Cytrx corp.WKN: 879214 - 15% sind möglich!

CytRx Scientific Advisory Board Member Dr. Craig C. Mello Awarded Nobel Prize in Medicine for RNAi Discovery

Tuesday October 3, 8:51 am ET

LOS ANGELES--(BUSINESS WIRE)--CytRx Corporation (Nasdaq:CYTR - News) today applauded the announcement that its Scientific Advisory Board member Craig C. Mello, Ph.D., together with Andrew Fire, Ph.D., was awarded the Nobel Prize in medicine for discovery of the use of double-stranded RNA for gene silencing, a technology that has come to be known as RNA interference (RNAi). Drs. Mello and Fire acted as key inventors on the first approved RNAi patent, which is licensed to CytRx on a non-exclusive basis.
As a member of the CytRx Scientific Advisory Board, Dr. Mello acts in an advisory capacity to assist the Company to develop RNAi therapeutics for specific diseases.
Dr. Mello is the Blais University Chair and Distinguished Professor of Molecular Medicine and a Howard Hughes Medical Institute Investigator at the University of Massachusetts Medical School, in Worcester, Mass. In this capacity, Dr. Mello studies both the biochemical pathway responsible for RNAi and the regulation of gene expression. He has numerous publication credits including 16 in the prestigious journals Science, Nature, Cell, and the Proceedings of the National Academy of Sciences.
"We extend our sincerest congratulations to Drs. Mello and Fire for receiving this celebrated award and are delighted that the Nobel committee has recognized the potential of this highly novel approach that has implications over a broad range of catastrophic diseases," said President and CEO Steven A. Kriegsman. "RNAi could offer an entirely new paradigm in disease treatment by regulating the effect of specific diseases, making it a valuable tool in drug discovery, as well as a direct therapeutic. At CytRx, we are involved in drug discovery using RNAi targeting for major global health concerns that include obesity and type 2 diabetes."
CytRx uses RNAi to help screen and identify classical, orally-available small molecule drugs. In its obesity and type 2 diabetes programs, CytRx is using its proprietary high throughput RNAi-based screening technology to screen the more than 2,000 candidate genes that may be involved in diabetes and obesity in order to rapidly validate numerous drug targets in the most critical pathways which regulate metabolism. During the past year, CytRx-sponsored research programs have discovered and validated approximately 30 new type 2 diabetes and obesity drug targets. CytRx also is exploring the utility of RNAi for direct therapeutic applications when technically feasible.
"We strongly believe in the value of RNAi technology, which has prompted us to pursue a plan, subject to obtaining necessary funding, to transfer all of our RNAi therapeutics assets into a newly-formed subsidiary to accelerate the development and commercialization of drugs based on this platform," added Mr. Kriegsman. "We plan to continue using RNAi gene silencing technology as a drug discovery tool to facilitate our small molecule drug discovery program."
RNAi Background
RNA is a constituent of all living cells and many viruses, consisting of a long, usually single-stranded chain of alternating phosphate and ribose units with the bases adenine, guanine, cytosine, and uracil bonded to the ribose. The structure and base sequence of RNA is used by the cell as a messenger (mRNA) to be used as an "instruction manual" for the synthesis of a specific protein. RNAi technology uses short double-stranded RNA, or dsRNA, molecules to silence targeted genes and, as a result, is commonly referred to as "gene silencing." RNAi has been shown to effectively silence targeted genes within living cells with great specificity and potency. The end result is the destruction of the specific mRNA, thus silencing that gene and the protein that the mRNA would normally be used to synthesize.
About CytRx Corporation
CytRx Corporation is a biopharmaceutical research and development company engaged in the development of high-value human therapeutics. The Company owns three clinical-stage compounds based on its small molecule "molecular chaperone" co-induction technology. In September 2006, CytRx reported reaching the primary endpoints of safety and tolerability from a Phase IIa trial with its lead small molecule product candidate arimoclomol for the treatment for amyotrophic lateral sclerosis (ALS or Lou Gehrig's disease). Also in September 2006 CytRx announced receipt of $24.5 million in a non-dilutive agreement with the privately funded ALS Charitable Remainder Trust to fund continued arimoclomol development for the treatment for ALS in return for one percent royalty payment from potential worldwide sales of arimoclomol for the treatment of ALS to The Greater Los Angeles Chapter of The ALS Association. Arimoclomol has received Orphan Drug status and Fast Track designation from the U.S. Food and Drug Administration.
CytRx has previously announced that a novel polyvalent HIV DNA + protein vaccine exclusively licensed to CytRx, developed by researchers at the University of Massachusetts Medical School (UMMS) and Advanced BioScience Laboratories, and funded by the National Institutes of Health, demonstrated very promising interim Phase I clinical trial results that indicate its ability to produce potent antibody responses with neutralizing activity against multiple HIV viral strains. CytRx also has a broad-based strategic alliance with UMMS to develop novel compounds in the areas of ALS, obesity, type 2 diabetes and cytomegalovirus (CMV) using RNAi technology. The Company has a research program with Massachusetts General Hospital, Harvard University's teaching hospital, to use RNAi technology to develop a drug for the treatment of ALS. CytRx Drug Discovery division, located in Worcester, Mass., focuses on the use of RNAi technologies to develop small molecule and RNAi therapeutics to treat obesity and type 2 diabetes. For more information, visit CytRx's Web site at www.cytrx.com.
Forward-Looking Statements
This press release may contain forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended. Examples of such statements include, but are not limited to, statements relating to the expected timing, scope and results of our clinical development and research programs, including the initiation of clinical trials, and statements regarding the potential benefits of our drug candidates and potential drug candidates. Such statements involve risks and uncertainties that could cause actual events or results to differ materially from the events or results described in the forward-looking statements, including risks or uncertainties related to the early stage of CytRx's RNAi, diabetes, obesity, cytomegalovirus and ALS research, the need for future clinical testing of any RNAi-based product candidates and small molecules that may be developed by CytRx using RNAi screening methods, the significant time and expense that will be incurred in developing any of the potential commercial applications for CytRx's RNAi technology or small molecules, uncertainties related to regulatory approvals for clinical testing and the scope of the clinical testing that may be required by regulatory authorities for its molecular chaperone co-induction drug candidates, including arimoclomol, and other products, and the timing and outcomes of those tests, risks relating to the enforceability of any patents covering CytRx's products and to the possible infringement of third party patents by those products, and the impact of third party reimbursement policies on the use of and pricing for CytRx's products. Additional uncertainties and risks are described in CytRx's most recently filed SEC documents, such as its most recent annual report on Form 10-K, all quarterly reports on Form 10-Q and any current reports on Form 8-K filed since the date of the last Form 10-K. All forward-looking statements are based upon information available to CytRx on the date the statements are first published. CytRx undertakes no obligation to publicly update or revise any forward- looking statements, whether as a result of new information, future events or otherwise.

Contact:
CEOcast, Inc.
Kevin Theiss
ktheiss@ceocast.com
Cormac Glynn
cglynn@ceocast.com
212-732-4300

 

In NY ein Plus von über 26 % und ein Aktienumsatz von ca.12 Mio.Stück (Durschn. ca. 800 Tsd.). Toll, nur niemand weiß warum ! Es gibt keine News, keine Analystenkommentare oder FDA-Statements. Vielleicht sollte ich besser schreiben : Noch nicht und irgendjemand weiß hier bereits über Dinge Bescheid die wir erst nächste Woche erfahren.  

Die Aktie kostet schon Nerven. Gestern hat sie aber in NY mit einem Plus von über 21 % abgeschlossen. Die hoffungsvollen News verdichten sich, auch kommt wieder Fantasie rein. Vielleicht gelingt es doch noch vor Weihnachten die 2 Dollar wieder deutlich zu überwinden.  

Ein Plus von 35 % in dieser Woche. neuer 3 Jahrehöchststand. Gute Aussichten mit Geschäftsmodell. Die Aktie könnte einer der High-Flyer dieses Jahr bei US-Biotechs  werden.  

habe aber bisher noch kein stück bekommen;-((
warum weiß ich bisher auch noch nicht,die ganze story hört sich sehr gut an und sieht gut aus.  

...zischt ja seit Tagen ab wie eine Rakete !

heute, zumindest diese Woche dürfte die 5 Dollar-Marke geknackt werden was das Papier für Fonds interessant macht.  

habe ca.40% gewinn mitgenommen,dass ding steht auch immer noch auf meiner watchlist,aber aufregen tut es mich schon,dass ich zu früh raus bin.
über 100%wären hier drin gewesen oder wahrscheinlich noch mehr?
wo endet die reise?  

Press Release Source: CytRx Corporation

CytRx RNAi Subsidiary, RXi Pharmaceuticals, Announces Worldwide Research and Therapeutic RNAi Licensing Agreement with Cold Spring Harbor Laboratory
Monday March 19, 8:30 am ET


LOS ANGELES--(BUSINESS WIRE)--CytRx Corporation (NASDAQ:CYTR - News) today announced that its majority-owned subsidiary, RXi Pharmaceuticals Corporation (RXi), has secured a non-exclusive, worldwide research and therapeutic license from Cold Spring Harbor Laboratory to their short hairpin RNAi technology (shRNAi). The licensed technology potentially allows for the more efficient triggering of RNA interference (RNAi) and includes the use of short hairpin RNAis (shRNAis) either delivered as RNA compositions or encoded by DNA constructs. Patents covering this technology are currently pending. Financial terms were not disclosed for competitive reasons.
"With this license for all human therapeutic areas, we gain the well-validated advantage of shRNAi - which is reported to be up to 10- to 100-fold more potent compared with standard siRNA," said Tod Woolf, Ph.D., RXi's President and CEO. "This license supports our activities to accumulate a broad technology portfolio of RNA chemistry, and configuration and delivery technology, and marks another step in our construction of a world-class RNAi therapeutics company."

The technology licensed by RXi was developed in the laboratory of Gregory J. Hannon, Ph.D., a Howard Hughes Medical Institute Investigator at Cold Spring Harbor Laboratory. Dr. Hannon, who is a co-founder and member of RXi's scientific advisory board, is also a leading expert on oncogene pathways and was formerly an advisor to Alnylam Pharmaceuticals. Dr. Hannon's laboratory is credited with discovering the mechanism of RNAi in human cells (RISC/siRNA), as well as developing shRNAi technology.

REST WIE ÜBLICH.  

In USA wird bei CYTRX (CYTR) ein neuer Run erwartet. Wenn die 4 Dollar überwunden sind (heute 3,80 $)schätzt man, dass es sehr schnell auf die 5-Dollar-Marke und deutlich drüber geht. Bis Jahresende werden noch eine Reihe posiver News erwartet. Denke es lohnt sich dieses Papier wieder im Blick zu haben, könnte sich lohnen.  

Heute steigt CYTR weiter, um 5,5% auf 3,81 Dollar. Am Montag stehen zwei Präsentationen vor Investoren an. Zudem tanzen wir knapp unter der 200-Tage-Linie. Die Aktie hat einige Fantasie was diverse News in den nächsten Monaten angeht. Da sollte sich aber jede/r ein eigens Bild machen, könnte sehr interessant werden.

 

:-)))

Sobald der massive Wiederstand bei 0,83 € durchbrochen ist, wäre genug platz nach oben, bis 1,40 €   

Bin ja mal gespannt, ob wir heute die 0,83 € knacken !! Gestern waren wir jedenfalls kurz davor ! :-)

WKN: 922012

Dies soll keine Handelsaufforderung darstellen !!

 

So wie es aussieht werden wir die 0,83 € nicht so schnell knacken. Hhmmmm....  werd mich dann solange bei Novolos Therapeutics A0F6DX umsehen.