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BioWorld - Wednesday, March 11, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Nov. 24, 2015

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ProMetic partners with ProThera to develop plasma-derived IAIP

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Spring Bank plans phase II trial of SB-9200 and Viread in HBV infection

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University of Adelaide to conduct phase I study of AmpliPhi's AB-SA01

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Galapagos begins phase I study of GLPG-1972

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Daiichi Sankyo doses first subject in phase I study using Anticalin technology

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Boston Pharmaceuticals launched to develop drugs for complex diseases

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Autologous CBL-B-silenced cell therapy is feasible in patients with solid tumors

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MediciNova to begin phase IIa study of MN-001 for hypertriglyceridemia in patients with NASH

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Phase Ib trial of Aptose's APTO-253 placed on hold

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Immune responses, survival improvements seen with uveal melanoma DC vaccine

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Benepali is first biosimilar etanercept recommended for approval in E.U.

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Vitamin D analogue DP-001 may be superior for treating secondary hyperparathyroidism

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First preclinical results presented for a novel, noncovalent BTK inhibitor

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CHMP recommends approval of Briviact

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AstraZeneca patents ATM kinase inhibitors

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Kineta discloses antiviral RIG-I pathway modulators

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Bristol-Myers Squibb reports GPR40 modulators

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U.S. Department of Health & Human Services introduces CB1 receptor ligands

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Merck KGaA patents PARP-1/TNKS inhibitors

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NEO-214 shows efficacy against gliomas

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AstraZeneca sells U.S. rights to Entocort to Perrigo

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Pharmacological chaperone shows promise for GM1 and Morquio B lysosomal diseases

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CHMP recommends approval of Episalvan to treat partial thickness wounds in adults

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Metastatic colorectal cancer study shows administration of neratinib with cetuximab is feasible

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FDA clears IND for phase IIa trial of Generon's F-652 for alcoholic hepatitis

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FDA approves Opdivo for renal cell carcinoma

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European Commission approves Elocta for hemophilia A

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European Comission grants two landmark approvals to Novartis' Consentyx

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European Commission gives conditional marketing authorization to Blincyto

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Gilead Sciences' Genvoya approved in E.U. for HIV-1 infection

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