SIGA 3.10$
SIGA on bounce watch mit Ziel 3.50$
Quote:
QuoteWedbush lowers PT on $SIGA from 23$ to $11, maintains its outperform rating
SIGA on bounce watch mit Ziel 3.50$
Quote:
QuoteWedbush lowers PT on $SIGA from 23$ to $11, maintains its outperform rating
vagnum wrote:
QuoteMELA Sciences, Inc. Receives European Union Approval for MelaFind
Quote:
Pre-market: 6.70 +3.52 (110.69%)
vagnum wrote:
QuoteSIGA on bounce watch mit Ziel 3.50$Quote:
SIGA 3.30$ meine 3.50$ sind endlich in play.
CXM hat fda zulassung erhalten
b00n wrote:
QuoteCXM hat fda zulassung erhalten
war leider nicht dabei... du?
offenes gap bei 44.00$ läuft wenn der Markt läuft mmn.
call 50.00$?
ne cxm nicht dabei gewesen.
---
CYCC
PRESS RELEASE
Oct. 13, 2011, 7:00 a.m. EDT
Cyclacel Announces Data Safety Monitoring Board Recommendation to Continue the SEAMLESS Phase 3 Trial of Sapacitabine
Lead-in Portion of the Phase 3 Study Meets Prespecified Criteria Agreed in a SPA With FDA
Zürich (awp) - Der Pharmagigant Roche wird die amerikanische Anadys Pharmaceuticals für rund 230 Mio USD übernehmen. Die beiden Unternehmen hätten eine Vereinbarung über den Zusammenschluss getroffen, wonach Roche Anadys im Rahmen einer Bartransaktion für 3,70 USD je Aktien vollständig übernehme, heisst es in einer Mitteilung am Montag
http://www.google.com/finance?q=NASDAQ:ANDS#
Pre-market: 3.58 +2.54 (244.23%)
Leonator wrote:
QuoteZürich (awp) - Der Pharmagigant Roche wird die amerikanische Anadys Pharmaceuticals für rund 230 Mio USD übernehmen. Die beiden Unternehmen hätten eine Vereinbarung über den Zusammenschluss getroffen, wonach Roche Anadys im Rahmen einer Bartransaktion für 3,70 USD je Aktien vollständig übernehme, heisst es in einer Mitteilung am Montag
http://www.google.com/finance?q=NASDAQ:ANDS#
Pre-market: 3.58 +2.54 (244.23%)
nice, haste abgeräumt?
b00n wrote:
QuoteCXM hat fda zulassung erhalten
läuft weiter
Halozyme Announces Positive Results from Roche's Subcutaneous Herceptin Phase 3 Trial
Quote:
QuoteSAN DIEGO, Oct. 18, 2011 /PRNewswire/ -- Halozyme Therapeutics, Inc. (NASDAQ: HALO), a biopharmaceutical company developing and commercializing products targeting the extracellular matrix for the diabetes, cancer, dermatology and drug delivery markets, today announced that the Phase 3 HannaH trial, conducted by Roche, showed that women with HER2-positive early breast cancer who received a new, investigational subcutaneous (SC) injection of Herceptin® (trastuzumab), experienced comparable results to Herceptin given as an intravenous (IV) infusion. The SC administration takes around 5 minutes to administer whereas the IV formulation (the current standard) takes around 30 minutes to infuse. Since the subcutaneous administration is an injection under the skin it may allow patients to spend less time in hospital receiving their treatment versus the intravenous method. The ready to use formulation may also significantly reduce pharmacy time as no medicine preparation time is required.Display More(Logo: http://photos.prnewswire.com/prnh/20100302/LA63139LOGO)
"We are very pleased to see this important program achieve success in a Phase 3 pivotal clinical trial," said Gregory Frost, Ph.D., Halozyme's president and CEO. "The convenience of subcutaneous administration may provide another option for women living with early breast cancer."
No new safety signals were observed and adverse events were overall consistent with Herceptin IV. Data from the trial will be submitted for presentation at an upcoming medical meeting and will support a marketing application to regulatory authorities in the European Union in 2012.
Roche has additional ongoing trials of a subcutaneous formulation of MabThera® (rituximab), using Enhanze™ Technology in patients with CD20+ non-Hodgkin's lymphoma (NHL) and Chronic Lymphocytic Leukaemia (CLL).
Halozyme Therapeutics (NASDAQ:HALO): JMP Securities upgraded its rating on this company from Mkt Perform to Mkt Outperform and changed its price target to $9.
Radient Pharmaceuticals Corporation (Public, PINK:RXPC)
HOTZENPLOTZ wrote:
QuoteRadient Pharmaceuticals Corporation (Public, PINK:RXPC)![]()
Siehe Trade bei den Pennystocks.
Gruss
MMoser
HOTZENPLOTZ wrote:
QuoteRadient Pharmaceuticals Corporation (Public, PINK:RXPC)![]()
Hotzi ist wieder daaaaaaaa! Lange Zeit nix mehr von dir gehört, warst wohl wieder auf der Flucht vorm Kasperl und Seppel, häh??!!
____________________________________________
HALO 7.55$, hab vermutet, dass da noch was geht.
gruuuueeeess
vagnum wrote:
QuoteDisplay MoreHOTZENPLOTZ wrote:
Hotzi ist wieder daaaaaaaa! Lange Zeit nix mehr von dir gehört, warst wohl wieder auf der Flucht vorm Kasperl und Seppel, häh??!!
![]()
____________________________________________
HALO 7.55$, hab vermutet, dass da noch was geht.
gruuuueeeess
Hey Hallo! Freut mich! Hatte es mal mit Arbeit probiert... haha! Wenn ich jetzt nicht gleich alles verzock, werd ich die kalten Winterabende über wieder hier sein und mit meinen drei Lieblingen spielen, die ich das ganze Jahr über im Auge behielt (KERX, CLDX und das nun zu den Pennystocks verdammte RXPC). Wie läufts mit den Ziggis? Liebe Grüsse. Hotzi
PS. Sorry für OT
Halozyme Announces Positive Results From Phase 2 Ultrafast Insulin Trials in Patients with Type 1 and Type 2 Diabetes
Quote:
QuoteAN DIEGO, Oct. 21, 2011 /PRNewswire via COMTEX/ -- Halozyme Therapeutics, Inc. HALO +5.44% , a biopharmaceutical company developing and commercializing products targeting the extracellular matrix for the diabetes, cancer, dermatology and drug delivery markets, today announced positive results from two Phase 2 clinical trials of its ultrafast PH20 insulin analog formulations in patients with Type 1 and Type 2 diabetes. Both trials met the primary endpoint of non-inferiority of HbA1C compared to the insulin analog comparator, with superior reductions in post-prandial glucose excursions in the PH20 insulin analog arms. Compared to insulin analog alone, PH20 insulin analog use resulted in a greater than 50% increase in the proportion of patients able to consistently achieve AACE (American Association of Clinical Endocrinologists) guidelines for post-prandial glucose targets in both Type 1 and Type 2 patients. Across all of the treatment groups, there was no meaningful difference in hypoglycemia incidence or event rates. Hypoglycemia events were generally mild, and adverse events with PH20 insulin analog formulations were similar to those observed during the insulin analog comparator phase.
@ Hotzi, Hab dir ne PM geschickt! Die e-cigs, haha. Jetzt kann man die Dinger auch am Kiosk kaufen.
lg und good trading
PRESS RELEASE
Oct. 24, 2011, 6:00 a.m. EDT
Arrowhead Research Corporation Acquires Roche RNA Assets and Site
Three New Delivery Technologies, Broad RNAi IP, and Advanced Operations to Drive Clinical Development, Partnerships, and RevenueRoche Takes Equity Stake in Arrowhead and Rights to Negotiate Future RNAi Candidates
We are offering 1,000,000 shares of our Common Stock in this offering at a public offering price of $0.40 per share. This is a best efforts offering being made directly by Arrowhead, without an underwriter or placement agent. We are not required to sell any specific number or dollar amount of securities in this offering, but will use our best efforts to sell the securities offered. We will receive all of the proceeds from any securities sold in this offering. If we sell the maximum number of shares offered by this prospectus supplement, the total gross offering proceeds to us, before offering expenses, will be approximately $400,000. This offering will continue until the earlier of the sale of all shares offered by this prospectus supplement or October 31, 2011.
Our Common Stock is quoted on The NASDAQ Capital Market under the symbol “ARWR.” On October 21, 2011, the last reported sales price of our Common Stock on The NASDAQ Capital Market was $0.46 per share.
Alexza Pharmaceuticals Announces Submission of European Marketing Authorization Application for Adas
Quote:
QuoteAlexza Pharmaceuticals, Inc. (Nasdaq: ALXA) announced today that it has submitted its ADASUVE Marketing Authorization Application (MAA) to the European Medicines Agency (EMA). ADASUVE uses Alexza's proprietary Staccato system, an oral inhalation technology that provides rapid systemic delivery of a thermally-generated aerosol of loxapine. The ADASUVE MAA seeks approval for the rapid control of agitation in adult patients with schizophrenia or with bipolar disorder. The Staccato system offers patients a rapid onset of therapeutic effect in a non-invasive, reliable and patient-friendly manner.Display More"During the last six months, we have conducted pre-submission meetings with both our Rapporteur and Co-Rapporteur, and we believe we have a good understanding of their expectations for our ADASUVE MAA submission," said James V. Cassella, PhD, Senior Vice President, Research and Development at Alexza. "Our submission has been developed to address their inputs and feedback, and we are very excited to have the European review process initiated."
Dr. Cassella continued, "In addition to information from the US NDA, our ADASUVE MAA submission contains additional analysis of the primary efficacy data, and a comprehensive comparison of Staccato loxapine and other injectable drugs used to treat agitation."
Alexza projects that there may be up to eight million adults in Europe who will develop schizophrenia or bipolar disorder in their lifetimes. Agitation is a common symptom among patients suffering from schizophrenia and bipolar disorder. Alexza's market research studies with schizophrenia patient caregivers and bipolar disorder patients indicates these patients currently experience an average of 11 to 12 episodes of agitation each year.
"Our MAA submission is another important step in the development of ADASUVE," stated Thomas B. King, President and CEO of Alexza. "We are optimistic that we will receive timely European review, as we begin to work with our partner Grupo Ferrer, in executing our European commercialization strategy. We believe ADASUVE offers an innovative therapeutic option for the treatment of agitation associated with schizophrenia or bipolar disorder."