Wednesday, January 22, 2014 7:29:59 PM
AMRN is Dead Money....this company has no choice but to wait for Reduce-It. Every other suggestion from all of us disappointed investors on this board is just wishful thinking. Litigation, if it's expedited, will easily take 2 or even 3 years to get through the legal system to verdict. Probably longer than that. AMRN is going through the channel of appeals in FDA, so from my understanding that will take the remainder of 2014. Add that to the three years of litigation which commences after the appeals are exhausted and you're in 2018. Reduce it will have spoken by then.
FDA is not listening, not negotiating, and just simply does not care. You want proof: they delayed their decision on 1/15, which was their own deadline that they set after they missed the first deadline. Clearly this was not to examine any details or reconsider the facts. They delayed because they just didn't care enough to get around to saying no on 1/15. There was no further in depth analysis, no great insight, and most clearly no change of heart. FDA is feeling no pressure from the appeals process, threatened litigation, the CP, the epadruginitiative, or the threat to discontinue Reduce it.
It couldn't be clearer that there will be no positive news from FDA on Vascepa,ever. There will be no fruitful discussions, negotiations or threats that result in action. AMRN as a company, is at the bottom of the river with a cement block chained to it's ankle. There will be no partners or buyouts. There will be no change to the label or usage indication. All that's left is Reduce It. And Reduce It has to show positive results in reducing CVD events or else this company is toast. The odds of this happening are very small. Deep down we all know its not likely that reducing trigs is enough to significantly impact reducing cvd deaths. Reduce-it is not about helping inflammation, reducing dry eyes or all of the other great things Vascepa may be able to do. The objective is to reduce death, and based on that alone Vascepa likely will not be significant enough for FDA to expand usage. BP is in control and FDA has spoken. They are not mixing words. They are not being coy. They are crystal clear. This is dead money for at least 2+ years and the odds of success at that time are minute.
I am holding this useless stock because it is trading at fair value based upon current usage and cash on hand and mostly because I don't have much too money left in it to lose. I am not optimistic in the least that I will ever make any money back to help make up my 75% loss. You shouldn't be either. We need to face reality.....AMRN is dead money. You will have better upside in a savings account at your local bank.
FDA is not listening, not negotiating, and just simply does not care. You want proof: they delayed their decision on 1/15, which was their own deadline that they set after they missed the first deadline. Clearly this was not to examine any details or reconsider the facts. They delayed because they just didn't care enough to get around to saying no on 1/15. There was no further in depth analysis, no great insight, and most clearly no change of heart. FDA is feeling no pressure from the appeals process, threatened litigation, the CP, the epadruginitiative, or the threat to discontinue Reduce it.
It couldn't be clearer that there will be no positive news from FDA on Vascepa,ever. There will be no fruitful discussions, negotiations or threats that result in action. AMRN as a company, is at the bottom of the river with a cement block chained to it's ankle. There will be no partners or buyouts. There will be no change to the label or usage indication. All that's left is Reduce It. And Reduce It has to show positive results in reducing CVD events or else this company is toast. The odds of this happening are very small. Deep down we all know its not likely that reducing trigs is enough to significantly impact reducing cvd deaths. Reduce-it is not about helping inflammation, reducing dry eyes or all of the other great things Vascepa may be able to do. The objective is to reduce death, and based on that alone Vascepa likely will not be significant enough for FDA to expand usage. BP is in control and FDA has spoken. They are not mixing words. They are not being coy. They are crystal clear. This is dead money for at least 2+ years and the odds of success at that time are minute.
I am holding this useless stock because it is trading at fair value based upon current usage and cash on hand and mostly because I don't have much too money left in it to lose. I am not optimistic in the least that I will ever make any money back to help make up my 75% loss. You shouldn't be either. We need to face reality.....AMRN is dead money. You will have better upside in a savings account at your local bank.
Recent AMRN News
- Amarin Highlights New REDUCE-IT Analysis Showing Risk-Weighted ApoB May Improve Cardiovascular Risk Detection (AMRN) • IH Market News • 05/27/2026 03:24:38 PM
- New REDUCE-IT® Analysis Presented at the European Atherosclerosis Society (EAS) Congress 2026 Suggests Risk-Weighted ApoB May Improve Identification of Residual Cardiovascular Risk in Statin-Treated Patients with Hypertriglyceridemia • GlobeNewswire Inc. • 05/27/2026 12:00:00 PM
- Earnings Report Shows Narrowing Losses as Amarin (AMRN) Advances Partner-Led Growth Strategy • IH Market News • 04/29/2026 02:19:17 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 04/29/2026 11:06:34 AM
- Form 8-K - Current report • Edgar (US Regulatory) • 04/29/2026 11:05:15 AM
- Amarin Reports 2026 First Quarter Financial Results • GlobeNewswire Inc. • 04/29/2026 11:00:00 AM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/22/2026 09:00:06 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:07 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:05 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:04 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:04 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:03 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:02 PM
- Amarin to Report First Quarter 2026 Financial Results and Host Conference Call on April 29, 2026 • GlobeNewswire Inc. • 04/15/2026 12:00:00 PM
- Form ARS - Annual Report to Security Holders • Edgar (US Regulatory) • 04/10/2026 09:01:34 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 04/10/2026 09:00:20 PM
- American College of Cardiology (ACC) Scientific Sessions 2026 Underscore the Need for Complementary Therapies Including Icosapent Ethyl (IPE) in Treatment of Elevated Triglycerides and Cardiovascular Risk Reduction • GlobeNewswire Inc. • 04/08/2026 12:00:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/02/2026 08:30:11 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 03/30/2026 09:57:06 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/27/2026 09:00:07 PM
- Amarin Highlights Guideline Recommended Role of Icosapent Ethyl in Managing Cardiovascular Risk Following Release of Updated 2026 ACC/AHA/Multisociety Dyslipidemia Guideline • GlobeNewswire Inc. • 03/18/2026 12:30:00 PM
- New REDUCE-IT Data in Patients at Extreme Cardiovascular Risk and In Vitro Research on the Mechanistic Effects of Eicosapentaenoic Acid (EPA) on Lipoprotein(a) [Lp(a)] Oxidation to be Presented at the American College of Cardiology’s (ACC) Annual Scienti • GlobeNewswire Inc. • 03/16/2026 12:15:00 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 03/02/2026 10:31:01 PM
- Effects of Icosapent Ethyl on Risk and Duration of Hospitalizations and Death in REDUCE-IT® Post Hoc Analysis Published in the European Journal of Preventive Cardiology • GlobeNewswire Inc. • 03/02/2026 01:00:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/25/2026 12:05:26 PM
