{"id":494070,"date":"2021-05-17T08:03:46","date_gmt":"2021-05-17T12:03:46","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/lifecore-to-manufacture-new-innovative-drug-for-treatment-of-postoperative-pain-following-customers-fda-approval\/"},"modified":"2021-05-17T08:03:46","modified_gmt":"2021-05-17T12:03:46","slug":"lifecore-to-manufacture-new-innovative-drug-for-treatment-of-postoperative-pain-following-customers-fda-approval","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/lifecore-to-manufacture-new-innovative-drug-for-treatment-of-postoperative-pain-following-customers-fda-approval\/","title":{"rendered":"Lifecore to Manufacture New Innovative Drug for Treatment of Postoperative Pain Following Customer\u2019s FDA Approval"},"content":{"rendered":"

\nLifecore Expands its Aseptic Production of Pharmaceutical Drugs
\n<\/h2>\n
\n

CHASKA, Minn., May 17, 2021 (GLOBE NEWSWIRE) — Lifecore Biomedical, Inc., a fully-owned subsidiary of Landec Corporation\u00a0(Nasdaq: LNDC), today announced the receipt by Heron Therapeutics (\u201cHeron\u201d), one of Lifecore\u2019s customers, of U.S. Food and Drug Administration (FDA) approval for its ZYNRELEF\u2122 (formerly known as HTX-011) candidate on May 13, 2021, for which for Lifecore provides CDMO support.<\/p>\n

Heron received FDA approval for ZYNRELEF (bupivacaine and meloxicam) extended-release solution for use in adults for soft tissue or periarticular instillation to produce postsurgical analgesia for up to 72 hours after bunionectomy, open inguinal herniorrhaphy and total knee arthroplasty.\u00a0ZYNRELEF, the first and only extended-release dual-acting local anesthetic (DALA), delivers a fixed-dose combination of the local anesthetic bupivacaine and a low dose of the nonsteroidal anti-inflammatory drug (NSAID) meloxicam. The synergy between bupivacaine and meloxicam in ZYNRELEF has resulted in patients experiencing less pain, including severe pain, and fewer patients requiring opioids (opioid-free) after surgery as compared to bupivacaine solution, the current standard-of-care.<\/p>\n

Dr. Albert Bolles, Landec\u2019s Chief Executive Officer, commented, \u201cWe congratulate Heron on their approval and are proud of Lifecore\u2019s efforts in supporting the development of this innovative new opioid-free drug for overcoming postoperative pain. This is an excellent example of how Lifecore\u2019s unique capabilities can help advance product commercialization for innovative drug therapies that improve patient lives.\u201d<\/p>\n

Jim Hall, President of Lifecore, continued, \u201cWe are excited about this approval and congratulate the Heron team on achieving this major regulatory milestone. The commercial scale manufacturing process of\u00a0ZYNRELEF was successfully developed and validated at Lifecore and provides another example of Lifecore\u2019s quality systems and manufacturing engineering excellence that we provide to our partners. We greatly appreciate Heron\u2019s long-standing partnership and are pleased to be part of their ongoing commercial success.\u201d<\/p>\n

The approval of\u00a0ZYNRELEF adds to Lifecore\u2019s growing portfolio of partnerships and products, and further demonstrates Lifecore\u2019s capabilities to support the development services and manufacturing of products that must comply with the stringent clinical and regulatory standards in the pharmaceutical marketplace. Lifecore is focused on continuing to work with its partners to develop, formulate and fill pharmaceutical drugs, medical devices and combination products.<\/p>\n

\n About\u00a0Landec Corporation (Lifecore Biomedical)<\/strong>\n <\/p>\n

Landec Corporation\u00a0(Nasdaq: LNDC) is a leading innovator of diversified health and wellness solutions with two operating businesses:\u00a0Lifecore Biomedical, Inc.\u00a0and Curation Foods, Inc.\u00a0 Landec\u00a0designs, develops, manufactures and sells products for the food and biopharmaceutical industry.\u00a0Lifecore Biomedical is a fully integrated contract development and manufacturing organization (CDMO) that offers highly differentiated capabilities in the development, fill and finish of sterile injectable pharmaceutical products in syringes and vials. As a leading manufacturer of premium, injectable grade Hyaluronic Acid, Lifecore brings 35 years of expertise as a partner for global and emerging biopharmaceutical and biotechnology companies across multiple therapeutic categories to bring their innovations to market. Curation Foods\u00a0is focused on innovating and distributing plant-based foods with 100% clean ingredients to retail, club and foodservice channels throughout\u00a0North America.\u00a0Curation Foods\u00a0is able to maximize product freshness through its geographically dispersed family of growers, refrigerated supply chain and patented BreatheWay\u00ae\u00a0packaging technology. Curation Foods brands include Eat Smart\u00ae\u00a0fresh packaged vegetables and salads,\u00a0O\u00a0Olive Oil & Vinegar\u00ae premium artisan products and Yucatan\u00ae\u00a0and Cabo Fresh\u00ae avocado products. For more information about the Company, visit Landec\u2019s website at\u00a0www.landec.com<\/a>.<\/p>\n

\n Important Cautions Regarding Forward-Looking Statements<\/strong>\n <\/p>\n

This press release contains forward-looking statements regarding future events and our future results that are subject to the safe harbor created under the Private Securities Litigation Reform Act of 1995 and other safe harbors under the Securities Act of 1933 and the Securities Exchange Act of 1934. Words such as \u201canticipate\u201d, \u201cestimate\u201d, \u201cexpect\u201d, \u201cproject\u201d, \u201cplan\u201d, \u201cintend\u201d, \u201cbelieve\u201d, \u201cmay\u201d, \u201cmight\u201d, \u201cwill\u201d, \u201cshould\u201d, \u201ccan have\u201d, \u201clikely\u201d and similar expressions are used to identify forward-looking statements. All forward-looking statements involve certain risks and uncertainties that could cause actual results to differ materially, including such factors among others, as the timing and expenses associated with operations, the ability to achieve acceptance of the Company\u2019s new products in the market place. For additional information about factors that could cause actual results to differ materially from those described in the forward-looking statements, please refer to our filings with the Securities and Exchange Commission, including the risk factors contained in our most recent Quarterly Report on Form 10-Q and Annual Report on Form 10-K. Forward-looking statements represent management\u2019s current expectations and are inherently uncertain. Except as required by law, we do not undertake any obligation to update forward-looking statements made by us to reflect subsequent events or circumstances.<\/p>\n

\n Contact Information:<\/strong>
\n
Investor Relations
Jeff Sonnek
(646) 277-1263
jeff.sonnek@icrinc.com<\/p>\n


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

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

Lifecore Expands its Aseptic Production of Pharmaceutical Drugs CHASKA, Minn., May 17, 2021 (GLOBE NEWSWIRE) — Lifecore Biomedical, Inc., a fully-owned subsidiary of Landec Corporation\u00a0(Nasdaq: LNDC), today announced the receipt by Heron Therapeutics (\u201cHeron\u201d), one of Lifecore\u2019s customers, of U.S. Food and Drug Administration (FDA) approval for its ZYNRELEF\u2122 (formerly known as HTX-011) candidate on May 13, 2021, for which for Lifecore provides CDMO support. Heron received FDA approval for ZYNRELEF (bupivacaine and meloxicam) extended-release solution for use in adults for soft tissue or periarticular instillation to produce postsurgical analgesia for up to 72 hours after bunionectomy, open inguinal herniorrhaphy and total knee arthroplasty.\u00a0ZYNRELEF, the first and only extended-release dual-acting local anesthetic (DALA), delivers a fixed-dose combination of the local … <\/p>\n

Continue reading “Lifecore to Manufacture New Innovative Drug for Treatment of Postoperative Pain Following Customer\u2019s FDA Approval”<\/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-494070","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nLifecore to Manufacture New Innovative Drug for Treatment of Postoperative Pain Following Customer\u2019s FDA Approval - 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\/lifecore-to-manufacture-new-innovative-drug-for-treatment-of-postoperative-pain-following-customers-fda-approval\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Lifecore to Manufacture New Innovative Drug for Treatment of Postoperative Pain Following Customer\u2019s FDA Approval - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Lifecore Expands its Aseptic Production of Pharmaceutical Drugs CHASKA, Minn., May 17, 2021 (GLOBE NEWSWIRE) — Lifecore Biomedical, Inc., a fully-owned subsidiary of Landec Corporation\u00a0(Nasdaq: LNDC), today announced the receipt by Heron Therapeutics (\u201cHeron\u201d), one of Lifecore\u2019s customers, of U.S. Food and Drug Administration (FDA) approval for its ZYNRELEF\u2122 (formerly known as HTX-011) candidate on May 13, 2021, for which for Lifecore provides CDMO support. 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