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BioWorld - Friday, December 5, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Sep. 2, 2009

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Letrozole monotherapy better than sequential treatment with tamoxifen in breast cancer patients

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Celladon and Momentum Research complete enrollment in phase II study of Mydicar

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Mitsubishi Tanabe Pharma reports results from second quarter 2009

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FDA grants orphan drug designation to Delcath Systems' doxorubicin in HCC

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Advanced Life Sciences reports results from nonhuman primate study of Restanza in anthrax

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TransPharma Medical completes phase II ViaDerm-hPTH(1-34) trial in osteoporosis

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Icagen reports topline results of phase IIa senicapoc study in allergic asthma

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Catalyst Pharmaceutical Partners licenses rights to new GABA aminotransferase inhibitors

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Cimzia approved for moderate to severe rheumatoid arthritis in Canada

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Amgen claims chemokine CXCR3 receptor antagonists for asthma and other disorders

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ACAT-2 inhibitors for the treatment of lipoprotein disorders disclosed by Kitasato Institute

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Medivir selects cathepsin K inhibitor MIV-711 for development in bone diseases

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Novavax reports results from phase II trial of trivalent VLP seasonal influenza vaccine

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Lilly describes kappa opioid receptor antagonists for the treatment of ethanol use disorders

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Adding colesevelam to a statin and ezetimibe lowers LDL-cholesterol in familial hypercholesterolemia

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Novel prodrugs of antifungal agents in early development at Eisai

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Vernalis presents Chk1 inhibitors for the treatment of cancer and other conditions

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Novel DNA-damaging platinum complexes designed by Universitat de Barcelona

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TRITON-TIMI 38 substudy suggests PPIs are safe with clopidogrel and prasugrel in ACS patients

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Bristol-Myers Squibb acquires Medarex

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First clinical results for BAY-60-4552 in biventricular heart failure reported

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FDA requests additional clinical data from SkyePharma for Flutiform NDA in asthma

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ON-TIME II analysis shows benefit of tirofiban in diabetic STEMI patients

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Initiation of phase II clinical trial of ALX-0081 in patients undergoing PCI

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Sinovac Biotech's H1N1 vaccine approved in SFDA expert meeting

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Geron presents data to FDA in relation to clinical hold on IND for GRNOPC-1

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