Research Update
April 27 2006 - 8:02AM
UK Regulatory
YM BioSciences' partner, Oncoscience AG, commences patient treatment in
phase III trial in Germany with nimotuzumab
MISSISSAUGA, ON, April 27 /CNW/ - YM BioSciences Inc. (AMEX:YMI, TSX:YM,
AIM:YMBA), the cancer product development company, today announced that its
partner, Oncoscience AG, has commenced patient treatment for its Phase III
trial of nimotuzumab in combination with radiation in children with diffuse,
intrinsic pontine (brain stem) glioma. The first three patients were recruited
within the last week.
The trial is a single arm study in which 40 children with inoperable
pontine glioma will be treated with radiation concomitant with nimotuzumab.
The primary clinical endpoints in the trial will be progression-free survival
with median survival as secondary endpoint. Clinical sites will be located in
Germany, Italy, Belarus and Russia and it is anticipated that recruitment
could be complete within approximately 12 months after the start of patient
enrolment. Based on historical data reporting progression-free survival and
median survival for this form of cancer of approximately 5.5 months and 8.5
months respectively, Oncoscience expects the trial should be completed in the
first half of 2007.
YM BioSciences has previously announced that it and its majority owned
subsidiary, CIMYM Inc., propose to file for authorization to conduct a trial
in a similar patient population in North America. In addition YM is
undertaking the clinical development of nimotuzumab in Non-Small Cell Lung
Cancer. YM's licensor, CIMAB SA and its parent, the Center for Molecular
Immunology, are conducting trials with nimotuzumab in glioma, breast,
esophageal, uterine cervix, prostate and head and neck cancer.
About Oncoscience AG
Oncoscience AG is a private biotech company based in Germany and is
focused in Oncology (nimotuzumab), Organ Transplantation (Lifor) and tumor
tissue banking including research in Genomics/Proteomics.
About YM BioSciences
YM BioSciences Inc. is a cancer product development company. Its lead
drug, tesmilifene, is a small molecule chemopotentiator currently undergoing a
700-patient pivotal Phase III trial in metastatic and recurrent breast cancer.
Published results from tesmilifene's first Phase III trial in the same
indication demonstrated a substantial increase in survival for women treated
with the combination of tesmilifene and chemotherapy compared to chemotherapy
alone, demonstrating that tesmilifene significantly enhanced the therapeutic
effect of chemotherapy.
In addition to tesmilifene and nimotuzumab, the Company is also
developing an anti-GnRH anti-cancer vaccine, Norelin(TM), for which Phase II
data have been released. YM's subsidiary DELEX Therapeutics Inc. is developing
AeroLEF(TM), a unique inhalation delivered formulation of the established
drug, fentanyl, to treat acute pain including cancer pain. This product has
completed a Phase IIa trial with positive results and a randomized Phase IIb
pain trial is ongoing. The Company also has a broad portfolio of preclinical
compounds shown to act as chemopotentiators while protecting normal cells.
Except for historical information, this press release may contain
forward-looking statements, which reflect the Company's current expectation
regarding future events. These forward-looking statements involve risk and
uncertainties, which may cause but are not limited to, changing market
conditions, the successful and timely completion of clinical studies, the
establishment of corporate alliances, the impact of competitive products and
pricing, new product development, uncertainties related to the regulatory
approval process and other risks detailed from time to time in the Company's
ongoing quarterly and annual reporting.
/For further information: Enquiries: Thomas Fechtner, The Trout Group
LLC, Tel. (212) 477-9007 x31, Fax (212) 460-9028, Email:
tfechtner(at)troutgroup.com; James Smith, The Equicom Group Inc., Tel.
(416) 815-0700 x 229, Fax (416) 815-0080, Email: jsmith(at)equicomgroup.com/
(YM. YMI)
END
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