Antisoma zu alten Höhen ?
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Eröffnet am: | 31.10.06 09:14 | von: DonCarlo | Anzahl Beiträge: | 994 |
Neuester Beitrag: | 25.04.21 01:33 | von: Tanjauqtwa | Leser gesamt: | 160.241 |
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Ah heheh okayyyy.... !!!!
Antisoma (LSE:ASM)
Last Price (USD) $7.00
Change 0.9 (14.75%)
Bid 6.95
Ask 7.00
Volume 2,542,365
Days Range 6.25 - 7.20
Last Trade 6/4/2010 4:47:23 AM
Rattert mal jemand die 7 weg dann fliegen wir weiter...danke !
Cash / Aktie müsste so ca. 8 pence sein..
Also wird knapp am Geld jetzt ?
Was fürn Witz..da ist kein bisschen Fantasie mit eingepreist..hehhee
Wieviele Aktien sind denn genau draussen ??
.............als Wiederstände werden sich jetzte wohl eher die Runden Marken erweisen wie die 0,1...0,15....usw
Im Bigchart intraday 1 minute war ein spike bis 7.40 !!!
http://bigcharts.marketwatch.com/charts/...mp;rand=851&mocktick=1
http://www.proactiveinvestors.com/companies/news/...by-fda--6296.html
Antisoma’s novel leukaemia treatment fast-tracked by FDA
Cancer focused biotechnology company, Antisoma (LON:ASM, OTC: ATSMY) told investors that its novel leukaemia treatment – the AS1413 DNA intercalator – has been granted a Fast Track designation by the US Food and Drug Administration (FDA).
The news has been welcomed by investors as the company’s shares advanced over 6.5% on the London Stock Exchange this morning.
FDA Fast Track designated drugs ordinarily qualify for Priority Review - an expedited review process available to drugs that offer major advances in treatment or provide a treatment where no adequate therapy exists. The novel DNA intercalator, AS1413 (amonafide L-malate), is being developed for the treatment of secondary acute myeloid leukaemia (secondary AML).
“This drug could represent a major advance in the options available to patients with secondary AML, and we look forward to completing the ongoing phase III trial and sharing the data with FDA and other regulators", Antisoma Chief Executive Glyn Edwards commented. "We're very pleased to have gained FDA Fast Track status for AS1413”.
The FDA's Fast Track programme is designed to facilitate the development of new drugs that have shown the potential to address an unmet medical need in a serious or life-threatening disease. The drug already has orphan drug status in both the US and the EU for the treatment of AML.