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BioWorld - Sunday, December 7, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

June 25, 2019

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Gold nanoparticles found to improve CRISPR delivery system for gene editing

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DGM1 as a novel biomarker of response to enzastaurin in DLBCL and glioblastoma

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ROCK inhibition suppresses tumorigenesis in resistant CSCs

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Phase I/IIa trial of gB/pp65 CMV immunotherapeutic vaccine in recurrent glioblastoma

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FDA approves sBLA for Botox for pediatric patients with upper limb spasticity

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'Cheap and straightforward' structure predictions

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Results presented from first-in-human study of REGN-3767 against advanced malignancies

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Data reported from phase II study of pembrolizumab for recurrent respiratory papillomatosis

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First-in-human results demonstrate [64Cu]/[67Cu] to be a nearly ideal theranostic pair

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Early clinical results reported from trials of anti-CD32b antagonistic antibody BI-1206

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RSLV-132 moves into phase III for Sjogren syndrome after reduced fatigue seen in phase II

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X-Cutag Therapeutics patents new compounds for cancer

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Lin Bioscience synthesizes tubulin polymerization inhibitors

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Epizyme discloses new KAT inhibitors

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Applied Therapeutics initiates phase I/II study of AT-007 in galactosemia

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Dextenza approved by FDA to treat ocular inflammation following ophthalmic surgery

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FDA approves Vyleesi for hypoactive sexual desire disorder in premenopausal women

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Symdeko obtains FDA approval for cystic fibrosis in children aged 6-11 years

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Talzenna approved in E.U. for germline BRCA-mutated locally advanced or metastatic breast cancer

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Kissei Pharmaceutical identifies new CGRP antagonists

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Bayer initiates phase III trial of aflibercept in retinopathy of prematurity

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Oscotec describes new LRRK2 inhibitors

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Axsome enrolls first patient in phase III GEMINI study of AXS-05 for MDD

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FDA allows Athenex's IND to study pegtomarginase for advanced malignancies

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FDA lifts partial clinical hold on phase III CANOVA trial of venetoclax in multiple myeloma

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FDA clears Minerva's IND for huMNC2-CAR44 for metastatic breast cancer

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FDA issues complete response letter for quizartinib in relapsed/refractory FLT3-ITD AML

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