Celldex Therapeutics garantierte 100 % bis 06/10
Celldex erhält dafür erstmal 50 Millionen USD.
MA (50) bei 5.33 USD zieht bald durch den MA(200) dann sage ich ein Feuerwerk vorraus,
rechne da mit nem deutlichen Volumenspike (an die 2 Millionen Shares sind drin) der Kurs wird dann ruck zuck an die 8 USD gehen
Celldex läuft gut, Kerx läuft Celldex aber den Rang ab, owbwohl die Pipeline Celldex wesentlich voller ist
#1095: Correlation of GPNMB expression with outcome in breast cancer (BC) patients treated with the antibody-drug conjugate (ADC), CDX-011 (CR011-vcMMAE).
Saturday, June 5
2:00 PM - 6:00 PM
Speaker: Mansoor N. Saleh
CDX-011: Melanoma
#8525: Frequent dosing and GPNMB expression with CDX-011 (CR011-vcMMAE), an antibody-drug conjugate (ADC), in patients with advanced melanoma.
Monday, June 7
8:00 AM - 12:00 PM
Speaker: Omid Hamid
CDX-110: Brain Cancer
#2014: Interim data for ACT III: Phase II trial of PF-04948568 (CDX-110) in combination with temozolomide (TMZ) in patients (pts) with glioblastoma (GBM).
Saturday, June 5
8:00 AM - 12:00 PM
Speaker: Rose Lai
CDX-1307: Bladder Cancer
#TPS228: A randomized phase II study of a novel antigen-presenting cell-targeted hCG-β vaccine (the CDX-1307 regimen) in muscle-invasive bladder cancer.
Monday, June 7
8:00 AM - 12:00 PM
Speaker: Deborah Ann Bradley, MD
volume much higher than last year
last year we had an average of about 50.000 (3x 50.000) would be 150.000 for 35 million shares
2010 there is a volume of around 500.000 (average) 3-4 times more than 2009!!!
Ich verfolge deine Postings auch in anderen Threads mit großen Interesse. Sehr viel Sachverstand gepaart mit Herzblut. Toll. Vielen Dank.
Am 21.April präsentiert Celldex Daten (vorklinisch) zu CDX 1127, sind diese gut, könnte das sich ein wenig kurstreibend auswirken. Viel entscheidender sind natürlich jedoch die Daten im Juni. Der 1.Mai kommt näher und daher auch die so wichtige Zulassung des Wirkstoffs Provenge von Dendreon. Celldex schloss am Freitag bei 7.03 USD überraschend gut, wie ich finde...jeder Dip wir zum Kauf/Nachkauf genutzt.
Upcoming Events
Celldex Therapeutics to present Poster on CDX-1127 Preclinical Results at the American Association for Cancer Research (AACR) 101st Annual Meeting 2010
Wednesday, April 21, 2010 8:00 a.m. ET
Description§Supporting Materials to follow subsequent to Poster Session
Location§Washington, DC
so jetzt bin ich auch mit 1000 Stück dabei, Celldex ist eine sehr interessante Firma und sollte Dendreon die erhoffte Zulassung erhalten, kommt sicher auch hier ein gehöriger Schub in die Aktie!
Denke die 16 USD könnten im Juni drin sein, über 10 USD gehts auf jedenfall während der ASCO.
Langfristig ist hier aber ordentlich mehr Potential vorhanden. (wegen CDX 011 und vorallem CDX 1307)
Neuer Antibody mit positiven Ergebnissen:
http://finance.yahoo.com/news/...-for-bw-3594601269.html?x=0&.v=1
Dann wünsch ich uns mal viel Erfolg!
vom Wortlaut her klingt das nach dir "It's too early to tell if Celldex is the next Dendreon"
http://www.thestreet.com/story/10732313/5/...k-mailbag-labopharm.html
http://investing.businessweek.com/research/stocks/...p?ticker=CLDX:US
für eine neue Medizin...
"Additionally, if Provenge is finally granted approval, then it could lead to a nice rally in the cancer immunotherapy sector as a whole."
aber hallo denke Celldex wird die 8 USD brechen..
http://seekingalpha.com/article/...-likely-to-be-approved-in-mid-2010
Dendreon erhält die Zulassung für Provenge...
bei Celldex hat sich jemand gestern einen rießigen Block geleistet...und ich war das sicherlich nicht
für mich ist Celldex immer noch viel zu billig, Regeneron hat noch keinen Antibody auf dem Markt und wird mit 2 Milliarden bewertet, lächerlich (Celldex ist jetzt bei 250 Millionen, bei 70 Millionen im Cashbestand)
http://www.thestreet.com/story/10741201/5/...tocks-with-new-data.html
rechne weiterhin mit 16 USD im Juni
Premarket gehts weiter rauf, aber auch bei Kerx, Dndn und Co
NEW YORK ( Dow Jones )--The Food and Drug Administration approval of Dendreon Corp.'s (DNDN) new prostate cancer therapy offers hope to patients. It could also help developers of similar drugs. On Thursday, the FDA approved Provenge, the first of a new class of cancer therapies that work by stimulating the immune system to attack the disease. Seattle-based Dendreon had been trying to get approval for Provenge since late 2006, but was asked to find more data. The approval of Provenge is a dramatic development in the fight against cancer and could pave the way for a host of similar therapies. Other companies, including Celldex Therapeutics Inc. (CLDX) and GlaxoSmithKline PLC (GSK, GSK.LN), are developing products that work the same way. Provenge's approval suggests those products could make it to the market, potentially stimulating new interest from pharmaceutical companies and venture capitalists. "It sets the stage, or at least facilitates, the approval of other cancer vaccines," said Michael Becker, chief executive of MD Becker Partners, a management consulting and strategic advisory firm for life science companies. "It is a watershed event in that regard." The approval of Provenge is similar to the 1997 approval of Rituxan. That therapy was the first monoclonal antibody to reach the market and ushered in a new era for biologic drugs. Within five years, five more monoclonal antibodies were approved in the U.S., a pattern that Becker predicts will be repeated with cancer vaccines. Robert Baird & Co. analyst Christopher Raymond believes Provenge will improve investor perception of the entire biotech industry, which has suffered from funding problems and lackluster initial public offerings. Financing re-emerged for biotechnology companies after successful data about Avastin, another cancer therapy, emerged in 2003, he said. Plenty of companies could benefit from renewed interest in cancer vaccines. Among them: Celldex, which is developing a brain cancer vaccine with Pfizer Inc. (PFE), and Geron Corp. (GERN), which has a midstage vaccine for acute myelogenous leukemia. GlaxoSmithKline has a vaccine for lung and skin cancers in late-stage trials. Other companies involved in the space include Bristol-Myers Squibb Co. (BMY), Vical Inc. (VICL) and Biovest International Inc. (BVTI). Still, an improved image for cancer vaccines won't be enough. These companies need to prove their drugs work and get them cleared by the FDA, which can be rigorous for any therapeutic class. Concept Capital's Washington Research Group said the Provenge approval demonstrates what's needed by the FDA. But it notes that different drugs may have a harder time than others, and the agency will continue to review drugs in a "case specific nature." While Provenge is personalized for each patient, Becker notes that only 27% of cancer vaccines in development at both public and private companies use a similar method. The rest are "off the shelf," meaning that they are the same for everyone, but still aim to stimulate the immune system. Provenge provides proof that the method works, but the future will be in off-the-shelf treatments that will be easier to make and have a lower price tag, Becker said. -By Thomas Gryta, Dow Jones Newswires; 212-416-2169; thomas.gryta@ dowjones .com
For the full year, analysts expect the company to post a loss of $1.15. In the year-ago period, the company reported a loss of $0.53 on sales of $4 million.
In the previous quarter, the company reported a loss of $0.28, topping consensus estimates for a loss of $0.29.