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BioWorld - Saturday, March 28, 2026
Home » Newsletters » BioWorld

BioWorld

July 1, 2015

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In the clinic

DBV Technologies SA, of Bagneux, France, disclosed the completion of phase I or part A of the Viaskin Milk Efficacy and Safety phase I/II study known as Miles. Read More

Other news to note

Advanced Accelerator Applications SA (AAA), of Saint-Genis-Pouilly, France, signed a distribution agreement for Lutathera (lutate; 177Lutetium DOTA0 Tyr3-Octreotate) in Japan with Fujifilm RI Pharma Co. Ltd., of Tokyo. Read More

Stock movers

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Financings

PDL Biopharma Inc., of Incline Village, Nev., said it entered a credit agreement with Careview Communications Inc. to provide the firm with up to $40 million of secured debt financing in two tranches of $20 million, based upon the achievement of specified milestones. Read More

Inhibitor discovery offers promising new anticoagulant

HONG KONG – Chinese researchers have discovered a novel nonasaccharide molecule – a nine-unit sugar chain – with potent anticoagulant activity that could avoid adverse effects, paving the way for the development of better treatments for thromboembolic diseases, they reported in the June 22, 2015, early online issue of Proceedings of the National Academy of Sciences. Read More

Annual Hajj points to untapped, growing halal vaccines market

HONG KONG – Before they travel to Mecca every year for the Hajj, an annual pilgrimage, millions of Muslims have to be vaccinated. Read More

Broad-scope epitopes: Influenza phase II data push a step Biondvax

With a progressive strategy that's "building an ecosystem," Biondvax Pharmaceuticals Ltd. offered upbeat preliminary results from the BVX-006 phase II trial gauging the worth of M-001 in the Ness Ziona, Israel-based firm's quest for a universal influenza vaccine, and analyst Ashok Kumar at Aegis Capital Corp. tagged what could be alluring prospects for would-be partners or buyers of the firm. Read More

Solid 'Opera' performance for ocrelizumab; Roche plans 2016 filing in MS

Roche AG is planning early 2016 regulatory filings to seek approvals for ocrelizumab, a twice-yearly injectable multiple sclerosis (MS) therapy, after two phase III studies showed that it significantly reduced relapses and disability progression vs. Rebif (beta interferon 1a, EMD Serono Inc. and Pfizer Inc.) for people with relapsing MS, the most common form of the disease. Read More

FDA is expecting a steady flow of biosimilar applications

Biosimilars in the U.S. are far from the standard fare they're becoming in some countries, but the FDA expects them to be a steady portion of its workload. Read More

CBMG acquires CD40LGVAX vaccine, will test in combo PD-1 trial for NSCLC

SHANGHAI – Shanghai's Cellular Biomedicine Group Inc. (CBMG) has added a cancer vaccine to its pipeline, a Gvax vaccine it intends to combine with a PD-1 drug in a U.S. phase II study for non-small-cell lung cancer (NSCLC). Read More

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