Cell Therapeutics (CTIC) Il mio nome è Therapeutic! ...Cell therapeutic !.....2° atto (7 lettori)

patt

Forumer storico
Cell Therapeutics, Inc. (CTI) Granted U.S. Patent for New Potent Antitubulin Agents With Anti-Cancer Activity
Monday April 10, 7:00 am ET
Preclinical Studies Demonstrate Antiproliferative Activity in Tumor Cell Lines Resistant to Standard Chemotherapy



SEATTLE, April 10 /PRNewswire-FirstCall/ -- Cell Therapeutics, Inc. (CTI) (Nasdaq: CTIC; MTAX) announced today that the United States Patent and Trademark Office granted a patent for a new class of small molecule antitubulin agents with potent antiproliferative and tumor killing activity. CT-45099 is the first lead optimized agent from this class of compounds to advance into preclinical testing. The patent, owned by CTI's European subsidiary, Cell Therapeutics Europe S.r.l. (CTI-Europe), covers analogs of CT-45099 and will expire in April 2022. CT-45099 is protected by a U.S. and European patent already granted to CTI-Europe.
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Unlike the marketed taxane-based cancer drugs, Taxol® (paclitaxel) and Taxotere® (docetaxel), or even investigational new drugs like epothilones, which kill cells by stabilizing microtubules and preventing their disassembly, this class of agents blocks tubulin assembly and destabilizes microtubules during cell mitosis. Therefore, this class of agents has anti-tumor activity distinct from these other drugs. In addition, this new class of antitubulin agents is not susceptible to multi-drug resistance, one of the most common mechanisms by which cancer cells develop resistance to standard chemotherapies. CT-45099 and its analogs inhibit in vitro the growth of colon, lung, gastric, and prostate cancer cell lines, including cancer cells resistant to paclitaxel or doxorubicin treatment.

"This patent, and the new class of agents covered within, highlights our ability to take a well known target in cancer drug development, like tubulin, and apply our medicinal chemistry expertise to develop a novel class of anti-cancer agents that may possess superior anti-tumor activity over commonly used tubulin-stabilizing chemotherapy drugs," noted Alberto Bernareggi, Ph.D., Managing Director of CTI-Europe.

About Cell Therapeutics, Inc.

Headquartered in Seattle, CTI is a biopharmaceutical company committed to developing an integrated portfolio of oncology products aimed at making cancer more treatable. For additional information, please visit www.cticseattle.com.

This press release includes forward-looking statements that involve a number of risks and uncertainties, the outcome of which could materially and/or adversely affect actual future results. Specifically, the forward-looking statements contained in this press release include statements about future risks and uncertainties that could affect the development of CTI's tubulin binding compounds. These risks include, but are not limited to, preclinical, clinical, and sales and marketing developments in the biopharmaceutical industry in general, and in particular including, without limitation, the determinations by regulatory, patent and administrative governmental authorities, competitive factors, technological developments, costs of developing, producing and selling CTI's tubulin binding compounds, and the risk factors listed or described from time to time in the Company's filings with the Securities and Exchange Commission including, without limitation, the Company's most recent filings on Forms 10-K, 8-K, and 10-Q. CTI is under no obligation to (and expressly disclaims any such obligation to) update or alter its forward-looking statements whether as a result of new information, future events, or otherwise.




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Source: Cell Therapeutics, Inc.
 

carrodano

Forumer storico
Hanno toccato il fondo ?

Avevo preso 2000 CTIC venerdi' a 1.5

vendute oggi a 1.55, poi le ho viste salire salire........................

domani le riprendo
 

carrodano

Forumer storico
oggi in america è partita a 1.86, adesso è 1.81

anche ieri partita alta e poi fermata a 1.78

il minimo l'altro ieri a 1.69.
:-?
oggi da noi apertura e chiusura a 1.53

punta minima toccata in settimana 1.43
:-?
Oggi vendute mille sul saltino.

Altre mille in PTF, in questo caso sugli spalti.

Avete presente il DESERTO DEI TARTARI di BUZZATI
 

patt

Forumer storico
26 Aprile 2006


CELL THERAPEUTIC rende nota la prossima emissione di obbligazioni senior convertibili al 7,5% per un importo nominale complessivo di circa 33,2 milioni di dollari con scadenza 2011in cambio di obbligazioni senior convertibili subordinate per circa 39,5 milioni di dollari al 5,75% in circolazione con scadenza 2008 e di obbligazioni convertibili subordinate per circa 1,2 milioni di dollari al 5,75% in circolazione con scadenza 2008. Le Obbligazioni, si legge nella nota, oltre ad avere un interesse annuo del 7,5% e saranno convertibili in azioni ordinarie CTI nel rapporto di 478,519 azioni per 1000 dollari di valore nominale delle obbligazioni, pari a un prezzo iniziale di conversione di circa 2,09 dollari per azione, o 115% del prezzo di scambio medio ponderato delle azioni ordinarie di CTI in base al volume trattato nei cinque giorni precedenti il 20 Aprile 2006.
 

patt

Forumer storico
Cell Therapeutics, perdite nette a quota 53,2 mln nel I trim.2006

Cell Therapeutics (NASDAQ: CTIC - notizie) ha chiuso il primo trimestre 2006 con una perdita netta pari a 53,2 milioni di dollari. Nello stesso periodo dello scorso anno la società farmaceutica aveva rilevato un passivo di 39,132 milioni di dollari, inferiore dunque a quello attuale. La responsabilità dell'aumento delle perdite è da imputare principalmente alla gestione finanziaria, poiché la società ha dovuto affrontare una delicata operazione di ristrutturazione del debito, conclusasi lo scorso 28 aprile. La sola gestione operativa, sebbene non abbia praticamente generato ricavi in seguito alla vendita del prodotto Trisenox nello scorso luglio, ha fatto comunque un balzo in avanti rispetto al primo trimestre 2005, passando da -35,748 milioni a 26,747 milioni di dollari. Dal punto di vista patrimoniale, attività liquide per un valore pari a 50,3 milioni di dollari e un debito riorganizzato rendono l'amministratore delegato James Bianco ottimista sulla buona riuscita degli investimenti in corso.
Per ulteriori informazioni visita il sito di Finanza.com
 

patt

Forumer storico
dando un okkio al grafo di CTIC$ le quotazioni sono piuttosto compresse.....

il pennant (triangolo) sta diventando piuttosto strettino...a questo punto qualcosa deve accadere.....un break nella parte bassa..è inutile dirlo darebbe spazio a ulteriori decisi ribassi...e se il close di domani fosse anche appena piu' basso di quello di oggi ci dovremmo essere..quindi come stop ho messo gl'1,75$......mmentre il break degl'1,85(nn a caso corrisponde a diverse chiusure e massimi dell'ultima settimana ) lo vedrei come un segnale positivo ...




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patt

Forumer storico
Pixantrone Produces High Rate (77 percent) of Complete Tumor Disappearance in Patients with Relapsed Indolent Non-Hodgkin's Lymphoma
Tuesday May 16, 3:30 am ET
Substituting for Standard Anthracycline Chemotherapy May Offer Better Chance for Complete Remission


SEATTLE, May 16 /PRNewswire-FirstCall/ -- Preliminary results of a phase I/II study of pixantrone combined with fludarabine, dexamethasone, and rituximab for treatment of patients with relapsed indolent non-Hodgkin's lymphoma (NHL) will be presented today at the Rodman & Renshaw 3rd Annual Global Healthcare Conference in Monte Carlo, Monaco. The phase I/II study of the pixantrone combination regimen, known as FPD-R, produced a 95 percent overall response rate (ORR) with 77 percent of patients experiencing complete disappearance of their tumors (complete remission). Cell Therapeutics, Inc. (CTI) (Nasdaq and MTAX: CTIC) is also studying pixantrone in an ongoing phase III study in aggressive NHL, known as the EXTEND trial.
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In the phase I/II study, of the 22 patients evaluable for response, 95 percent achieved an objective response, including 77 percent who achieved complete response/unconfirmed complete response (CR/CRu) with 18 percent achieving a partial response (PR). At two years, overall survival is 85 percent, with a median failure-free survival of 25 months (range, three to 29 months). Predominant side effects (grade 3/4) were primarily hematological including neutropenia (76 percent), febrile neutropenia (8 percent), lymphopenia (76 percent), thrombocytopenia (20 percent) and anemia (4 percent).

"Although many regimens induce responses in patients with relapsed indolent NHL, many of the remissions are of relatively short duration," noted Jack W. Singer, M.D. Chief Medical Officer at CTI. "These data suggest that use of pixantrone with fludarabine, dexamethasone and rituximab not only offers a very high response rate, but impressive durability."

The webcast with slides will be available at www.cticseattle.com.

About Pixantrone and the FPD-R Regimen

This trial examines the safety and potential efficacy for pixantrone when substituted for mitoxantrone in the FND-R regimen (fludarabine, mitoxantrone, dexamethasone, rituximab) for patients who had failed prior treatment.

Patients received a median of 5.5 cycles of therapy. Cycles were every 28 days. Dosing was rituximab at 375 mg/m2 dl, fludarabine at 25 mg/m2/d d1-3, dexamethasone at 20 mg/d PO, d1-5 and pixantrone starting at 80 mg/m2 to 120 mg/m2.

About Pixantrone

Pixantrone is an investigational agent under development for the potential treatment of various hematological malignancies, solid tumors and immunological disorders. It was developed to improve the activity and safety of the anthracycline family of anti-cancer agents. Anthracyclines have been shown to be very active clinically in a number of tumor types. However, they are usually associated with cumulative heart damage that prevents them from being used in a large proportion of patients. Pixantrone has been designed to reduce the potential for these severe cardiotoxicities, as well as to potentially increase activity and simplified administration compared to the currently marketed anthracyclines.

About Cell Therapeutics, Inc.

Headquartered in Seattle, CTI is a biopharmaceutical company committed to developing an integrated portfolio of oncology products aimed at making cancer more treatable. For additional information, please visit www.cticseattle.com.

This press release includes forward-looking statements that involve a number of risks and uncertainties, the outcome of which could materially and/or adversely affect actual future results. Specifically, the risks and uncertainties that could affect the development of pixantrone include risks associated with preclinical and clinical developments in the biopharmaceutical industry in general and with pixantrone in particular including, without limitation, the potential failure of pixantrone to prove safe and effective for treatment of non-Hodgkin's lymphoma, determinations by regulatory, patent and administrative governmental authorities, competitive factors, technological developments, costs of developing, producing and selling pixantrone, and the risk factors listed or described from time to time in the Company's filings with the Securities and Exchange Commission including, without limitation, the Company's most recent filings on Forms 10-K, 8-K, and 10-Q. CTI is under no obligation to (and expressly disclaims any such obligation to) update or alter its forward-looking statements whether as a result of new information, future events, or otherwise.




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Source: Cell Therapeutics, Inc.
 

woolloomooloo

Forumer storico
patatino ha scritto:
At two years, overall survival is 85 percent, with a median failure-free survival of 25 months (range, three to 29 months).
Non capisco perchè nella loro nota non hanno aggiunto un 'compared to'
" Standard Anthracycline Chemotherapy ", visto che l'obiettivo della 'nota' è di far 'supporre' che sia migliore.
Infatti l' overall survival è il dato principale di comparazione dei farmaci sul cancro.

Se l'overall è uguale o peggiore, allora si guardano i 'side effects'
patatino ha scritto:
Predominant side effects (grade 3/4) were primarily hematological including neutropenia (76 percent), febrile neutropenia (8 percent), lymphopenia (76 percent), thrombocytopenia (20 percent) and anemia (4 percent).

e, in questo caso, sono quelli soliti per uno studio di fase I/II di questo tipo. Anche qui però i dati da soli dicono poco, bisogna andare a comparare la percentuale con il 'trattamento standard'.
 

patt

Forumer storico
ecco la notizia in italiano...



MARKET TALK: Cell T., volumi elevati con nuovi sbocchi per Pixantrone
MILANO (MF-DJ)--Scambi elevati, e pari a circa il 3,8% del capitale sociale, per Cell T.. Il titolo beneficia della possibile sostituzione, oggetto al momento di valutazione, della chemioterapia con il Pixantrone in regime di combinazione (FPD-R) nella fase III del trattamento dei pazienti con linfoma non-Hodgkin. Cell T. +4,49% a 1,35 euro. frc (END) Dow Jones Newswires May 16, 2006 08:31 ET (12:31 GMT) Copyright (c) 2006 MF-Dow Jones News Srl.
 

patt

Forumer storico
woolloomooloo ha scritto:
e, in questo caso, sono quelli soliti per uno studio di fase I/II di questo tipo. Anche qui però i dati da soli dicono poco, bisogna andare a comparare la percentuale con il 'trattamento standard'.



forte ritracciamento dai massimi....ora vediamo che diranno a wally....il preopen è "freddino"
 

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