Antisoma zu alten Höhen ?

Na hier brauchst du auch ned Babysitten , selbstläufer imo ! :-)  

PPS ist am EOD amd HOD festgenagelt...sieht doch gut aus...  

der Nase draufstoßen  

Die Tiefstände nach dem Absturz sind hier vorbei.
Chart sieht Lecker aus und die News sind doch Superb..
Asco fängt morgen an und soweit ich weiss wird Antisoma 6 Präsentationen machen ?
Tick Tock closed @ HOD immer grosse grüne Kerzen bitte :-)  

 

sogar höher.
So einen Tiefstand haben wir letztes Jahr gehabt.

Behandlungsmethoden für Krebs, eine Fläche von akutem medizinischem Bedarf.

Antisoma hat ein vielfältiges Portfolio von Produkten in der Entwicklung


AS1413 (amonafide L-malate)


A DNA intercalator in phase III  in secondary AML



AS1411


A DNA aptamer in phase II in AML




ASA404 (DMXAA)

A Tumour-Vascular Disrupting Agent (Tumour-VDA) in phase III in second-line NSCLC


http://www.antisoma.com/asm/products/

http://investorshub.advfn.com/boards/board.aspx?board_id=17986

danke für das teamwork...ohne gross was zu sagen haben wir da  zeitgleich zusammengearbeitet..
Sozusagen seelische verwantschaft ???   ..lol :-)
Naja...man muss ja nicht immer alle geheimnisse preisgeben..
Das ding geht seinen Weg...da bin ich mir ziemlich sicher.. :-)  

Grünen dicken Kerzen sprechen für sich..wer jetzt nicht dabei ist dem kann man nicht helfen..45mill PFUND CASH !!!!
Okay das andere Medikament war flop aber dafür wird auch kein cash merh verbrannt..fokus auf die anderen !!
Un die sind "promising" !!  

heute weiter nach oben gehen, so ausgebombt wie die Aktie war.
Haben ja auch auf TH geschlossen

http://twitter.com/mikehavrilla/statuses/15324498118

...und der ist schon wer im Bio-Sektor!

http://seekingalpha.com/author/mike-havrilla
About Mike Havrilla

Mike Havrilla is a stock index developer, pharmacist, and writer with experience that includes online investing since August 1997 and writing for investors since April 2007 with a focus on the healthcare sector and medical innovation. Mike holds Doctor of Pharmacy (2003) and Bachelor of Science (Biology) (1998) degrees from the University of Pittsburgh and worked in the pharmaceutical industry for Wyeth prior to pharmacy school.

ich hab mit den twitterkram nix am hut und melde mich wegen des artikels sicher nicht an.

Cancer drug specialist Antisoma gained 20.8 per cent to 6p after the US Food and Drugs Administration gave its leukaemia treatment "fast track designation," allowing it to accelerate development. Dealers also noted that Antisoma was due to present to the oncology industry's annual conference this weekend.

www.ft.com/cms/s/0/e1003c70-6f71-11df-9f43-00144feabdc0.html

Das wird schon alleine wegen der ASCO sehr interessant !  :-)
Welche heute anfängt... :-)  

Mit den 45mill Pfund lässts sich ja ne weile weiterforschen und da Kosteneinsparungsprogramm ist auch durch soweit ich das ner PR vor zwei Monaten herauslesen kann.
Also das ganze siehr SEHR vielversprechend aus..sozusagen richtig "lala".   :-)  

 

http://www.londonstockexchange.com/exchange/...=GB0055696032GBGBXSSMM

 

Bid 6.60
Ask 6.80
Volume 217,706  

wo seht ihr das mögliche KZ im Moment
 

12 cent  

 

 

http://www.antisoma.com/asm/media/press/pr2010/2010-05-17/

London, UK, and Cambridge, MA: 17 May 2010 – Cancer drug developer Antisoma plc (LSE: ASM; USOTC: ATSMY) today publishes its Interim Management Statement for the period from 1 January to 16 May 2010.

Antisoma’s CEO, Glyn Edwards, said: “We have two promising cancer drugs, AS1413 and AS1411, both of which we expect to report key trial data during the next year. Having taken measures to reduce our costs, we expect our cash resources to take us well past these trial results.”

Joint Chairman and CEO’s statement
We are determined to bounce back strongly from the recent disappointment over ASA404, centred on the termination in March of a phase III trial evaluating the drug as a first-line treatment for lung cancer. We recognise that ASA404 was considered the Company’s most significant asset, but we are confident that Antisoma’s strategy of investment in a diversified portfolio of products remains sound. We have had to make tough decisions in light of the ASA404 result, but believe that we have the product assets, people and financial resources to build value for the future.

AS1413 – rapid recruitment continues in phase III trial
AS1413 is a novel chemotherapy treatment that we are testing in a large, multi-country, randomised phase III trial in patients with secondary acute myeloid leukaemia (secondary AML). The trial, known as ACCEDE, has now recruited over 75% of its target of 450 patients, putting us on course to complete enrolment this calendar year. Following collection and processing of data, we expect to announce results of the study during the first half of 2011.

There is interest from potential licensing partners for AS1413. We have decided to take a pragmatic stance to realising the value of this drug, and have therefore widened our partnering discussions to include US rights, which we had previously planned to retain. However, we will only strike a deal ahead of the phase III data if the terms are sufficiently favourable.

We believe that AS1413 could ultimately find application in a number of blood cancer settings, with potential sales running to hundreds of millions of dollars annually. A presentation at the American Association of Cancer Research (AACR) Annual Meeting during April reinforced the differentiation of AS1413 from currently available leukaemia treatments and its potential to provide unique benefits for patients. Three presentations with relevance to AS1413 will be made at the American Society of Clinical Oncology (ASCO) Annual Meeting in June; abstracts will be available on the ASCO website (www.asco.org) from 20 May.

AS1411 – phase IIb trial now underway
AS1411 is the most advanced aptamer in trials for cancer. It is now in a 90-patient phase IIb study in patients with AML. This trial follows an earlier randomised phase II trial in AML, which reported positive results at the 2009 ASCO meeting: in that study, two different doses of AS1411 in combination with cytarabine chemotherapy produced response rates of around 20%, whereas the response rate in patients receiving chemotherapy alone was 5%. Addition of AS1411 to chemotherapy was not associated with any significant additional side-effects. Headline data from the phase IIb study are expected in the first half of next year.

Recent and forthcoming conference presentations highlight the broad potential of AS1411. Non-clinical data presented at AACR in April showed activity in a model of colorectal cancer and positive findings when AS1411 was combined with a number of approved treatments for blood cancers. At the ASCO meeting we will have three presentations on AS1411, including updated findings from the first phase II clinical trial in AML and data from a phase II clinical trial in renal cancer.

DCAM auto-immune programme progressing towards partnering
We have an important pre-clinical programme in auto-immune diseases. This comprises a series of molecules collectively known as DCAMs (dendritic cell auto-immune modulators). They are highly specific, small-molecule inhibitors of wild-type Flt3, and are designed for oral treatment of various auto-immune conditions. Positive results have already been achieved in animal models of inflammatory bowel disease and rheumatoid arthritis, and we are now working towards establishing a licensing partnership for further development of the programme.

Cash conservation measures enacted
We are no longer anticipating further revenues from the ASA404 programme, and have therefore taken steps to reduce our cash utilisation and ensure that our funds take us comfortably through key clinical data on AS1413 and AS1411. We announced on 29 March that our unaudited cash position as of the end of February 2010 was GBP 45.1 million.

Board and management changes
Regrettably, we have had to restructure the business and make headcount reductions as part of our effort to conserve cash resources. As part of the restructuring, our former Chief Operating Officer, Dr Ursula Ney, has left the Company and the Antisoma Board. Ursula made a very significant contribution to the development of Antisoma, and we wish her well with future ventures. Two other members of the Senior Management Team, Julio Gagne and Kevin Kissane, have also left the Company, and our total headcount has now been reduced to around seventy-five.

Outlook
We look forward to a number of important clinical milestones in the near term, notably phase III data on AS1413 and phase IIb data on AS1411, both of which we expect during the next year.