Geld verdienen mit kleineren amerikanischen Biotec

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29.01.06 19:20 #1 Geld verdienen mit kleineren amerikanischen Biote.
 
Geld verdienen mit kleineren amerikanischen Biotechs

26. Januar 2006 Biotech-Fonds sind aus der Mode geraten und haben nach dem Boom-Jahr 2000 seit 2001 unter dem Strich nur Mittel verloren, obwohl sie binnen Jahresfrist einen durchschnittlichen Ertrag von 26 Prozent geliefert haben. Doch es gibt Ausnahmen, die Geld erhalten und gebracht haben. Zum Beispiel der FCP OP Medical BioHealth-Fonds. Betreut wird das Produkt aus dem Hause Oppenheim Pramerica, der Gemeinschaftsfirma von Sal.Oppenheim und Prudential Financial, von Michael Fischer. Der Inhaber der Medical Strategy GmbH mit Sitz in München kann auf eine Erfolgsgeschichte verweisen.

In den vergangenen fünf Jahren hat er um gut 28 Prozent zugelegt. Kein anderer weltweit anlegender Biotech-Fonds konnte in diesem Zeitraum Kurszuwächse erwirtschaften - und sei es auch noch so kleine. Die nächst besten Wettbewerber, der DWS Invest Biotech LC und der Espa Stock Biotech, haben Kursverluste von annähernd zwei Prozent im ersten Fall und von gut 14 Prozent im zweiten Fall zu Buche stehen. Auch im Dreijahresvergleich hat Fischer seine Konkurrenten abgehängt.


Dumm nur: In den vergangenen Jahren konnte er seine Erfolgsgeschichte unter Fondskäufern in Deutschland nicht streuen. Denn der FCP OP Medical BioHealth war hierzulande nicht zugelassen. Doch seit Mitte Dezember ist das anders. Nun legt er sein Konzept dar - und hat auch keine Probleme zu erklären, warum die Performance in den vergangenen zwölf Monaten nicht so toll war wie in den Vorjahren und sein von Standard & Poor's mit einem AA-Rating geschmückte Fonds auf Platz 13 unter 34 Branchenvertretern gerutscht ist. Und er ist zuversichtlich, Anfang 2007 wieder besser dazustehen.

Hälfte des Kapitals steckt in mittelgroßen Werten

Biotech-Werte stehen aus Sicht von Fischer „vor dem erneuten Durchbruch”. Wobei er kleinere und mittlere amerikanische Unternehmen meint. „Dort drüben spielt bei Biotechs die Musik”, sagt er. Börsennotierten deutschen Branchenvertretern wie GPC, Medigene, Morphosys oder Paion steht er nach eigenen Worten sehr zurückhaltend gegenüber. Begründung: Das Chance/Risiko-Verhältnis sei einfach schlechter als bei amerikanischen Firmen.


Die vergleichsweise geringe Marktkapitalisierung deutscher Unternehmen ist dagegen erklärtermaßen kein Minuspunkt: „Wir investieren auch in Firmen mit einem Börsenwert unter 100 Millionen Dollar”. Knapp die Hälfte des Fondsvolumens von 146,2 Millionen Euro (179 Millionen Dollar) steckt nach Angaben von Oppenheim Pramerica in Unternehmen, die mit weniger als 500 Millionen Dollar bewertet sind und nur elf Prozent in „Dickschiffen”, die derzeit mehr als 1,5 Milliarden Dollar wert sind.

„Big Caps inzwischen zu teuer für große Kurszuwächse”

Diese Verteilung ist nach Worten von Fischer auch die Ursache für das relativ schwächere Abschneiden im Jahr 2005. Denn in den zurückliegenden Monaten schnitten große Biotechs in den Vereinigten Staaten erheblich besser als kleinere und mittlere Werte. Die ersten erreichten demnach einen durchschnittlichen Zuwachs von 25 Prozent, die zweiten ein „Plüschen” von weniger als fünf Prozent. Fischer ficht das aber mit Blick auf die Zukunft nicht an. Vielmehr verweist er auf eine Aussage in dem Magazin „Biocentury”, der „Biotech-Bibel für Anleger”. In der Januar-Aussage heißt es: „Keiner geht davon aus, daß die Biotech Big Caps in diesem Jahr auch nur annähernd nochmals so viel zulegen werden.”

Nun kommt es oft anders, als die Mehrheit an der Börse meint. Doch Fischer führt die Bewertung an, um diese These zu stützen. Titel wie Gilead und Genentech, deren Kurs im vergangenen Jahr jeweils um mehr als 50 Prozent kletterte, seien inzwischen einfach zu teuer - auch wenn in beiden Fällen das Kurs-Gewinn-Verhältnis für 2006 unter dem Wert für 2005 liegt. Ein Konzern wie Amgen oder Genentech, der jetzt mit fast 100 Milliarden Dollar bewertet sei, werde binnen Jahresfrist nicht 200 Milliarden Dollar kosten können.

Höhere Kurse durch Umschichtungen von Anlagekapital

Dabei stehen nach seinen Worten 25 Biotech Big Caps für zwei Drittel des Geldes, das in Biotech-Titeln stecken. Der Rest verteile sich auf rund 300 mittlere und kleinere Firmen. Um deren Aktien zum Laufen zu bringen, bedarf es nach Einschätzung des Fondsberaters nicht einmal mächtiger Umschichtungen aus Big Caps. Für Kurszuwächse bei Biotechs sprechen aus seiner Sicht grundsätzlich eine „Vielzahl von Produkteinführungen, Produktzulassungen und Phase-III-Ergebnissen”, also Berichten, wie sich Wirkstoffe in der letzten und entscheidenden klinischen Testphase geschlagen haben.

Schon am Markt oder kurz vor dem Eintritt in denselben seien ein Nierenkrebsmittel von Onyx und Bayer, das Jahresumsätze von bis zu 750 Millionen Dollar bringen könne, ein von Alkermes und Cephalon entwickeltes Medikament gegen Trunksucht, das gespritzt werde, einen Monat lang das Verlangen nach Alkohol stark dämpfen soll und für Umsätze von bis zu 400 Millionen Dollar gut sei sowie Mittel von Cephalon einerseits und Noven/Shire andererseits gegen das Aufmerksamkeits-Defizit-Syndrom (ADS) bei Kindern, auch bekannt als Hyperaktivität - ein Massenphänomen.

Wiederzugelassen werden soll ein Multiple Sklerose-Medikament von Biogen und Elan. Vor der Genehmigung steht laut Fischer auch ein durch die Nase einzunehmender Grippeimpfstoff von Medimmune. Nicht zuletzt angesichts der Diskussion um die Vogelgrippe sei dies ein interessantes Projekt.

Reiner Stockpicking-Ansatz

Fischer verfolgt bei der Auswahl der Investments keine Indexvorgaben, sondern einen reinen Stockpicking-Ansatz. Das heißt: Er sucht zusammen mit ihm zuarbeitenden Experten gezielt Einzeltitel aus, die aus ihrer Sicht vielversprechend sind. Kauf- und Verkaufentscheidungen liegt demnach ein hauseigenes Bewertungsmodell zugrunde.

Den FCP OP Medical BioHealth gibt es in einer Euro-Version, die nicht währungsbesichert ist (ISIN: LU0119891520), und in einer Euro-Variante, die Kursrisiken durch Schwankungen im Verhältnis von Euro/Dollar ausschließt (ISIN: LU0228344361). Der Ausgabeaufschlag beträgt jeweils fünf Prozent, die Verwaltungsgebühr 1,7 Prozent. Zudem verlangt Oppenheim Pramerica eine sogenannte Performance Fee: Wenn der Fonds einen Wertzuwachs von fünf Prozent oder mehr erreicht, behält die Fondsgesellschaft 15 Prozent des über dieser Grenze liegenden Kursgewinns ein.


Die in dem Beitrag geäußerte Einschätzung gibt die Meinung des Autors und nicht die der F.A.Z.-Redaktion wieder.
 
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23.04.06 06:00 #31 Dynavax to Advance Cancer, Hepatitis Therapy

Dynavax to Advance Cancer, Hepatitis B and Hepatitis C Therapy Programs With $50 Million Funding

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19 April 2006, 4:00pm ET

Collaborative Financing From Symphony Capital Partners, LP Designed to Advance                     Next-Generation TLR-Agonist Pipeline

BERKELEY, Calif., April 19 /PRNewswire-FirstCall/ -- Dynavax Technologies Corporation (Nasdaq: DVAX) announced an agreement with Symphony Capital Partners, LP and its co-investors to provide $50 million of committed capital to advance Dynavax's ISS-based cancer, hepatitis B and hepatitis C therapeutic programs through clinical development.

Under the terms of the agreement, Symphony Capital, a private equity fund, has established Symphony Dynamo, Inc., which will be capitalized initially with $20 million and an additional $30 million within one year following closing to fund Dynavax's identified development programs in cancer and hepatitis therapeutics. Dynavax has granted a license to the intellectual property for the ISS compounds selected for the Symphony Dynamo programs. Through a purchase option, Dynavax retains the exclusive right, but not the obligation, to acquire certain of the programs at specified points in time, or the entire set of funded programs at specified prices during the term of the development period. The term of the agreement is up to five years. The implementation of the development plans will be led by Dynavax with support from RRD International, LLC, Symphony Capital's clinical development partner, to provide additional clinical development and regulatory capabilities for the advancement of Dynavax's cancer, hepatitis B and hepatitis C therapeutic programs.

"We believe that this collaborative financing arrangement is timely and opportune, and fulfills key strategic goals for our company. It will enable us to continue to focus critical resources on advancing our lead programs in ragweed allergy and hepatitis B vaccines and provide additional minimally dilutive funding for investment in our early-stage, second-generation programs. This approach should allow us to build additional value in our pipeline and expand our partnering opportunities, all in a risk-reduced manner," said Dino Dina, MD, president and chief executive officer.

Continued Dr. Dina: "We can now invest more robustly in our cancer and hepatitis therapeutics pipeline, optimize the potential of our second-generation ISS-based technology, and accelerate creation of a new set of partnering assets. With TOLAMBA and HEPLISAV having achieved proof-of-concept and advancing through late-stage clinical trials and potentially toward registration, we believe now is the right time to invest in our cancer, hepatitis B and hepatitis C therapeutic programs. This financing strategy is consistent with our overall corporate strategy to have a steady stream of product opportunities moving into and through the clinic, to advance next-generation programs that represent attractive therapeutic and commercial opportunities, and to generate a meaningful return on investment for our shareholders."

Financial Terms

Funds from the arrangement will be dedicated to Dynavax's cancer product candidate, currently in a Phase 2 trial in Non-Hodgkin's lymphoma and anticipated to advance into clinical trials in solid tumors in 2006, and its hepatitis B and C therapeutic product candidates, which are anticipated to enter the clinic in 2007.

Symphony Dynamo will be capitalized initially with $20 million and an additional $30 million within one year following closing. Dynavax will issue to Symphony Dynamo investors five-year warrants to purchase two million shares of Dynavax common stock at $7.32 per share, representing a 25% premium over the recent 60-day trading range average of $5.86 per share. The term of the warrants is five years and the exercise price is subject to reduction to $5.86 per share under certain circumstances.

Dynavax will have an exclusive option, exercisable at its sole discretion, to acquire all of the programs through the purchase of all of the equity in Symphony Dynamo, exercisable at any time beginning one year after the closing date of the transaction and ending either five years after the closing date or at a time when the funding balance remaining in Symphony Dynamo reaches a certain minimum level. The purchase price is based on a compounded annual rate of return of 27% calculated as of the time of exercise. The purchase option exercise price is payable in cash or a combination of cash and shares of Dynavax common stock, at Dynavax's sole discretion. Dynavax also has an option to purchase either the hepatitis B or hepatitis C program during the first year of the agreement.

Dynavax plans to consolidate the results of operations of Symphony Dynamo into its financial statements in the second quarter of 2006. To the extent that Dynavax contributes existing internal resources to the Symphony Dynamo programs as planned, the company currently estimates that the transaction may have a positive impact on both Dynavax's use of cash and the timing of future capital requirements.

Symphony Dynamo will be governed by a board of directors, comprised of one Dynavax representative, Dino Dina, MD, two representatives from Symphony Capital Partners, Harri Taranto and Mark Kessel, and two independent directors, one of whom is Ann Arvin, MD, the Lucile Salter Packard Professor of Pediatrics, Associate Dean of Research, Professor of Microbiology & Immunology and Chief of Pediatric Infectious Diseases at Stanford University School of Medicine.

JMP Securities LLC served as advisor to Dynavax in this transaction.

Conference Call Today

MentionedLastChange
DVAX 5.56Up0.01dollars or (0.18%)

Dynavax will hold a conference call to discuss the Symphony Dynamo transaction today at 4:30 pm Eastern/1:30 pm Pacific. To access the live call, please dial 866.543.6403 (US) or 617.213.8896 (international), passcode 90694187. Interested parties may listen to the webcast live at http://www.dynavax.com by clicking on the "Events" tab under the heading, "Investors." The webcast is also being distributed over CCBN's Investor Distribution Network to both institutional and individual investors. Individual investors can listen to the call through CCBN's individual investor center at http://www.fulldisclosure.com or by visiting any of the investor sites in CCBN's Individual Investor Network. Institutional investors can access the call via CCBN's password-protected event management site, StreetEvents, at http://www.streetevents.com . A telephonic replay will be available through April 24, 2006 by dialing 888-286-8010, access code 67463566. International callers can dial 617-801-6888, access code 67463566.

About Symphony Capital Partners, LP

Symphony Capital is a New York-based private equity firm that invests in development stage biopharmaceutical programs. Symphony has the most experienced team for project-specific financings and has $315 million in private equity capital dedicated to invest exclusively in the type of collaboration undertaken with Dynavax. Symphony Capital Partners is the lead investor in Symphony Dynamo. Additional information about Symphony is available at www.symphonycapital.com .

About RRD International, LLC

RRD International, LLC (RRD) is an innovative product development company dedicated to supporting the global regulatory, preclinical and clinical needs of biotechnology, pharmaceutical and medical device companies. RRD provides comprehensive strategic planning and operational support from program inception to product approval including the design, management and execution of clinical trials. RRD's team of highly experienced drug and device developers has a substantial record of favorable FDA interactions and outcomes. Through its customized and flexible business approach, RRD offers a unique risk-sharing model, enabling its goals and interests to be aligned with a partner company's success. Additional information about RRD is available at www.rrdintl.com .

About Dynavax

Dynavax Technologies Corporation discovers, develops, and intends to commercialize innovative products to treat and prevent allergies, infectious diseases, and chronic inflammatory diseases using versatile, proprietary approaches that alter immune system responses in highly specific ways. Our clinical development programs are based on immunostimulatory sequences, or ISS, which are short DNA sequences that enhance the ability of the immune system to fight disease and control chronic inflammation. Dynavax's pipeline includes: TOLAMBA(TM), a ragweed allergy immunotherapeutic, that has completed a large-scale Phase 2/3 clinical trial, and is in a supportive clinical trial in ragweed allergic children; HEPLISAV(TM), a hepatitis B vaccine that is currently in a pivotal Phase 3 clinical trial; a cancer therapy currently in a Phase 2 clinical trial; and an asthma immunotherapeutic that has shown preliminary safety and pharmacologic activity in a Phase 2a clinical trial.

Dynavax cautions you that statements included in this press release that are not a description of historical facts are forward-looking statements, including without limitation all statements regarding the agreement with Symphony Capital Partners, LP and its investors to provide $50 million of committed capital to advance Dynavax's ISS-based cancer, hepatitis B and hepatitis C therapeutic programs through clinical development; expectations that this agreement will build value in Dynavax's pipeline, accelerate the advancement of promising, early-stage development programs, will be minimally dilutive, reduce risk and provide a return on investment to shareholders; statements related to plans to advance its clinical programs in ragweed allergy, hepatitis B, hepatitis C and cancer and the commercial opportunities for those programs. Words such as "believes," "anticipates," "plans," "expects," "intend," "will," "slated," "goal" and similar expressions are intended to identify forward-looking statements. The inclusion of forward-looking statements should not be regarded as a representation by Dynavax that any of its plans will be achieved. Actual results may differ materially from those set forth in this release due to the risks and uncertainties inherent in Dynavax's business including, without limitation, risks relating to: plans to advance its cancer, hepatitis B and hepatitis C programs into clinical development and the therapeutic and commercial potential of these programs; and other risks detailed in the "Risk Factors" section of Dynavax's Annual Report on Form 10-K filed on March 16, 2006. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement and Dynavax undertakes no obligation to revise or update this news release to reflect events or circumstances after the date hereof.

SOURCE  Dynavax Technologies Corporation    -0-                             04/19/2006    /CONTACT:  Jane M. Green, PhD, Vice President, Corporate Communications ofDynavax Technologies Corporation, +1-510-665-4630, orjgreen@dvax.com/    /Web site:http://www.rrdintl.com//Web site:http://www.symphonycapital.com//Web site:http://www.dynavax.com/(DVAX)CO:  Dynavax Technologies Corporation; Symphony Capital Partners, LP;     RRD International, LLCST:  CaliforniaIN:  MTC HEASU:  FNCJA-HD-- SFW105 --2198 04/19/2006 16:00 EDThttp://www.prnewswire.com
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14.05.06 03:50 #32 imclone und elan kräftig ins Plus am Fr.
MCLONE SYSTEMS INC - Nasdaq National Market: IMCL (NEW charting help)

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 IMCL - ImClone Systems Inc (NASDAQ NM)5/12/2006 
 
01.06.06 17:17 #33 Elan, ELN der Highflyer
ELN - Elan Corporation, plc (NYSE)10:55 AM ET, 6/1/2006 

 

kein Kurseinbruch!

 
13.07.06 15:20 #34 wo geht es mit vertex hin???? o. T.
 
29.10.06 02:18 #35 @ stumpfpft sieht gut aus mit Vertex
godd news und good chance for Chart.
New Data for Investigational Hepatitis C Drug Telaprevir (VX-950) to be Presented at AASLD Meeting - Combination therapy with telaprevir and pegylated interferon suppressed both wild-type and resistant HCV -

BOSTON, Oct 27, 2006 /PRNewswire-FirstCall via COMTEX/ -- Researchers will
present new data this week suggesting that both wild-type hepatitis C virus and
resistant variants were suppressed in patients when pegylated interferon
(peginterferon alfa-2a; peg-IFN) was added to telaprevir (VX-950), Vertex's
investigational hepatitis C virus (HCV) protease inhibitor, in a Phase 1b
clinical study. In addition, clinical investigators will report that 24 of 26
patients who received telaprevir (VX-950) in two early-stage clinical trials had
undetectable HCV RNA after receiving follow-on combination therapy with peg-IFN
and ribavirin (RBV) through 24 weeks of treatment, a therapeutic regimen
following the conclusion of the clinical trials. Clinical investigators will
also report that some of these patients have stopped therapy, and that a
proportion of them continued to have undetectable HCV RNA after stopping
therapy.

The data will be presented while attending the 57th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD) and were released in accordance with media guidelines established by the conference. Telaprevir (VX-950) is an investigational drug candidate being developed as part of a global Phase 2b clinical development program by Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) Combination of Telaprevir (VX-950) and Peg-IFN Suppressed Both Wild-type Virus and Resistance Variants in 14-day Clinical Study

Tara Kieffer, Ph.D., of Vertex will present data in a Presidential Plenary session on Monday, October 30, analyzing viral sequences isolated from patients receiving telaprevir (VX-950) as a single agent or in combination with peg-IFN in a Phase 1b 14-day clinical study. In this study, viral variants were suppressed when peg-IFN was combined with telaprevir, or when peg-IFN and RBV were administered subsequent to telaprevir dosing.

In one arm of the trial, resistant viral variants were isolated from six of eight patients who had detectable HCV RNA while receiving telaprevir as a single agent over a period of 14 days. Subsequently, clinical investigators reported that all patients who received follow-on therapy with peg-IFN and RBV had undetectable HCV RNA at 24 weeks. In a second arm of the study, resistant viral variants were isolated from two of eight patients who received a combination of telaprevir and peg-IFN for 14 days. Both patients subsequently had undetectable HCV RNA at week 12 of follow-on therapy.

Current Status of Patients Receiving Follow-On Peg-IFN and RBV Combination Therapy After a 14-day, Phase 1b Clinical Trial of Telaprevir (VX-950)

On Tuesday, October 31, Dr. Nicole Forestier of Saarland University Hospital in Homburg, Germany will review the current status of 20 patients from a Phase 1b study who received 14 days of telaprevir therapy either alone or in combination with peg-IFN, or peg-IFN alone, in a poster presentation titled "Current status of subjects receiving peg-interferon alfa-2a (peg-IFN) and ribavirin (RBV) after a 14-day study of the hepatitis C protease inhibitor telaprevir (VX-950), with peg-IFN." Clinical investigators previously reported that at the end of 14 days of dosing, one of eight patients receiving telaprevir as a single agent and four of eight patients receiving telaprevir in combination with peg-IFN had undetectable HCV RNA (less than 10 IU/mL, Roche Taqman(R)).

All patients who did not discontinue therapy at week 24 are expected to continue to receive peg-IFN+RBV for a total of 48 weeks of treatment. The current status of patients, as reported by the poster authors, is described in the following table:

HCV RNA results for patients receiving follow-on peg-IFN+RBV therapy following

14-day Phase 1b study of telaprevir (VX-950)

Initial Patients Patients Patients Patients who Patients

14-day with with with stopped continuing

regimen undetectable undetectable undetectable therapy at to receive

(number HCV RNA at HCV RNA at HCV RNA at week 24 who peg-

of end of 14 end of 12 end of 24 had IFN+RBV

patients) days of weeks of weeks of undetectable through 48

dosing follow-on follow-on HCV RNA 12 weeks of

treatment treatment weeks post- follow-on

 
29.10.06 02:20 #36 Gute Zahlen bei Vertex
VERTEX PHARMACEUTICALS - Nasdaq National Market: VRTX (NEW charting help)

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 VRTX - Vertex Pharmaceuticals Inc (NASDAQ GS)10/27/2006 
 
29.10.06 02:25 #37 Einsteigen bei Medimmune

Charttechnisch buy und ein Mittel zur Vogelgrippe:

.S. Equity News: MedImmune's FluMist Sales Jump and CV Therapeutics Announces Presentations at American Heart Association Scientific Sessions 2006

Oct 27, 2006 (M2 PRESSWIRE via COMTEX) -- City of Industry, CA - Biotechnologyindustry alert provided by Equity IR News. MedImmune (Nasdaq: MEDI) is ready forflu season, and says sales of its FluMist flu vaccine helped boost revenue lastquarter. The Gaithersburg-based company had third-quarter revenue of $177million, up 15 percent from the same quarter a year ago. It reports a net lossof $55.8 million, or 23 cents per share, compared to a net loss of $64.1million, or 26 cents per share in the same quarter a year ago. U.S. BioDefense,Inc. (OTC BB: UBDE) subsidiary Emergency Disaster Systems (EDS) launches its newe-commerce site www.EDisasterSystems.com to expand its services and products andincrease its accessibility to current corporate clients and its retail customerbase. For the last ten years EDS has focused primarily on providing itscorporate clients like Toyota and Kaiser with innovative emergency preparednesstechnology.

CV Therapeutics, Inc. (Nasdaq: CVTX) announced that data from threeranolazine-related studies will be presented at the American Heart Association(AHA) Scientific Sessions 2006, which will be held at McCormick Place inChicago, IL, on November 12 - 15, 2006. CV Therapeutics, Inc., headquartered inPalo Alto, California, is a biopharmaceutical company focused on applyingmolecular cardiology to the discovery, development and commercialization ofnovel, small molecule drugs for the treatment of cardiovascular diseases.Celgene Corporation (Nasdaq: CELG) announced adjusted net income of $59.4million, or adjusted earnings per diluted share of $0.15 for the quarter endedSeptember 30, 2006. Based on U.S. Generally Accepted Accounting Principles(GAAP), Celgene reported net income of $20.4 million, or diluted earnings pershare of $0.05 for the quarter ended September 30, 2006, including share-basedemployee compensation expense, compared to net income in the prior year periodof $0.7 million.

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MEDIMMUNE INC - Nasdaq National Market: MEDI (NEW charting help)

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 MEDI - MedImmune Inc (NASDAQ GS)10/27/2006 

 
16.12.06 09:27 #38 Shire Plc aus England
 SHPGY - Shire Plc (NASDAQ GS)12/15/2006 
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21.01.07 20:38 #39 Friedman,Billings,Ramsey &Co - Alkermes outpe.
Friedman,Billings,Ramsey &Co - Alkermes "outperform"  

07:56 19.01.07  

Rating-Update:

Arlington (aktiencheck.de AG) - Die Analysten von Friedman, Billings, Ramsey & Co stufen die Aktie von Alkermes (ISIN US01642T1088/ WKN 882907) unverändert mit "outperform" ein. Das Kursziel werde bei 22 USD gesehen. (19.01.2007/ac/a/u)



Quelle: aktiencheck.de
 
21.05.07 15:16 #40 Elan dreht heute ab, in 2 Wochen 30%
http://www.rt.boerse-stuttgart.de/pages/details/...RX.STU&ChartHist=1

2nd UPDATE: Elan Up On Early Phase III For Alzheimer's Drug5-21-07 7:15 AM EDT

By Quentin Fottrell
Of DOW JONES NEWSWIRES

DUBLIN -(Dow Jones)- Shares in Elan Corp. PLC (ELN) surged Monday after the Irish drug group and U.S. partner Wyeth (WYE) said they will start early Phase III clinical trials of AAB-001, their treatment for mild to moderate Alzheimer's disease which analysts say could become a blockbuster drug.

With Phase III starting in mid-2007 rather than mid-2008 as previously expected, analysts say AAB-001 could potentially receive approval by the U.S. Food & Drug Administration by late-2008.

Investors liked the news, which indicates increased confidence in the Alzheimer's program. At 1050 GMT, Elan shares reached a daily high, rising nearly 13%, or EUR1.50, at EUR13.20 in Dublin, out performing the broader market with the ISEQ Overall Index up 0.9% at 9751. Although Phase II is not yet complete, the two drug companies said Phase III clinical trial design will be finalized with regulatory agencies, and subject to their approval, it will begin in the second half of 2007.

Davy Stockbrokers, which doesn't rate shares, raised its sum-of-the-parts valuation for Elan to $21.00 from $16.10 to reflect the "advance" in the Alzheimer's program. "This is a key catalyst for the shares," Davy's Jack Gorman said.

NCB Stockbrokers' Orla Hartford, who rates Elan a buy, said there was "real potential" for early filing of AAB-001, adding that interim analysis of Phase II over the next three months could "transform Elan's investment case."

She said that evidence of plaque reduction on the brain by AAB-001 with statistical evidence on quality of life improvements would provide a "compelling case" for filing AAB-001 for approval after Phase II is completed.

Goodbody Stockbrokers' Ian Hunter welcomed the early Phase III, but added, " The only frustrating element for the market is that, given that the Phase II trial is ongoing, we will not get a sight of the data until early 2008."

Hunter maintains a buy recommendation on Elan, predicting "conservative" peak annual sales for AAB-001 of $2.2 billion by 2014 should the treatment get final approval by the regulatory authorities.

"The Alzheimer's market is huge," Hunter said. "It has the potential to be the next big indication for pharmaceutical companies, especially as the baby boomers come into the Alzheimer's-prone age group."

Last month, Elan Corp's chief executive officer Kelly Martin told Dow Jones Newswires that there are about 10 million Alzheimer's patients in the U.S. and Europe, with tens of billions of dollars of potential revenue.

He also flagged a "series of Alzheimer's advancements" by year-end, shifting the focus away from Elan's multiple sclerosis drug Tysabri, which has up until now been the main focus for investors in the company.

Elan's share price has had a rollercoaster ride over the last five years: falling from its 2002 high of EUR50.27 due to revelation of now-resolved accounting troubles in 2002, and the temporary suspension of Tysabri in 2005.

In February 2005, Elan and joint venture partner Biogen Idec PLC (BIIB) suspended Tysabri in the U.S. on safety grounds. Tysabri was re-launched in the U.S. and launched for the first time in the E.U. in June 2006.

That temporary setback followed a long and arduous recovery for Elan, beginning with a change of senior management in 2002 when its former CEO and Chairman, the late Donal Geaney, resigned amid accounting troubles.

Company website: http://www.elan.com

-By Quentin Fottrell, Dow Jones Newswires; +353-1-6762189; quentin.fottrell@ dowjones.com

 (END) Dow Jones Newswires
 05-21-070715ET
 Copyright (c) 2007 Dow Jones & Company, Inc.



________
Alles was ich hier poste, ist eine Satire.
Nichts ist wahr, Alles ist nur eine Geschichte.
Ähnlichkeit mit lebenden oder verstorbenen Personen sind rein zufällig.
Ähnlichkeit mit Tatsachen sind reiner Zufall.
Charts oder andere Meinungen sind keine Kaufempfehlungen.
Alles was ich hier schreibe sind reine Fiktionen.
Ein Bezug aus dieser virtuellen Welt zur realen Welt ist rein zufällig, nie intendiert und unterliegt der Täuschung des Lesers.  
01.08.08 13:48 #41 Kaufempfehlung ELAN CORP.
02.08.08 11:54 #42 krass
 

Bewertung:
2

04.08.08 19:16 #43 PLUS 15,7 % today
 

Bewertung:
1

24.01.11 14:32 #44 hier

hat sich ja seit jahren nichts mehr getan. sollte sich das ändern? na ja, am pusch solls nicht hapern. schaun wer mal. es grüßt mcgeiz

 
26.04.11 17:14 #45 hallo mckragen
nun tut sich eine ganze menge, am 28.4. entscheidet sich ob ein weiters medikament
in die produktion gehen darf, darum die anstiege.
Kursziele werden mit etwa 50€ prognostiziert.  
26.04.11 17:20 #46 Finde Vakzine (ähnlich DNDN) vielversprechend
NWBO.OB, BVTI.PK + ABPI.PK, IMUC.OB  
10.05.11 19:22 #47 23.5.2011

am 23.5 ist es soweit.., die Us Gesundheitsbehörde beschließt ob das Medikament (telaprevir) auf den Markt darf oder nicht...hoffe mal alles geht gut und der kurs steigt weiter

 
13.11.11 12:32 #48 wiesogeht viropharma so ab
haben die ein neues Medikament?  
02.05.14 15:40 #49 Gefährlich..
Fokussiert man die Zahlen von Alkermes, geht es seit mehreren Quartalen nur bergab.
Die Anleger scheinen aktuell aber auf eine gute Zukunft zu hoffen.


http://www.erfolgreichinvestieren.ch/wp/...kermes-aktie-kein-hit-ist/  
29.06.18 10:51 #51 Health Canada genehmigt PrSYMDEKO
Health Canada Approves PrSYMDEKO™ (tezacaftor/ivacaftor and ivacaftor) to Treat the Underlying Cause of Cystic Fibrosis in People Ages 12 and Older with Certain Mutations in the CFTR Gene

-SYMDEKO is Vertex’s third medicine to treat the underlying cause of CF-

-Approximately 2,000 people in Canada are ages 12 and older and have two copies of the F508del mutation or at least one mutation in the CF gene that is responsive to treatment with SYMDEKO-

https://www.businesswire.com/news/home/...orivacaftor-ivacaftor-Treat  

Bewertung:
1

24.10.18 17:35 #52 ALKS 41,80$
1. November FDA Panel  
02.11.18 12:46 #54 klares negatives Panel 2-21
  • Did Alkermes present substantial evidence of the drug’s efficacy? (20 no / 3 yes)
  • The researchers had adequately characterized the safety of the drug? (13 yes / 10 no)
  • Support a favorable benefit/risk profile? (21 no / 2 yes)

Nachbörslich ging es 9% runter.

https://endpts.com/...s-5461-slamming-the-company-on-multiple-fronts/


 
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