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2168 Postings, 4586 Tage MagnetfeldfredyAmarin

29.08.20 15:00
Amarins, Top-Meldung, bahnbrechend:

VASCEPA® (Icosapent Ethyl) Reported to Significantly Reduce Coronary Plaque in EVAPORATE Study Final Results Presented at ESC Congress 2020
Amarin Corporation plc
,GlobeNewswire•August 29, 2020

Primary endpoint of slowed coronary plaque progression reported to have been met with VASCEPA

Significant coronary plaque regression of low attenuation plaque (LAP) reported with VASCEPA provides further insight to potential mechanisms of action

VASCEPA is the first and only agent studied on top of statins reported to exhibit coronary plaque regression in hypertriglyceridemic patients

DUBLIN, Ireland and BRIDGEWATER, N.J., Aug. 29, 2020 (GLOBE NEWSWIRE) -- Amarin Corporation plc (NASDAQ:AMRN) today announced that the trial results from Effect of Icosapent Ethyl on Progression of Coronary Atherosclerosis in Patients with Elevated Triglycerides on Statin Therapy: Final results of the EVAPORATE Trial were presented at ESC Congress 2020, the annual meeting of the European Society of Cardiology, on August 29, 2020, 9:13 am CEST (Central European Summer Time) by Matthew Budoff, M.D., Director of Cardiovascular CT at The Lundquist Institute and Professor of Medicine at the David Geffen School of Medicine at UCLA, the study sponsor. VASCEPA® (icosapent ethyl) demonstrated significant, 17% regression of low attenuation plaque (LAP) volume on multidetector computed tomography (MDCT) compared with placebo over 18 months. As referenced below, these final results can be found in the concurrent publication in European Heart Journal.

“EVAPORATE provides important mechanistic data on coronary plaque characteristics that are potentially relevant to the overall REDUCE-IT® results and clinical use of icosapent ethyl,” commented Matthew Budoff, M.D., Director of Cardiovascular CT at The Lundquist Institute and Professor of Medicine at the David Geffen School of Medicine at UCLA. “The REDUCE-IT REVASC analysis presented at American Society for Preventive Cardiology last month reported an early coronary revascularization benefit signal with sustained statistical significance attained by 11 months. EVAPORATE is the first demonstration of imaging results with icosapent ethyl using MDCT. The coronary plaque reduction shown in EVAPORATE is consistent with the benefits of icosapent ethyl in cardiovascular event outcomes shown in REDUCE-IT, a separate study.”

A total of 80 patients were enrolled in the randomized, double-blind, placebo-controlled EVAPORATE trial. Patients had to have coronary atherosclerosis as documented by MDCT (1 or more angiographic stenoses with ≥20% narrowing), be on statin therapy, and have persistently elevated triglyceride (TG) levels (mean TG at baseline was 259.1 mg/dL [+/- 78.1]). Patients underwent an interim scan at 9 months and a final scan at 18 months. The prespecified primary endpoint was a comparison of change in LAP volume at 18 months between icosapent ethyl and placebo. EVAPORATE was not powered for long-term outcomes.

The final results showed a significant reduction in the primary endpoint; icosapent ethyl reduced LAP plaque volume by 17% from baseline to the 18-month scan, whereas there was a progression of LAP plaque volume in the placebo group. There were significant differences between icosapent ethyl and placebo at study end for secondary endpoints of other types of plaque volume changes, including and sequentially total, total non-calcified, fibrofatty, and fibrous plaque volumes. All regressed in the icosapent ethyl group and progressed in the placebo group, (p<0.01 for all). The only secondary endpoint which did not achieve a significant difference between groups in multivariable modeling was dense calcium (p=0.053).  

The mineral oil placebo, used for consistency with REDUCE-IT, was also analyzed against plaque changes from baseline in another placebo in a separate study. Rates of plaque changes in patients randomized to mineral oil (the placebo cohort) in the EVAPORATE study were compared with rates of plaque changes in the placebo arm of a second study that used a cellulose-based placebo. There was no difference in plaque progression between mineral oil and cellulose based placebos.1

“Coronary plaque regression is an important finding with VASCEPA and may explain, in part, the substantial cardiovascular benefit seen in REDUCE-IT,” said Craig Granowitz, M.D., Ph.D., Amarin’s senior vice president and chief medical officer. “The EVAPORATE study results potentially shed further light on how VASCEPA works to lower residual cardiovascular risk.”

Limitations of this single study include a small sample size. More study is needed to demonstrate the effects of VASCEPA on coronary plaque to determine the relationship of such effects, if any, on cardiovascular risk reduction.

The presentation will be available here with a concurrent publication in European Heart Journal.

Financial Disclosure
Funding from Amarin was provided to the sponsor of the EVAPORATE study, The Lundquist Institute, for Dr. Matthew Budoff’s work on the study.

About Amarin
Amarin Corporation plc is a rapidly growing, innovative pharmaceutical company focused on developing and commercializing therapeutics to cost-effectively improve cardiovascular health. Amarin’s lead product, VASCEPA® (icosapent ethyl), is available by prescription in the United States, Canada, Lebanon and the United Arab Emirates. VASCEPA is not yet approved and available in any other countries. Amarin, on its own or together with its commercial partners in select geographies, is pursuing additional regulatory approvals for VASCEPA in China, Europe and the Middle East. For more information about Amarin, visit

About Cardiovascular Risk
The number of deaths in the United States attributed to cardiovascular disease continues to rise. There are 605,000 new and 200,000 recurrent heart attacks per year (approximately 1 every 40 seconds), in the United States. Stroke rates are 795,000 per year (approximately 1 every 40 seconds), accounting for 1 of every 19 U.S. deaths. Cardiovascular disease results in 859,000 deaths per year in the United States.2 In aggregate, there are more than 2.4 million major adverse cardiovascular events per year from cardiovascular disease or, on average, 1 every 13 seconds in the United States alone.

Controlling bad cholesterol, also known as LDL-C, is one way to reduce a patient’s risk for cardiovascular events, such as heart attack, stroke or death. However, even with the achievement of target LDL-C levels, millions of patients still have significant and persistent risk of cardiovascular events, especially those patients with elevated triglycerides. Statin therapy has been shown to control LDL-C, thereby reducing the risk of cardiovascular events by 25-35%.3 Significant cardiovascular risk remains after statin therapy. People with elevated triglycerides have 35% more cardiovascular events compared to people with normal (in range) triglycerides taking statins.4,5,6

REDUCE-IT was a global cardiovascular outcomes study designed to evaluate the effect of VASCEPA in adult patients with LDL-C controlled to between 41-100 mg/dL (median baseline 75 mg/dL) by statin therapy and various cardiovascular risk factors including persistent elevated triglycerides between 135-499 mg/dL (median baseline 216 mg/dL) and either established cardiovascular disease (secondary prevention cohort) or diabetes mellitus and at least one other cardiovascular risk factor (primary prevention cohort).

REDUCE-IT, conducted over seven years and completed in 2018, followed 8,179 patients at over 400 clinical sites in 11 countries with the largest number of sites located within the United States. REDUCE-IT was conducted based on a special protocol assessment agreement with FDA. The design of the REDUCE-IT study was published in March 2017 in Clinical Cardiology.7 The primary results of REDUCE-IT were published in The New England Journal of Medicine in November 2018.8 The total events results of REDUCE-IT were published in the Journal of the American College of Cardiology in March 2019.9 These and other publications can be found in the R&D section on the company’s website at

About VASCEPA® (icosapent ethyl) Capsules
VASCEPA (icosapent ethyl) capsules are the first-and-only prescription treatment approved by the FDA comprised solely of the active ingredient, icosapent ethyl (IPE), a unique form of eicosapentaenoic acid. VASCEPA was initially launched in the United States in 2013 based on the drug’s initial FDA approved indication for use as an adjunct therapy to diet to reduce triglyceride levels in adult patients with severe (≥500 mg/dL) hypertriglyceridemia. Since launch, VASCEPA has been prescribed over eight million times. VASCEPA is covered by most major medical insurance plans. The new, cardiovascular risk indication for VASCEPA was approved by the FDA in December 2019.

Indications and Limitation of Use
VASCEPA is indicated:

   As an adjunct to maximally tolerated statin therapy to reduce the risk of myocardial infarction, stroke, coronary revascularization and unstable angina requiring hospitalization in adult patients with elevated triglyceride (TG) levels (≥ 150 mg/dL) and
       established cardiovascular disease or
       diabetes mellitus and two or more additional risk factors for cardiovascular disease.
   As an adjunct to diet to reduce TG levels in adult patients with severe (≥ 500 mg/dL) hypertriglyceridemia.

The effect of VASCEPA on the risk for pancreatitis in patients with severe hypertriglyceridemia has not been determined.

Important Safety Information

   VASCEPA is contraindicated in patients with known hypersensitivity (e.g., anaphylactic reaction) to VASCEPA or any of its components.
   VASCEPA was associated with an increased risk (3% vs 2%) of atrial fibrillation or atrial flutter requiring hospitalization in a double-blind, placebo-controlled trial. The incidence of atrial fibrillation was greater in patients with a previous history of atrial fibrillation or atrial flutter.
   It is not known whether patients with allergies to fish and/or shellfish are at an increased risk of an allergic reaction to VASCEPA. Patients with such allergies should discontinue VASCEPA if any reactions occur.
   VASCEPA was associated with an increased risk (12% vs 10%) of bleeding in a double-blind, placebo-controlled trial. The incidence of bleeding was greater in patients receiving concomitant antithrombotic medications, such as aspirin, clopidogrel or warfarin.
   Common adverse reactions in the cardiovascular outcomes trial (incidence ≥3% and ≥1% more frequent than placebo): musculoskeletal pain (4% vs 3%), peripheral edema (7% vs 5%), constipation (5% vs 4%), gout (4% vs 3%), and atrial fibrillation (5% vs 4%).
   Common adverse reactions in the hypertriglyceridemia trials (incidence >1% more frequent than placebo): arthralgia (2% vs 1%) and oropharyngeal pain (1% vs 0.3%).
   Adverse events may be reported by calling 1-855-VASCEPA or the FDA at 1-800-FDA-1088.
   Patients receiving VASCEPA and concomitant anticoagulants and/or anti-platelet agents should be monitored for bleeding.

Key clinical effects of VASCEPA on major adverse cardiovascular events are included in the Clinical Studies section of the prescribing information for VASCEPA, as set forth below:

Effect of VASCEPA on Time to First Occurrence of Cardiovascular Events in Patients with
Elevated Triglyceride levels and Other Risk Factors for Cardiovascular Disease in REDUCE-IT
vs Placebo
N = 4089
n (%) Incidence Rate
(per 100 patient years) N = 4090
n (%) Incidence Rate
(per 100 patient years) Hazard Ratio (95% CI)
Primary composite endpoint
Cardiovascular death, myocardial infarction, stroke, coronary revascularization, hospitalization for unstable angina (5-point MACE) 705
(17.2) 4.3 901
(22.0) 5.7 0.75
(0.68, 0.83)
Key secondary composite endpoint
Cardiovascular death, myocardial infarction, stroke (3-point MACE) 459
(11.2) 2.7 606
(14.8) 3.7 0.74
(0.65, 0.83)
Other secondary endpoints
Fatal or non-fatal myocardial infarction 250
(6.1) 1.5 355
(8.7) 2.1 0.69
(0.58, 0.81)
Emergent or urgent coronary revascularization 216
(5.3) 1.3 321
(7.8) 1.9 0.65
(0.55, 0.78)
Cardiovascular death [1] 174
(4.3) 1.0 213
(5.2) 1.2 0.80
(0.66, 0.98)
Hospitalization for unstable angina [2] 108
(2.6) 0.6 157
(3.8) 0.9 0.68
(0.53, 0.87)
Fatal or non-fatal stroke 98
(2.4) 0.6 134
(3.3) 0.8 0.72
(0.55, 0.93)
[1] Includes adjudicated cardiovascular deaths and deaths of undetermined causality.
[2] Determined to be caused by myocardial ischemia by invasive/non-invasive testing and requiring emergent hospitalization.


Forward-Looking Statements
This press release contains forward-looking statements, including statements regarding the potential impact of VASCEPA in various clinical uses. These forward-looking statements are not promises or guarantees and involve substantial risks and uncertainties. Among the factors that could cause actual results to differ materially from those described or projected herein include the following: uncertainties associated generally with research and development and clinical trials such as further clinical evaluations failing to confirm earlier findings. A further list and description of these risks, uncertainties and other risks associated with an investment in Amarin can be found in Amarin's filings with the U.S. Securities and Exchange Commission, including its most recent Quarterly Report on Form 10-Q. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. Amarin undertakes no obligation to update or revise the information contained in this press release, whether as a result of new information, future events or circumstances or otherwise. Amarin’s forward-looking statements do not reflect the potential impact of significant transactions the company may enter into, such as mergers, acquisitions, dispositions, joint ventures or any material agreements that Amarin may enter into, amend or terminate.

Availability of Other Information About Amarin
Investors and others should note that Amarin communicates with its investors and the public using the company website (, the investor relations website (, including but not limited to investor presentations and investor FAQs, Securities and Exchange Commission filings, press releases, public conference calls and webcasts. The information that Amarin posts on these channels and websites could be deemed to be material information. As a result, Amarin encourages investors, the media, and others interested in Amarin to review the information that is posted on these channels, including the investor relations website, on a regular basis. This list of channels may be updated from time to time on Amarin’s investor relations website and may include social media channels. The contents of Amarin’s website or these channels, or any other website that may be accessed from its website or these channels, shall not be deemed incorporated by reference in any filing under the Securities Act of 1933.

Amarin Contact Information
Investor Inquiries:
Elisabeth Schwartz
Investor Relations
Amarin Corporation plc
In U.S.: +1 (908) 719-1315 (investor inquiries)

Lee M. Stern
Solebury Trout
In U.S.: +1 (646) 378-2992

Media Inquiries:
Alina Kolomeyer
Amarin Corporation plc
In U.S.: +1 (908) 892-2028 (media inquiries)


1   Lakshmanan S, Shekar C, Kinninger A, et al. Comparison of mineral oil and non-mineral oil placebo on coronary plaque progression by coronary computed tomography angiography. Cardiovasc Res. 2020;116(3):479-482.

2   American Heart Association. Heart Disease and Stroke Statistics—2020 Update: A Report From the American Heart Association. Circulation. 2020;141:e139–e596.

3   Ganda OP, Bhatt DL, Mason RP, et al. Unmet need for adjunctive dyslipidemia therapy in hypertriglyceridemia management. J Am Coll Cardiol. 2018;72(3):330-343.

4   Budoff M. Triglycerides and triglyceride-rich lipoproteins in the causal pathway of cardiovascular disease. Am J Cardiol. 2016;118:138-145.

5   Toth PP, Granowitz C, Hull M, et al. High triglycerides are associated with increased cardiovascular events, medical costs, and resource use: A real-world administrative claims analysis of statin-treated patients with high residual cardiovascular risk. J Am Heart Assoc. 2018;7(15):e008740.

6   Nordestgaard BG. Triglyceride-rich lipoproteins and atherosclerotic cardiovascular disease - New insights from epidemiology, genetics, and biology. Circ Res. 2016;118:547-563.

7   Bhatt DL, Steg PG, Brinton E, et al., on behalf of the REDUCE-IT Investigators. Rationale and Design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial. Clin Cardiol. 2017;40:138-148.

8   Bhatt DL, Steg PG, Miller M, et al., on behalf of the REDUCE-IT Investigators. Cardiovascular Risk Reduction with Icosapent Ethyl for Hypertriglyceridemia. N Engl J Med. 2019;380:11-22.

9   Bhatt DL, Steg PG, Miller M, et al., on behalf of the REDUCE-IT Investigators. Reduction in first and total ischemic events with icosapent ethyl across baseline triglyceride tertiles. J Am Coll Cardiol. 2019;74:1159-1161.


2168 Postings, 4586 Tage MagnetfeldfredyAmarin

29.08.20 15:25  

2168 Postings, 4586 Tage MagnetfeldfredyAmarin

29.08.20 15:34
Hier die Topergebnisse in einer tollen Tabelle:

Angehängte Grafik:
evaporate_final_results__29.png (verkleinert auf 49%) vergrößern

718 Postings, 1741 Tage Ice-Nine comingKeiner zweifelt ...

30.08.20 11:32
... an der Effektivität von Vascepa. Nicht die Mediziner und auch nicht "der Markt".

Aber solange der Patentstreit nicht doch noch gut für AMRN endet, werden derlei News wie hier gepostet, keine Sau interessieren. Leider!  

2168 Postings, 4586 Tage MagnetfeldfredyAmarin

30.08.20 12:55
Fresh data reveals that the arteries of those given a twice-daily capsule of Vascepa - a type of highly purified omega-3 fatty acid - became progressively clearer over time.
Du hast keine Ahnung, der Patentstreit betrifft nur die USA,  Europa steht vor der Zulassung mit 10-jähriger Exklusivität und mit solchen Meldungen kann sehr schnell ein short squeeeeeeeeeeezzee kommen, da am 2.9.2020 auch noch das hearing der oral arguments stattfindet, mit Mr. Singer, dem weltbesten Patentanwalt, da wird sich Schlizauge Du noch umsehen und Du auch......

Es interessiert keine Sau, aha nur Yello Press berichtet schon:

How a humble herring is bringing hope to millions by helping to heal hearts through a new drug that unblocks coronary arteries

   It is the first time a drug has been shown to turn back the physiological clock
   Drug was sourced from species of herring fished off Chile and Argentina coasts
   Data shows arteries of those given capsule twice a day became clearer over time

By Stephen Adams Medical Editor For The Mail On Sunday

Published: 01:42 BST, 30 August 2020 | Updated: 01:55 BST, 30 August 2020




View comments

A new drug derived from a herring found in the South Pacific unblocks coronary arteries – bringing hope to millions of people with serious heart disease.

It is the first time a drug has been shown to turn back the physiological clock rather than slowing the furring of arteries.

Fresh data being presented at the European Society of Cardiology’s virtual meeting this weekend reveals that the arteries of those given a twice-daily capsule of Vascepa – a type of highly purified omega-3 fatty acid – became progressively clearer over time.
A new drug derived from a herring found in the South Pacific unblocks coronary arteries ¿ bringing hope to millions of people with serious heart disease (file photo)

A new drug derived from a herring found in the South Pacific unblocks coronary arteries – bringing hope to millions of people with serious heart disease (file photo)


   Now a single blood test can diagnose the gluten illness that...
   HEALTH NOTES: New 'gargle-and-spit' test spots Covid-19 in a...

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Dr Craig Granowitz, chief medical officer of the drug’s manufacturer Amarin Corporation, said it was sourced from a species of herring fished off the coasts of Chile and Argentina.

He said the same results could not be obtained from taking omega-3 food supplements.

Scans showed the volume of unstable plaque in two major coronary arteries of 80 volunteers on Vascepa fell by an average of 17 per cent over an 18-month period.
Fresh data reveals that the arteries of those given a twice-daily capsule of Vascepa became progressively clearer over time (file photo)

Fresh data reveals that the arteries of those given a twice-daily capsule of Vascepa became progressively clearer over time (file photo)

In those given placebo pills, the volume more than doubled.

Dr Granowitz said: ‘A cardiovascular event is a plumbing problem: a piece of junk gets stuck in your [arterial] pipe. The key [to good cardiovascular health] is good flow.’

Vascepa was approved by the US Food and Drugs Administration last December and is now awaiting approval from Euro-pean authorities.  

8302 Postings, 1562 Tage VassagoAMRN 7.36$

30.08.20 17:00

Patent-Berufungsverhandlung für Mittwoch angesetzt

Man darf gespannt sein, ob und welche Entscheidungen getroffen werden.


718 Postings, 1741 Tage Ice-Nine comingre #456

30.08.20 18:49
Es ist ja die erste mündliche Anhörung. Meines Wissens nach rechnet die Company im Q1 mit einer Entscheidung. Hast du Kenntnisse darüber, dass es seitens des Gerichtes zu einem früheren Urteil kommen könnte?  

718 Postings, 1741 Tage Ice-Nine comingRichter

02.09.20 15:36
Die Auswahl der Richter hat bei Bekanntgabe heute morgen nicht gerade für Begeisterung gesorgt.....mal wabwrten  

570 Postings, 2374 Tage RV10Aus die Maus. Das war's!

02.09.20 17:26


8302 Postings, 1562 Tage VassagoAMRN 5.25$ (-28%)

02.09.20 17:26
Ist das die Nervosität vor der Entscheidung oder ist schon etwas durchgesickert? Spannend!  

718 Postings, 1741 Tage Ice-Nine comingLäuft :-))))

02.09.20 17:31
Na, Humor ist, wenn man dennoch lacht.....

Obgleich sich meine Position in AMRN nun aktuell halbiert hat, ist sie immer noch einer meiner Top 2 Positionen. Jo, war risikotechnisch zu groß die Position. LOL.

Mal sehen, ob ich nachlege ... die Verkaufszahlen in den USA werden auch im Falle der Niederlage vor Gericht sowie ex-USA ja dennoch positiv ausfallen. Imho zu positiv in Relation zum aktuellen Kurs.

Aber ok, wie Gogomagneto oben schon schrieb: ich habe von AMRN ohnehin keine Ahnung. Insofern: do your on due diligence, please! ;-)))))  

8302 Postings, 1562 Tage VassagoAMRN 5.15$

02.09.20 17:47

Die Auswahl der Richter stimmt die Analysten skeptisch


718 Postings, 1741 Tage Ice-Nine comingMp3

02.09.20 18:22
Auf Twitter kommentierte @danravicher die Verhandlung. Kenne den nicht, insofern habe ich keine Meinung zu def Aussagekraft seiner Bemerkungen.

Ganz interessant: Wer will, kann sich am Ende des Tages / Morgen (?) die Verhandlung als Audio-Recording anhören.  

1149 Postings, 5232 Tage CullarioAmarin

02.09.20 21:19
Kann mich jemand kurz aufs Laufende bringen, um was es hier geht?  

8302 Postings, 1562 Tage VassagoAMRN 5.04$ (-31%)

03.09.20 13:47


Also wenn es nach Dan Ravicher geht, ist die Anhörung klar zu Ungunsten von Amarin gelaufen. Er begründet das damit, dass die Richter keine einzige Frage an den Anwalt der Gegenseite (Hikma/Dr. Reddy´s) stellte und wertet dies als "Zustimmung". Dan Ravicher ist Rechtsprofessor und scheint solche Anhörungen oft zu beobachten.

Von den drei Richtern:  Timothy Dyk, Jimmie V. Reyna and Todd Hughes, soll besonders Dyk den Anwalt von Amarin hart in die Mangel genommen haben. Es wird vermutet, dass Dyk gegen Amarin stimmen wird. Die anderen beiden Richter sind für die Beobachter extrem schwer einzuschätzen.

Die MP3 der Anhörung ist online verfügbar

Meiner Einschätzung nach stehen die Chancen 30/70 das Amarin die Berufung gewinnt, vermutlich eher schlechter. Wo könnte AMRN stehen wenn sie die Berufung verlieren? Vermutlich bei 2-4$. Sollte AMRN gewinnen, sehe ich die Aktie bei >10$. Muss jeder selber wissen, ob es ihm das Risiko wert ist.

Die wichtigste Frage für mich ist, ob dieses Verfahren sich in der höchsten Instanz befindet oder ob Amarin im Falle einer Negativentscheidung noch die Möglichkeit hat ein höheres Gericht anzurufen?

Manche Analysten deuten an, dass AMRN noch das Europageschäft bliebe bzw. eine Unternehmensverkauf auch eine Option sein könnte. Ich stelle mir die Frage, ob Amarin nicht alternativ mit Hikma und Dr. Reddy´s hätte einen Vergleich erzielen können die Markteinführung des Generikas um 10 Jahre zu verschieben.

Solche Vereinbarungen gibt es z.B schon mit Teva und Apotex.


718 Postings, 1741 Tage Ice-Nine comingUrteil raus?

03.09.20 15:15
Wenn man sich den Kurs anschaut, ist soeben das Urteil rausgekommen....  

718 Postings, 1741 Tage Ice-Nine comingWo ist ...

03.09.20 15:16
Magneto wenn man ihn braucht.... seufz..... tough times.....  

570 Postings, 2374 Tage RV10Patente sind ungültig

03.09.20 15:18


718 Postings, 1741 Tage Ice-Nine comingJo, ist leider so.....

03.09.20 15:23

570 Postings, 2374 Tage RV10Kurs wurde gestoppt

03.09.20 15:36


718 Postings, 1741 Tage Ice-Nine comingWert ROW

03.09.20 15:38
Wenn man manchen Rechnungen bezüglich der künftigen US- sowie der Rest-of-the-World Umsätze für Vascepa Glauben schenken mag, dann sind die aktuellen Kursregionen Schnäppchenkurse.

Schauen wir mal ....  

718 Postings, 1741 Tage Ice-Nine comingre #470

03.09.20 15:41
Läuft wieder ....  

8302 Postings, 1562 Tage VassagoAMRN 5.02$

03.09.20 16:06
Scheint in der Kursen von gestern schon eingepreist gewesen zu sein.  

718 Postings, 1741 Tage Ice-Nine comingAmarin statement:

03.09.20 16:56

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