Wednesday, July 10, 2013 7:02:09 PM
Looks like OMTH filed the NDA yesterday, here is article today about AZN's very late to the table plans for their Lovaza clone - wonder how much the license fee owed Chrysalis Pharma is? Note that AZN also intends to run a R-IT trial, ours will be over before they even get started!
http://www.nasdaq.com/article/omthera-seeks-fda-approval-for-epanova-analyst-blog-cm258561
Omthera Pharmaceuticals, Inc. ( OMTH ) recently (7/9/2013) submitted a new drug application (NDA) for its cholesterol management candidate, Epanova. Omthera is seeking US Food and Drug Administration (FDA) approval of Epanova for the treatment of patients with severe hypertriglyceridemia.
The NDA was based on encouraging efficacy data from two phase III studies (EVOLVE and ESPRIT), conducted under the FDA's Special Protocol Assessment (SPA) program in 2012.
We note that in May 2013, AstraZeneca ( AZN ) had announced its intention to purchase Omthera for approximately $323 million or $12.70 per share. Moreover, Omthera shareholders will get contingent value rights of up to approximately $120 million, subject to the achievement of Epanova milestones.
The transaction is expected to close by the third quarter of 2013 subject to regulatory approvals. AstraZeneca expects to file a supplemental NDA for Epanova for mixed dyslipidemia as soon as possible. AstraZeneca also intends to get Epanova approved as a fixed dose combination with its cardiovascular drug, Crestor, for mixed dyslipidemia patients with high risk of cardiovascular events. Moreover, AstraZeneca is planning to conduct a large scale cardiovascular outcomes trial to assess Epanova in combination with statins.
We note that on Nov 13, 2009, Omthera entered into an exclusive license agreement with Chrysalis Pharma under which it acquired an exclusive global license for the development, manufacture, and commercialization of Epanova.
http://www.nasdaq.com/article/omthera-seeks-fda-approval-for-epanova-analyst-blog-cm258561
Omthera Pharmaceuticals, Inc. ( OMTH ) recently (7/9/2013) submitted a new drug application (NDA) for its cholesterol management candidate, Epanova. Omthera is seeking US Food and Drug Administration (FDA) approval of Epanova for the treatment of patients with severe hypertriglyceridemia.
The NDA was based on encouraging efficacy data from two phase III studies (EVOLVE and ESPRIT), conducted under the FDA's Special Protocol Assessment (SPA) program in 2012.
We note that in May 2013, AstraZeneca ( AZN ) had announced its intention to purchase Omthera for approximately $323 million or $12.70 per share. Moreover, Omthera shareholders will get contingent value rights of up to approximately $120 million, subject to the achievement of Epanova milestones.
The transaction is expected to close by the third quarter of 2013 subject to regulatory approvals. AstraZeneca expects to file a supplemental NDA for Epanova for mixed dyslipidemia as soon as possible. AstraZeneca also intends to get Epanova approved as a fixed dose combination with its cardiovascular drug, Crestor, for mixed dyslipidemia patients with high risk of cardiovascular events. Moreover, AstraZeneca is planning to conduct a large scale cardiovascular outcomes trial to assess Epanova in combination with statins.
We note that on Nov 13, 2009, Omthera entered into an exclusive license agreement with Chrysalis Pharma under which it acquired an exclusive global license for the development, manufacture, and commercialization of Epanova.
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