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Home » Newsletters » BioWorld Science

BioWorld Science

Nov. 30, 2020

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Enrollment ongoing in phase I/II study of HPN-328 in advanced cancer

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Initiation of phase I/II study of NGM-621 as therapy in patients with SARS-CoV-2 infection

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First-in-human data for the personalized multitarget adoptive cell therapy ACTolog

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Researchers develop a novel murine model of deer tick virus infection

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FDA approves Imcivree as first-ever therapy for POMC, PCSK1 or LEPR deficiency obesities

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Cabometyx approved in Japan for unresectable previously treated HCC

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SmartPharm awarded contract for development of gene-encoded antibody against COVID-19

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Results of a phase Ib trial evaluating the microR-132 inhibitor CDR-132L in heart failure

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VBI Vaccines presents data from part B of ongoing phase I/IIa study of VBI-1901

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CVI Pharmaceuticals details preclinical and first-in-human data for CVI-LM001

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Pelareorep plus GM-CSF shows efficacy, safety and tolerability in ReoGlio study

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ST6GAL1 as serum marker to identify HCC patients who may benefit from lenvatinib therapy

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University of Bern, Silence Therapeutics describe nucleic acids inhibiting PROS1

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COLCORONA trial of colchicine in COVID-19 recommended to continue enrollment

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Janssen discovers anti-HBV compounds

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New CD134 agonists identified at Bicycle Therapeutics

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Eisai and Wren Therapeutics collaborate to target alpha-synuclein to treat synucleinopathies

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Qilu Regor Therapeutics presents new CDK inhibitors

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New EZH2 inhibitors synthesized at PharmaBlock Sciences

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DAY-101 well tolerated, shows antitumor activity in patients with recurrent low-grade glioma

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Phase III study of NC-6004 in pancreatic cancer concludes

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European Commission approves Dupixent for severe atopic dermatitis in children aged 6-11 years

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Novel potent and selective thyroid hormone receptor beta agonists as therapeutic agents in NASH

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New PDE4 inhibitor shows preclinical antifibrotic effect by inhibiting lung macrophage activity

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Hookipa reports interim phase II data on prophylactic CMV vaccine candidate HB-101

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Japan first to approve Humira for pyoderma gangrenosum

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Moderna to file for EUA of mRNA-1273 for COVID-19 following primary efficacy analysis

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