Das könnte abgehen....

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eröffnet am: 30.01.09 11:58 von: Touwse Anzahl Beiträge: 1095
neuester Beitrag: 16.10.15 02:19 von: Heron Leser gesamt: 89106
davon Heute: 2
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30.01.09 11:58

3 Postings, 3980 Tage TouwseDas könnte abgehen....

La Jolla könnte durchaus noch raketenartig abgehen.

Die beiden ersten Stufen waren erfolgreich, und das Ergebnis der finalen Stufe III soll im 1. Quartal 2009 vorliegen.

Die Kursentwicklung der letzten Tage scheint dem Rechnung getragen zu haben.

Ich glaube, dass ist eine Beobachtung hier lohnenswert ist. Was meint ihr dazu ?

Moderator: neemax
Zeitpunkt: 30.01.09 13:00
Aktion: Forumswechsel
Kommentar: Falsches Forum



21.04.09 19:52

5662 Postings, 4406 Tage _bbb_hm...

27.05.09 17:55

4951 Postings, 4390 Tage 0815axKERX - Goden Cross MA(50) -- MA(200)

Angehängte Grafik:
kerx.png (verkleinert auf 65%) vergrößern

27.05.09 17:59

4951 Postings, 4390 Tage 0815axMeeting of the American Society of Clinical...

Keryx Biopharmaceuticals Announces Poster Presentations Highlighting Clinical Activity of KRX-0401 (Perifosine) at the Upcoming Annual Meeting of the American Society of Clinical Oncology

   * On Monday May 18, 2009, 8:29 am EDT

Results Will be Reported from Phase 2 Studies Evaluating KRX-0401 in Advanced Renal Cell Carcinoma, Colorectal Cancer and Gastrointestinal Stromal Tumors (GIST)

NEW YORK, May 18 /PRNewswire-FirstCall/ -- Keryx Biopharmaceuticals, Inc. (Nasdaq: KERX - News) today announced that four abstracts on KRX-0401 (Perifosine), the Company's Akt-inhibitor for cancer, were accepted for presentation during poster sessions taking place at the 45th Annual Meeting of the American Society of Clinical Oncology (ASCO), to be held in Orlando, Florida from May 29 to June 2.

All of the clinical data to be presented demonstrates the potential clinical efficacy of KRX-0401, both as a single agent and in combination with other approved agents, in the treatment of patients with advanced renal cell carcinoma, colorectal cancer and GIST.

...(weiter siehe LINK)

27.05.09 18:37

4149 Postings, 5330 Tage martin30smWas ist denn da los?

Wow, die geht ja ordentlich UP!  

27.05.09 19:42

4951 Postings, 4390 Tage 0815axmartin...: Insider-Käufe, Studien-Resultate...

Angehängte Grafik:
kerx.png (verkleinert auf 72%) vergrößern

28.05.09 15:37

4951 Postings, 4390 Tage 0815ax...

der gestrige Tag im Chart:
Angehängte Grafik:

28.05.09 16:27

4149 Postings, 5330 Tage martin30smBin gestern zu 0,67 Dollar raus!

Okay, 40% Gewinn waren es auch!  

28.05.09 16:36

4951 Postings, 4390 Tage 0815axGlückwunsch @ martin...

- ich halte meine Position noch (Einstieg 0,42 USD)

29.05.09 15:31

4951 Postings, 4390 Tage 0815ax..

Angehängte Grafik:

30.05.09 07:35

4951 Postings, 4390 Tage 0815axKERX Reports Single Agent Phase 2 Data of KRX-0401

Keryx Biopharmaceuticals Reports Single Agent Phase 2 Data of KRX-0401 (Perifosine) Further Demonstrating KRX-0401's Activity in the Treatment of Advanced Metastatic Renal Cell Cancer

* On Friday May 29, 2009, 4:30 pm EDT


KERK 29.05.2009 16:00 $0.70

KERX 29.05.2009 19:59 $1.01

( )

30.11.09 16:26

2596 Postings, 3986 Tage kalle50Diejenigen unter euch

die vorzeitig das Handtuch geworfen haben dürften sich mittlerweile schwarzärgern da Keryx mittlerweile die 3 USD im Visier hat, jetzt stellt euch mal vor wen die Firma eventuell mal von einem der großen geschluckt wird wo der Kurs dann hingeht.  

30.11.09 17:08

4951 Postings, 4390 Tage 0815ax...halte noch immer meine

1500 Stk. @ 0,3?

(hätte ich zum damaligen Zeitpunkt mehr Geld "flüssig" gehabt, wären nun noch mehr im Depot eingebucht...)
*amM - keine Kaufempfehlung

02.12.09 17:42

4951 Postings, 4390 Tage 0815axKeryx Receives FDA Fast Track Designation ...

02.12.2009 14:36

Keryx Receives FDA Fast Track Designation for KRX-0401 (Perifosine) for the Treatment of Relapsed/Refractory Multiple Myeloma

NEW YORK, Dec. 2 /PRNewswire-FirstCall/ -- Keryx Biopharmaceuticals, Inc. today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for KRX-0401 (perifosine), the Company's novel, potentially first-in-class, oral anti-cancer agent that inhibits the phosphoinositide 3-kinase (PI3K)/Akt pathway, for the treatment of relapsed/refractory multiple myeloma.

The Fast Track program of the FDA is designed to facilitate the development and expedite the review of new drugs that are intended to treat serious or life-threatening conditions and that demonstrate the potential to address unmet medical needs. Fast Track designated drugs ordinarily qualify for priority review, thereby expediting the FDA review process.

A Phase 3 trial investigating perifosine in combination with bortezomib (VELCADE®) and dexamethasone for the treatment of patients with relapsed/refractory multiple myeloma is expected to commence by year-end under a Special Protocol Assessment (SPA) with the FDA. In addition, in September, the Company announced that perifosine had received Orphan-Drug designation in the United States for the treatment of multiple myeloma.

Ron Bentsur, Chief Executive Officer of Keryx Biopharmaceuticals, commented, "This Fast Track designation can significantly reduce the FDA review time of a new drug application, and therefore can expedite the time to market for perifosine in multiple myeloma." Mr. Bentsur added, "We believe that the Fast Track designation, together with the SPA and Orphan Drug status previously granted to us by the FDA for perifosine in multiple myeloma, significantly enhances the value proposition of perifosine in this indication. We are eager to begin the Phase 3 trial later this month."

KRX-0401 (perifosine) is in-licensed by Keryx from Aeterna Zentaris, Inc. (Nasdaq: AEZS; TSX: AEZ) in the United States, Canada and Mexico.

(...weiter siehe LINK)
*amM - keine Kaufempfehlung

05.12.09 18:36

2596 Postings, 3986 Tage kalle50Hallo Touwse!

Oder irgendjemand  anderes??? Wofür bekommt man dieses Kreuz ist es eventuell die Laune irgendwelcher Teilnehmer,Habe in dem Marenica Thread auch ein Bekommen und bin mir keiner Schuld Bewußt????  

07.12.09 17:22

21642 Postings, 4040 Tage HeronNews

Keryx Biopharmaceuticals, Inc. Reports Aktualisiert Phase 1 / 2 Daten, einschließlich der neuen Survival-Daten, auf KRX-0401 (Perifosine) in der Behandlung von fortgeschrittenem Multiplen Myelom auf der 51. Jahrestagung der American Society of Hematology  

17.12.09 11:24

21642 Postings, 4040 Tage Heronstartet Phase 3 Zulassungsstudie der KRX-0401

Keryx Biopharmaceuticals, Inc. startet Phase 3 Zulassungsstudie der KRX-0401 (Perifosine) zur Behandlung von Patienten mit fortgeschrittenem Multiplen Myelom

... (automatisch gekürzt) ...
Moderator: lassmichrein
Zeitpunkt: 03.02.10 17:16
Aktion: Kürzung des Beitrages
Kommentar: Urheberrechtsverletzung, bitte nur zitieren



08.01.10 21:56

4951 Postings, 4390 Tage 0815axi

*amM - keine Kaufempfehlung

15.01.10 22:25

4951 Postings, 4390 Tage 0815axHealthcare Conference Updates: KERX

Healthcare Conference Updates: KERX
Written by Mike Havrilla      
Friday, 15 January 2010 09:09
Below are some updates and developments from the past week, which I spent in San Francisco for the OneMed, JP Morgan, and other healthcare conferences.
I had the opportunity to meet with the CEO (Ron Bentsur) and CFO (James Oliviero) of Keryx Biopharma (NASDAQ: KERX) on Wednesday and was impressed with the Company's focused strategy and upcoming milestones for 2010 and beyond. As outlined in my overview article last week, I have purchased shares of KERX over the past week on weakness at a slightly higher price range ($2.70-2.75) than I originally projected.
Given the Company's history of in-licensing compounds for development and robust cash position, I inquired if anything was on the horizon in this regard. However, for the near to intermediate term, Keryx plans to remain focused on utilizing its resources (cash / personnel) to get the Phase 3 trials well established before considering any new acquisitions, which is a good strategy given that Keryx is well-funded but still a small-cap drug developer that needs to remain focused.
Approximately $10-11 million is the estimated cost to fund both the short and long-term Phase 3 studies of Zerenex while perifosine has estimated funding of $12 million each to fund the Phase 3 studies for multiple myeloma (ongoing) and colorectal cancer (pending), with an estimate of $25,000-$30,000 per patient to fund the Phase 3 cancer trials. Below is a summary of additional details for upcoming catalysts and milestones for Keryx over this year and beyond that were not included in my overview article last week.
During 2010, Keryx expects to report updated data from its Phase 2 colon cancer study, conduct / update additional earlier stage Phase I/II studies, finalize late-stage trial protocol for colon cancer study, and begin additional late-stage studies for colon cancer in addition to the pending pivotal Phase 3 study of perifosine under a SPA agreement with FDA for multiple myeloma. KERX expects to provide an update on Phase 2 colon cancer survival and other data for perifosine next weekend at GI-ASCO 2010 (Jan. 22-24) as it prepares to begin a pivotal Phase 3 trial of perifosine in colon cancer patients with a Special Protocol Assessment (SPA) with the FDA possible for this indication within the next 2-3 months (i.e. mid-April 2010).  
The ongoing Zerenex Phase 2 study in Japan by JT Torii is near completion and Keryx expects the Phase 3 trial to begin during 2H10, which will trigger a development milestone payment that is in the mid single-digit million dollar range. An additional $15 million milestone is possible upon regulatory approval in Japan, with approximately $55 million in remaining milestone payments based on the achievement of sales targets upon commercialization.
Zerenex represents a niche market opportunity within well understood / established class of drugs (phosphate binders) that has a key differentiation of being iron-based compared to existing treatments such as PhosLo, Fosrenol, and Renagel/Renvela. Zerenex is expected to offer an improved safety profile / patient acceptance with reduced GI / bloating side effects and approximately 50% less dosing burden (i.e. taking less pills less often) compared to existing phosphate binders.
In addition, a major secondary endpoint being evaluated is the potential ability of Zerenex to decrease the need for IV-iron and blood cell stimulators (EPO agents such as Epogen and Aranesp) since it is iron based and expected to result in long-term accumulation of the mineral. This may result in a first-line phosphate binder indication (with a goal of capturing 20-25% market share) for Zerenex and advantages that include safety (there is a pending FDA Advisory Panel to discuss safety issues of EPO drugs) and economic (dialysis bundling payment issues - Zerenx has potential to save dialysis providers money by reducing need for IV-iron or EPO agents).

*amM - keine Kaufempfehlung

22.01.10 17:17

21642 Postings, 4040 Tage HeronNews

Aktualisiert Ergebnisse aus Phase 2 Clinical Trial of KRX-0401 in Kombination mit Capecitabin zur Behandlung von metastasiertem Darmkrebs-am Sonntag, 24. Januar 2010 Präsentiert werden  

22.01.10 18:08

618 Postings, 3557 Tage iBrokerEmpfehlung DerAktionär

DerAktionär empfiehlt die Aktie im aktuellen Spezialreport -> Kursziel EUR 3,50  

25.01.10 14:46

4951 Postings, 4390 Tage 0815axKeryx Reports Statistically Significant Benefit ..

Keryx Reports Statistically Significant Benefit in Survival from Updated Results of a Randomized, Double-Blind, Placebo-Controlled Phase 2 Study of KRX-0401 (Perifosine) in the Treatment of Advanced Metastatic Colon Cancer
Data Reported at the 2010 ASCO GI Cancers Symposium Demonstrate a Statistically Significant Improvement in Both Time to Tumor Progression and Overall Survival in the Perifosine + Capecitabine Arm Versus Placebo + Capecitabine Arm
Conference Call to Discuss Data to be Held on Thursday, January 28th at 9am EST  
Monday January 25, 2010, 8:30 am


*amM - keine Kaufempfehlung
*amM - keine Kaufempfehlung

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