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YM BIOSCIENCES REPORTS FISCAL FIRST QUARTER 2010 OPERATIONAL AND FINANCIAL RESULTS
Date:11/11/2009

ic Investigation Plan (PIP) to the EMEA forthwith which, if approved by the Pediatric Committee (PDCO) would support a submission for marketing authorization. OSAG reports that it continues to recruit in a Phase III trial in adult glioma patients and a Phase IIb/III trial in pancreatic cancer patients. - Innogene Kalbiotech PTE Ltd. (IGK), CIMYM's licensee in South East Asia, has reportedly received marketing approval for nimotuzumab in the Philippines and Indonesia and in January 2009, the National Cancer Centre of Singapore announced that it was launching a worldwide Phase III, 710-patient trial of nimotuzumab in the post- operative or adjuvant setting in head and neck cancer. This trial is in addition to the on-going investigator-initiated Phase II trial in locally advanced head and neck cancer and the initiation of a Phase II trial in cervical cancer being conducted by IGK. - Nimotuzumab reportedly received approval for marketing in Mexico, bringing to 23 the number of countries that are now reported as having approved the drug for sale in specific indications.

For calendar 2010, YM BioSciences anticipates an extensive roll-out of important data concerning nimotuzumab's clinical utility and continued differentiation from the other marketed drugs in its class. Anticipated clinical data for calendar 2010 include:

    -   Final Phase III pediatric glioma data (Europe)
    -   Phase III adult glioma data (Europe)
    -   Phase II pediatric glioma data (North America)
    -   Phase II gastric cancer data (Japan)
    -   Phase II first-line non-small cell lung cancer data (Japan)
    -   Phase II esophageal data (Brazil)

AeroLEF(R)

YM continues to prepare its second late-stage product, AeroLEF(R), for further development internationally. After consulting with regulatory bodies in Euro
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SOURCE YM BioSciences Inc.
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