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BioWorld - Thursday, April 18, 2024
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BioWorld Science
Sep. 21, 2007
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BIBW-2992 active in preclinical models and patients with non-small cell lung cancer
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Natural products for the treatment of sleep disorders
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Motexafin gadolinium studied in refractory lung cancer, patients with brain metastases
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Intra-Cellular Therapies outlines portfolio of proprietary compounds for FSD
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LigoCyte to develop anti-CD103 therapies with Biogen Idec
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Positive results for sanofi pasteur's low-dose H5N1 influenza vaccine
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Recent patents disclose novel therapeutic agents for cardiovascular disorders
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Discovery of agents for neurological disorders reported in recent patent literature
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MKC-1 well tolerated in phase II metastatic breast cancer trial
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Knee osteoarthritis pain relief observed with IDEA-033
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Preclinical antianginal activity of the sodium channel blocker F-15845
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Preclinical characterization of DX-2400, a novel fully human antibody against MMP-14
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Preclinical activity and pharmacokinetics of the novel PDE5 inhibitor lodenafil carbonate
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Astellas Pharma U.S. submits response to FDA action letter for once-daily FK-506
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Alexza to begin first of two phase III trials of AZ-004
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FDA recommends LipoNova continue autologous RCC vaccine development program
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Allergan to acquire Esprit Pharma and partner with Indevus on Sanctura brand
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GlaxoSmithKline submits application for SAD indication for Paxil tablet in Japan
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PEGylation and Pulmonary research units created by Nektar
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Evotec to acquire Renovis
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Patient enrollment completed in phase II trial of Gabapentin GR for menopausal hot flashes
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AVI BioPharma receives DoD contract for development of NeuGene antisense drug
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DelSite Biotechnologies enters technology evaluation agreement for GelSite polymer
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RDEA-806: a novel anti-HIV NNRTI safe and well tolerated in human studies
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TMC-125 NDA accepted for priority review in U.S.
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Campath approved in U.S. for first-line treatment for B-CLL
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Novel antifolates with improved activity against staphylococcal and enterococcal infections
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Lilly files for European approval of Alimta as first-line treatment of NSCLC
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Wyeth receives EMEA opinions on Torisel and Mylotarg
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The EC to authorize Yondelis commercialization for soft tissue carcinoma
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