:58","modified_gmt":"2022-10-24T11:01:58","slug":"novaliq-announces-fda-acceptance-of-the-new-drug-application-for-cyclasol-for-the-treatment-of-dry-eye-disease","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/novaliq-announces-fda-acceptance-of-the-new-drug-application-for-cyclasol-for-the-treatment-of-dry-eye-disease\/","title":{"rendered":"Novaliq Announces FDA Acceptance of the New Drug Application for CyclASol\u00ae for the Treatment of Dry Eye Disease"},"content":{"rendered":"<div>\n<ul class=\"bwlistdisc\">\n<li>\nPDUFA target action date is June 8, 2023\n<\/li>\n<\/ul>\n<p>HEIDELBERG, Germany, and CAMBRIDGE, MA, USA&#8211;(BUSINESS WIRE)&#8211;<a href=\"https:\/\/twitter.com\/hashtag\/cyclasol?src=hash\" target=\"_blank\" rel=\"noopener\">#cyclasol<\/a>&#8211;Novaliq, a biopharmaceutical company focusing on first- and best-in-class ocular therapeutics based on the unique EyeSol<sup>\u00ae<\/sup> water-free technology, today announced that the U.S. Food and Drug Administration (FDA) has accepted the New Drug Application (NDA) for CyclASol<sup>\u00ae<\/sup> (cyclosporine ophthalmic solution), a first-of-its-kind anti-inflammatory product for the treatment for the signs and symptoms of dry eye disease (DED).\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20221024005092\/en\/1610006\/5\/Novaliq_Logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20221024005092\/en\/1610006\/21\/Novaliq_Logo.jpg\"><\/a><\/p>\n<p>\nThe Agency completed the filing review of the CyclASol<sup>\u00ae<\/sup> NDA and determined that the application is sufficiently complete to permit a substantive review. No potential review issues have been identified at this time. The Prescription Drug User Fee Act (PDUFA) target action date set by the FDA for announcing its decision on Novaliq\u2019s NDA after reviewing the application is June 8, 2023.\n<\/p>\n<p>\n\u201cThis is an exciting time for ophthalmologists and optometrists and their patients as we are one step closer to address important needs and to better treat a serious ocular surface condition affecting millions of Americans\u201d, said Christian Roesky, Ph.D., CEO, Novaliq. \u201cIf approved, CyclASol<sup>\u00ae<\/sup> would be a highly potent but comfortable anti-inflammatory therapy for patients with dry eye disease. It shows impressive and rapid therapeutic effects objectively measured on the ocular surface in the majority of patients, with clinical benefits on the signs and symptoms of the disease.\u201d\n<\/p>\n<p>\nCyclASol<sup>\u00ae<\/sup> has demonstrated in two pivotal studies fast onset of therapeutic effect in afflicted patients in this indication, clinical meaningful improvement of ocular surface damage, and excellent tolerability. Results from a 12-month long-term study confirmed that the effects are maintained, and even improved for most sign and symptom endpoints.\n<\/p>\n<p>\n\u201cThis important milestone marks the second NDA acceptance of water-free dry eye therapies in less than 3 months.<sup>1<\/sup> The two distinct modalities of action of the EyeSol<sup>\u00ae<\/sup>-based dry eye therapies open new and complimentary clinical prospects on how to treat DED in the future,\u201d said Sonja Kr\u00f6sser, Ph.D., Vice President Preclinical &amp; Clinical Development at Novaliq. \u201cWe are committed to work closely with the FDA to bring this novel cyclosporine drug product to patients suffering from DED as quickly as possible.\u201d\n<\/p>\n<p>\nDry eye is one of the most common ocular surface disorders, with approximately 18 million Americans diagnosed with DED.<sup>2,3<\/sup> Inflammation and immunologic processes play a key role in the pathology of the disease.\n<\/p>\n<p>\nNovaliq further plans to submit a marketing authorization application to the European Medicines Agency and further authorities in 2023.\n<\/p>\n<p>\n<b>About Novaliq<br \/>\n<br \/><\/b>Novaliq is a biopharmaceutical company focusing on the development and commercialization of first- and best-in-class ocular therapeutics based on EyeSol<sup>\u00ae<\/sup>, the worldwide first water-free technology.\n<\/p>\n<p>\nEyeSol<sup>\u00ae<\/sup> is Novaliq\u2019s proprietary water-free technology using ultrapure semifluorinated alkanes (SFAs) that are physically, chemically, and physiologically inert with excellent biocompatibility and a very good safety profile. Novaliq offers an industry-leading portfolio addressing today\u2019s unmet medical needs of millions of patients with eye diseases.\n<\/p>\n<p>\nIn September 2022 acceptance of filing of a New Drug Application (NDA) by the U.S. Food and Drug Administration (FDA) was announced for NOV03 (perfluorohexyloctane), for the proposed indication of treating the signs and symptoms of dry eye disease (DED) associated with Meibomian gland dysfunction (MGD). PDUFA target action date for NOV03 is June 28, 2023. In addition to CyclASol<sup>\u00ae<\/sup>, the company continues to progress multiple additional pipeline opportunities based on its validated EyeSol<sup>\u00ae<\/sup> platform, both in ophthalmology and adjacent indications like dermatology.\n<\/p>\n<p>\nNovaliq GmbH is headquartered in Heidelberg, Germany and Novaliq Inc. has an office in Cambridge, MA, USA. The long-term shareholder is dievini Hopp BioTech holding GmbH &amp; Co. KG, an active investor in Life and Health Sciences companies. More on <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=http%3A%2F%2Fwww.novaliq.com&amp;esheet=52949920&amp;newsitemid=20221024005092&amp;lan=en-US&amp;anchor=www.novaliq.com&amp;index=1&amp;md5=9f82161f8af936efaec2568cb6c510b8\" rel=\"nofollow noopener\" shape=\"rect\">www.novaliq.com<\/a>.\n<\/p>\n<p>\n<b>Recommended Readings<\/b>\n<\/p>\n<ol class=\"bwlistdecimal\">\n<li>\n<a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.novaliq.com%2Fpress-releases%2F2022%2F09%2F07%2Ffda-accepts-nda-filing-for-nov03%2F&amp;esheet=52949920&amp;newsitemid=20221024005092&amp;lan=en-US&amp;anchor=https%3A%2F%2Fwww.novaliq.com%2Fpress-releases%2F2022%2F09%2F07%2Ffda-accepts-nda-filing-for-nov03%2F&amp;index=2&amp;md5=13e255797dff5942c15af3340d87f231\" rel=\"nofollow noopener\" shape=\"rect\">https:\/\/www.novaliq.com\/press-releases\/2022\/09\/07\/fda-accepts-nda-filing-for-nov03\/<\/a>\n<\/li>\n<li>\nLeonardi A, Modugno RL, &amp; Salami E. Allergy and Dry Eye Disease. Ocular immunology and inflammation. 2021; 29:1168\u20131176\n<\/li>\n<li>\n2020 Dry Eye Products Market Report: A global Analysis for 2019 to 2025. Market Scope\n<\/li>\n<\/ol>\n<p>\n<i>Any product\/brand names and\/or logos are trademarks of the respective owners.<br \/>\n<br \/><\/i><i>\u00a9 2022 Novaliq GmbH, Heidelberg, Germany.<\/i>\n<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\n<b>Novaliq Media Contact:<\/b><br \/>Simone Angstmann-Mehr<br \/>\n<br \/><a target=\"_blank\" href=\"&#109;&#97;&#x69;l&#116;&#x6f;&#x3a;i&#110;&#x66;&#x6f;&#64;&#110;&#x6f;&#x76;a&#108;&#x69;&#x71;&#46;&#99;&#x6f;&#x6d;\" rel=\"nofollow noopener\" shape=\"rect\">&#x69;&#x6e;&#x66;&#x6f;&#x40;&#x6e;&#x6f;&#x76;&#x61;&#x6c;&#x69;&#x71;&#x2e;&#x63;&#x6f;&#x6d;<\/a>\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>PDUFA target action date is June 8, 2023 HEIDELBERG, Germany, and CAMBRIDGE, MA, USA&#8211;(BUSINESS WIRE)&#8211;#cyclasol&#8211;Novaliq, a biopharmaceutical company focusing on first- and best-in-class ocular therapeutics based on the unique EyeSol\u00ae water-free technology, today announced that the U.S. Food and Drug Administration (FDA) has accepted the New Drug Application (NDA) for CyclASol\u00ae (cyclosporine ophthalmic solution), a &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/novaliq-announces-fda-acceptance-of-the-new-drug-application-for-cyclasol-for-the-treatment-of-dry-eye-disease\/\">[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-49975","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>Novaliq Announces FDA Acceptance of the New Drug Application for CyclASol\u00ae for the Treatment of Dry Eye Disease - 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\/novaliq-announces-fda-acceptance-of-the-new-drug-application-for-cyclasol-for-the-treatment-of-dry-eye-disease\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Novaliq Announces FDA Acceptance of the New Drug Application for CyclASol\u00ae for the Treatment of Dry Eye Disease - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"PDUFA target action date is June 8, 2023 HEIDELBERG, Germany, and CAMBRIDGE, MA, USA&#8211;(BUSINESS WIRE)&#8211;#cyclasol&#8211;Novaliq, a biopharmaceutical company focusing on first- and best-in-class ocular therapeutics based on the unique EyeSol\u00ae water-free technology, today announced that the U.S. Food and Drug Administration (FDA) has accepted the New Drug Application (NDA) for CyclASol\u00ae (cyclosporine ophthalmic solution), a ... 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