600% Kurspotential YM Biosciences 911799
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NEW YORK (AFX) - YM Biosciences Inc., (Nachrichten) which makes oncology and acute care drugs, said Friday its fourth-quarter loss widened missing analyst estimates due to a near twofold rise in the cost of licensing and product development.
For the quarter ended June 30, the Mississauga, Ontario-based company reported a loss of 8.6 million Canadian dollars ($7.7 million), or 16 Canadian cents (14 cents) per share, compared with 6.5 million Canadian dollars, or 18 Canadian cents per share, during the same period last year.
Revenue for the fourth quarter more than tripled to 1.1 million Canadian dollars ($980,000), from 300,000 Canadian dollars last year.
Licensing and product development expenses for the fourth quarter grew to 5.9 million Canadian dollars from 4.5 million Canadian dollars for the same quarter in 2005
Analysts polled by Thomson Financial forecast a loss of 12 cents per share and revenue of $420,000.
For the fiscal year, the company posted a net loss of 25.8 million Canadian dollars ($23 million), or 59 Canadian cents (52 cents) per share, compared with a net loss of 15.9 million Canadian dollars, or 47 Canadian cents per share, last year.
Licensing and product development costs nearly doubled to 20.2 million Canadian dollars from 11 million Canadian dollars last year.
Revenue for the year rose to 2.5 million Canadian dollars from 1.5 million Canadian dollars last year. YM BioSciences said the increases were primarily due to increased interest income resulting from larger short-term deposits compared with the previous year.
Quelle: http://www.finanznachrichten.de/...ichten-2006-09/artikel-7031524.asp
Aber alles in allem bin ich optimistisch....->Möglickeit nochmal ein Paar stücke einzusammeln
YM BioScience receives clearance to import nimotuzumab for clinical research in the US
MISSISSAUGA, ON, Sept. 25 /PRNewswire-FirstCall/ -- YM BioSciences Inc. (Nachrichten), a company engaged in the acquisition, development and commercialization of oncology and acute care products, today announced that the Office of Foreign Assets Control (OFAC) of the US Treasury Department has approved a license that allows YM BioSciences' wholly-owned U.S. subsidiary to import nimotuzumab into the United States for the purpose of clinical trials in pediatric patients with pontine glioma. Nimotuzumab is a monoclonal antibody that targets the Epidermal Growth Factor Receptor (known as EGFR) and was developed at the Center for Molecular Immunology affiliated with the University of Havana.
As a result of the OFAC license, YM BioSciences plans to submit an IND to the FDA to allow the investigation of nimotuzumab for the treatment of children with intrinsic diffuse pontine glioma. Upon FDA granting permission for the IND to proceed nimotuzumab, to the knowledge of the company, would be the first anti-cancer drug from Cuba to be used in clinical trials in the US.
"Diffuse pontine glioma is an inoperable malignant brain cancer that only affects children and, furthermore, it is a treatment resistant tumor so that children currently suffering from it have few treatment options," said David Allan, Chairman and CEO of YM BioSciences. "With this license from OFAC, we propose to submit an IND to the FDA to investigate nimotuzumab, thus potentially allowing US children access to the drug through a controlled clinical trial setting while collecting efficacy and safety data. Nimotuzumab has been available to children in other countries through their participation in clinical trials since 2004. At present median survival following diagnosis and treatment with radiation or chemoradiation is approximately 8.5 months, and median survival after recurrence following treatment is approximately three months."
Preliminary data from a Phase II nimotuzumab monotherapy study in Germany in pediatric high-grade glioma were presented at SIOP in 2005 and at ASCO in 2006. Data from this study formed the basis for a currently ongoing Phase III trial, combining nimotuzumab with radiation, in Europe through YM BioSciences' licensee OncoScience AG. Final results of that Phase II trial were presented at the 38th Congress of the International Society of Paediatric Oncology, Geneva, Switzerland, September 18, 2006.
The OFAC license permitting the import of nimotuzumab is an important first step towards preparing to initiate US clinical trials, and provided that the FDA concurs with the design a trial in diffuse intrinsic pontine glioma will be undertaken in numerous US and Canadian hospitals with the principal investigational site being the Hospital for Sick Children in Toronto, Canada. The current OFAC license allows the import of nimotuzumab for use in clinical trials only. The commercialization of the drug would require an additional license from OFAC.
Nimotuzumab, which is currently approved in India, China, Argentina, and Columbia as well as Cuba, was recently licensed by YM to Daiichi Pharmaceutical Co. for the Japanese market. In Europe and Canada, the drug is in numerous clinical trials including non-small cell lung cancer, pediatric glioma and refractory solid tumours (principally colorectal). That latter study evaluated nimotuzumab as monotherapy. The study was conducted at The Princess Margaret Hospital in Canada in 2006 and demonstrated significant clinical benefit in this highly refractory patient population. Data from this study will be submitted to upcoming medical meetings in 2007.
27.09.2006 13:10
YM BIOSCIENCES INC.: AeroLEF(TM) phase IIb interim review
YM BioSciences (Nachrichten) Announces AeroLEF(TM) Phase IIb Interim Review
- Benefit observed compared with placebo; Clinical trial to continue as
planned -
MISSISSAUGA, ON, Sept. 27 /CNW/ - YM BioSciences Inc. (AMEX:YMI, TSX:YM,
AIM:YMBA), a company engaged in the acquisition, development and
commercialization of oncology and acute care products, today announced that
its DELEX Therapeutics division has received the results of an interim
analysis on the first 67 patients from its randomized, placebo-controlled
Phase IIb trial (DLXLEF-AP4) of AeroLEF(TM) for the treatment of moderate to
severe acute pain in post-surgical patients. The data indicated that AeroLEF
provided benefit compared to placebo, however the difference between the
treatment arm and placebo arm had not yet achieved the significance level
predefined in the study protocol and therefore the study will continue as
planned to enroll the original target of 99 randomized patients.
"This preliminary review indicates that we should continue to advance the
AeroLEF phase IIb study to full enrollment," said David Allan, Chairman and
CEO of YM BioSciences. "We look forward to analyzing the full data set at the
completion of the study early next year."
AeroLEF(TM) is a unique, inhaled-delivery composition of free and
liposome encapsulated fentanyl, for the treatment of moderate to severe acute
pain, including cancer pain. The Phase IIb study consisted of two parts.
Part I was an open label trial of 21 patients to allow investigators to gain
familiarity with administration of the product. Part II is a randomized,
double-blinded, and placebo-controlled trial of 99 patients, and is designed
to evaluate the safety and efficacy of multiple doses of AeroLEF(TM) for
management of pain in post-surgical patients following elective orthopedic
surgeries. The primary endpoint for this study is the Summed Pain Relief plus
Pain Intensity Difference (SPRID) scores during the first four hours after the
start of the initial dose. Secondary endpoints include Time to Effective Pain
Relief, as well as six safety endpoints.
Preliminary results from the open label portion of the DLXLEF-AP4 trial
will be presented at the American Society of Anesthesiologists Annual Meeting,
McCormick Place, Chicago, IL, on October 17, 2006 at 9:00 a.m. Central.
END
Quelle: PR Newswire
Ich hab nur gelesen des da ein neuer Top-Ranked-Analyst(Katherine Kim) ist.
Gab es da ein negatives Statement?
Oder sind das noch die Nachwehen von der Fehlgeschlagenen AeroLEF(TM) Studie?
Kann ja nicht alzu positiv gewesen sein....
ich las heute auf http://www.boersenwelt.de/xist4c/web/...hillipps_id_279__dId_100_.htm dass hier sehr bald Ergebnisse erwartet werden.
könnte aktuell nen guter Einstiegszeitpunkt sein,Meinungen?
Aber die Umsätze sind in den letzten Tagen (Amex) deutlich gestiegen...Und dabei hat sich der Kurs nicht gerade positiv entwickelt!
Ist da was im Busch?
http://quicktake.morningstar.com/AlertNewsWire/...J0003&pgid=qtqnCom1
Weiß jemand, was da los ist?
Könnten das vielleicht Insider-Käufe sein vor anstehenden Nachrichten?
Aber warum macht der Kurs keine Sprünge bei solchen Umsätzen?