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BioWorld - Monday, December 29, 2025
Breaking News: BioWorld Science 2025 Year in ReviewBreaking News: BioWorld 2025 Year in ReviewBreaking News: BioWorld MedTech 2025 Year in ReviewBreaking News: Trump administration impacts continue to roil the life sciences sector
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BioWorld Science, Cancer
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European CHMP formally adopts positive opinion for IDM Pharma's Mepact in osteosarcoma

Dec. 30, 2008

FDA approves Novartis' Gleevec for recurrence following surgical removal of a GIST

Dec. 30, 2008

Drais and Diatos sign global license agreement for cancer drug DTS-108

Dec. 30, 2008

Preclinical profile of CAL-101 in hematological cancers disclosed

Dec. 30, 2008

FDA grants marketing authorization to Antisoma's oral fludarabine phosphate in CLL

Dec. 29, 2008

ArQule presents update on development of ARQ-621 and ARQ-761

Dec. 29, 2008

CHMP recommends orphan drug status for Immunomedics' radiolabeled hPAM4

Dec. 29, 2008

SuperGen reports preclinical data for its panel of novel drugs for cancer

Dec. 29, 2008

ArQule signs definitive license agreement with Daiichi Sankyo for selective c-Met inhibitor ARQ-197

Dec. 29, 2008

FDA grants orphan drug designation to TransMolecular's 131I-TM-601 for melanoma

Dec. 29, 2008
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