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BioWorld - Monday, August 3, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 18, 2007

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A DYRK3 inhibitor shows potential for anemia therapy

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New antidiabetic agents imparted in recent patents

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Signs of activity seen with CPX-351 in leukemia, myelodysplastic syndrome

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Phase II data on VNP-40101M in elderly AML patients reported

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New therapeutics for cancer covered in recent patent literature

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Recent Pharmacopeia patent reports novel antiparkinsonian agents

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Wyeth Pharmaceuticals reports positive results from two phase III clinical studies of Pristiq

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Oxford Biomedica initiates phase I/II trial of Prosavin for Parkinson's disease

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FDA Cardio-Renal Advisory Committee requests further study of Solvay's tedisamil

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FDA accepts ProEthic's NDA for PRO-513 for migraine headaches

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GENimmune's HCV monoclonal antibody receives orphan medicinal product designation

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FDA grants orphan drug status to Isis Pharmaceuticals' ISIS-333611 for ALS

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ImClone initiates phase II clinical trial of IMC-1121B for metastatic malignant melanoma

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Idera Pharmaceuticals initiates phase Ib trial of IMO-2055 for non-small cell lung cancer

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Recordati acquires Orphan Europe

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Novartis initiates phase II trial of QVA-149 for obstructive pulmonary disease

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FDA advisory votes against approving Merck & Co.'s NDA for nonprescription Mevacor

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Arena initiates BLOSSOM and BLOOM-DM phase III trials of lorcaserin for obesity

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Phase II trial of ofatumumab in diffuse large B-cell lymphoma begins

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MicroIslet holds pre-IND meeting with FDA regarding human clinical trial of MicroIslet-P

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FDA accepts for review MGI Pharma's NDA for Aquavan

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MediGene launches Veregen in the U.S. for genital and perianal warts

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Chugai's Xeloda obtains Japanese approval for new indication in colon cancer

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The CHMP of the EMEA recommends refusal of Neurochem's MAA for Kiacta

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GSK receives FDA complete response letter regarding cervical cancer vaccine Cervarix

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EMEA issues positive opinion recommending conditional approval of GSK's Tyverb

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