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2004 MAY 6 - (NewsRx.com & NewsRx.net) -- YM BioSciences Inc. (YM) announced that the first patient has been dosed in its 700-patient phase III registration trial for metastatic breast cancer.
The international pivotal trial is designed to compare the overall survival differential resulting from the combination of YM's drug, tesmilifene, with the anthracycline, epirubicin, and cyclophosphamide against the use of epirubicin/cyclophosphamide alone in women with metastatic breast cancer.
"We are very pleased to have commenced this important trial on time, and anticipate to have completed enrolment in approximately 18 months," said Mr. David Allan, chairman and chief executive officer of YM BioSciences.
Tesmilifene is a small molecule chemopotentiator. In the first phase III trial, which enrolled 305 women, overall survival in women on the combination of tesmilifene with anthracycline (the standard of care in metastatic breast cancer) was greater than 50% longer than for women treated with the standard of care alone.
The drug has been clinically demonstrated to increase the effectiveness of the current principal chemotherapeutic drugs, anthracyclines and taxanes, ...
Source: HighBeam Research, Drug development company doses first patient in breast cancer study.