{"id":406371,"date":"2020-12-29T17:18:18","date_gmt":"2020-12-29T22:18:18","guid":{"rendered":"http:\/\/www.marketnewsdesk.com\/?p=406371"},"modified":"2020-12-29T17:18:18","modified_gmt":"2020-12-29T22:18:18","slug":"osmotica-pharmaceuticals-plc-receives-complete-response-letter-from-u-s-food-and-drug-administration-for-arbaclofen-extended-release-tablets","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/osmotica-pharmaceuticals-plc-receives-complete-response-letter-from-u-s-food-and-drug-administration-for-arbaclofen-extended-release-tablets\/","title":{"rendered":"Osmotica Pharmaceuticals plc Receives Complete Response Letter from U.S. Food and Drug Administration for Arbaclofen Extended Release Tablets"},"content":{"rendered":"
\n

BRIDGEWATER, N.J., Dec. 29, 2020 (GLOBE NEWSWIRE) — Osmotica Pharmaceuticals plc (Nasdaq: OSMT) (\u201cOsmotica\u201d or the \u201cCompany\u201d) today announced that the U.S. Food and Drug Administration (\u201cFDA\u201d) has issued a Complete Response Letter (\u201cCRL\u201d) regarding the Company’s New Drug Application (\u201cNDA\u201d) seeking approval for the investigational agent arbaclofen extended release (“ER”) tablets to treat spasticity resulting from multiple sclerosis.<\/p>\n

The CRL stated that the Company did not provide adequate justification (including in its most recent NDA amendment) for the statistical analysis of the change from baseline to Day 84 in TNmAS-MAL scores comparing arbaclofen 40 mg to placebo, one of the co-primary endpoints. The FDA made a number of recommendations in its CRL, including that the Company conduct a new study in order to provide substantial evidence of efficacy of arbaclofen.<\/p>\n

“We believe we have provided data supporting the efficacy and safety for both the 40 mg\/day and 80 mg\/day doses of arbaclofen. There is a tremendous unmet need for better treatments to help MS patients cope with spasticity, and we believe our safety and efficacy database for both strengths of arbaclofen provides a meaningful body of evidence that should support approval,\u201d said Brian Markison, CEO of Osmotica.<\/p>\n

The Company intends to review the CRL with its advisors and to request a meeting with the FDA to discuss their recommendations.<\/p>\n

\n About Arbaclofen ER<\/strong>\n <\/p>\n

Osmotica Pharmaceutical plc is developing arbaclofen (the active R-enantiomer of baclofen) ER tablets for the treatment of spasticity in patients with MS. This program aims to demonstrate the clinical efficacy and safety of arbaclofen ER tablets in patients with spasticity due to MS.<\/p>\n

\n About\u00a0Osmotica Pharmaceuticals plc<\/strong>\n <\/p>\n

Osmotica Pharmaceuticals plc\u00a0is a fully integrated biopharmaceutical company focused on the development and commercialization of specialty products that target markets with underserved patient populations. RVL Pharmaceuticals, Inc.\u00a0is the Company\u2019s ophthalmic subsidiary supporting UPNEEQ.\u00a0Vertical Pharmaceuticals, LLC\u00a0represents the Company\u2019s diversified branded portfolio and\u00a0Trigen Laboratories, LLC\u00a0represents the Company\u2019s non-promoted products, including complex generic formulations.<\/p>\n

\n Forward Looking Statements<\/strong>\n <\/p>\n

This press release includes statements that express the Company\u2019s opinions, expectations, beliefs, plans, objectives, assumptions or projections regarding future events or future results and therefore are, or may be deemed to be, \u201cforward-looking statements.\u201d The Company\u2019s actual results may vary significantly from the results anticipated in these forward-looking statements, which can generally be identified by the use of forward-looking terminology, including the terms \u201cbelieves,\u201d \u201cexpects,\u201d \u201cmay,\u201d \u201cwill,\u201d \u201cshould,\u201d \u201cseeks,\u201d \u201cprojects,\u201d \u201capproximately,\u201d \u201cintends,\u201d \u201cplans,\u201d \u201cestimates\u201d or \u201canticipates,\u201d or, in each case, their negatives or other variations or comparable terminology. These forward-looking statements include all matters that are not historical facts. They include statements regarding the Company\u2019s intentions, beliefs or current expectations concerning, among other things, our results of operations, financial condition, liquidity, prospects, financial guidance, growth plan, strategies, trends and other events, particularly relating to sales of current products and the development, approval and introduction of new products, FDA and other regulatory applications, approvals and actions, the continuation of historical trends, and the sufficiency of our cash balances and cash generated from operating and financing activities for future liquidity and capital resource needs. By their nature, forward-looking statements involve risks and uncertainties because they relate to events and depend on circumstances that may or may not occur in the future. We may not achieve the plans, intentions or expectations disclosed in our forward-looking statements, and you should not place significant reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements we make. Important factors that could cause actual results and events to differ materially from those indicated in the forward-looking statements include the following: our business may be adversely affected by the ongoing coronavirus outbreak; our ability to successfully develop or commercialize new products, or do so on a timely or cost effective basis; our dependence on a limited number of products; failures of or delays in clinical trials or other delays in obtaining regulatory approval or commencing product sales for new products; the impact of legal proceedings; our ability to service our substantial debt; our ability to raise additional capital; the impact of competition from both brand and generic companies; any interruption at our manufacturing facility, our warehouses or at facilities operated by third parties that we rely on for our products; our dependence on our major customers; our ability to develop and maintain our sales capabilities; any changes to the coverage and reimbursement levels for our products by governmental authorities and other third-party payors as a result of healthcare reform or otherwise; the impact of any changes in the extensive governmental regulation that we face; manufacturing or quality control issues that we may face; and other risks and uncertainties more fully described in the \u201cRisk Factors\u201d section of our Annual Report on Form 10-K for the year ended December 31, 2019, our Quarterly Reports on Form 10-Q for the quarterly periods ended March 31, 2020, June 30, 2020\u00a0and September 30, 2020 and other filings that the Company makes with the Securities and Exchange Commission. These forward-looking statements speak only as of the time of this release and we do not undertake to publicly update or revise them, whether as a result of new information, future events or otherwise, except as required by law.<\/p>\n

\n Investor and Media Relations for Osmotica Pharmaceuticals plc<\/strong>
\n
Lisa M. Wilson
In-Site Communications, Inc.
T: 212-452-2793
E: lwilson@insitecony.com<\/u><\/a>\u00a0<\/p>\n

\u00a0<\/p>\n


\n
\n \n <\/div>\n

<\/div>\n","protected":false},"excerpt":{"rendered":"

BRIDGEWATER, N.J., Dec. 29, 2020 (GLOBE NEWSWIRE) — Osmotica Pharmaceuticals plc (Nasdaq: OSMT) (\u201cOsmotica\u201d or the \u201cCompany\u201d) today announced that the U.S. Food and Drug Administration (\u201cFDA\u201d) has issued a Complete Response Letter (\u201cCRL\u201d) regarding the Company’s New Drug Application (\u201cNDA\u201d) seeking approval for the investigational agent arbaclofen extended release (“ER”) tablets to treat spasticity resulting from multiple sclerosis. The CRL stated that the Company did not provide adequate justification (including in its most recent NDA amendment) for the statistical analysis of the change from baseline to Day 84 in TNmAS-MAL scores comparing arbaclofen 40 mg to placebo, one of the co-primary endpoints. The FDA made a number of recommendations in its CRL, including that the Company conduct a new … <\/p>\n

Continue reading “Osmotica Pharmaceuticals plc Receives Complete Response Letter from U.S. Food and Drug Administration for Arbaclofen Extended Release Tablets”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-406371","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nOsmotica Pharmaceuticals plc Receives Complete Response Letter from U.S. Food and Drug Administration for Arbaclofen Extended Release Tablets - Market Newsdesk<\/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:\/\/www.marketnewsdesk.com\/index.php\/osmotica-pharmaceuticals-plc-receives-complete-response-letter-from-u-s-food-and-drug-administration-for-arbaclofen-extended-release-tablets\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Osmotica Pharmaceuticals plc Receives Complete Response Letter from U.S. Food and Drug Administration for Arbaclofen Extended Release Tablets - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"BRIDGEWATER, N.J., Dec. 29, 2020 (GLOBE NEWSWIRE) — Osmotica Pharmaceuticals plc (Nasdaq: OSMT) (\u201cOsmotica\u201d or the \u201cCompany\u201d) today announced that the U.S. Food and Drug Administration (\u201cFDA\u201d) has issued a Complete Response Letter (\u201cCRL\u201d) regarding the Company’s New Drug Application (\u201cNDA\u201d) seeking approval for the investigational agent arbaclofen extended release (“ER”) tablets to treat spasticity resulting from multiple sclerosis. 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The CRL stated that the Company did not provide adequate justification (including in its most recent NDA amendment) for the statistical analysis of the change from baseline to Day 84 in TNmAS-MAL scores comparing arbaclofen 40 mg to placebo, one of the co-primary endpoints. 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