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BioWorld - Wednesday, May 6, 2026
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Dimerix's lead compound meets primary endpoints in phase II CKD trial

July 14, 2017
By Tamra Sami
PERTH, Australia – Dimerix Ltd. reported positive phase IIa data with its lead program, DMX-200, in chronic kidney disease.
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Machine learning whole genome analysis may lead to better cancer treatment

July 14, 2017
By Stacy Lawrence
Can machine learning glean useful information from whole genome analysis faster than conventional approaches? And, more crucially, can that help lead to better treatment for cancer patients? A new study published by researchers at the New York Genome Center (NYGC), The Rockefeller University and IBM suggests that the answer to those questions may be yes.
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Industry groups urge Brexit negotiations to include close regulatory ties between U.K., EU

July 13, 2017
By Nuala Moran
LONDON – The biotech and pharma industry across Europe has put its combined firepower behind a new lobbying offensive to keep Europe's medicines regulatory system intact after the U.K. leaves the EU.
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House passes user fee on voice vote

July 13, 2017
By Mark McCarty
Congress rarely scores a bipartisan win these days, so it was with some relish that the House of Representatives gaveled down on a voice vote on H.R. 2430, the bill that reauthorizes the FDA user fee programs for the next five years.
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The great E-Scape? Freed of A-beta, taus that bind, AD ApoE4 protein target

July 13, 2017
By Randy Osborne
Topping off a series A round that began in the summer of 2015 with $55 million, E-Scape Bio Inc. raised $63 million in total that CEO Leon Chen told BioWorld should carry the firm into proof-of-concept work that takes aim at the apolipoprotein E4 (ApoE4) protein structure in Alzheimer's disease (AD).
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VBI takes aim at global HBV market with phase III Sci-B-Vac program

July 13, 2017
By Marie Powers
As promised last year during its merger with Scivac Therapeutics Inc., VBI Vaccines Inc. is seeking to move Sci-B-Vac, a third-generation hepatitis B virus (HBV) vaccine licensed in Israel and 14 other countries, onto the world stage. After gathering input from the FDA, EMA and Health Canada, the Cambridge, Mass.-based company is preparing to conduct a 15-month phase III program that will include two concurrent studies – the safety and immunogenicity PROTECT study and lot-to-lot consistency CONSTANT study – with combined enrollment of approximately 4,800 participants across some 40 sites in the U.S., Europe and Canada.
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FDA speech bills draw partisan lines in House hearing

July 13, 2017
By Mark McCarty
A hearing in the U.S. House of Representatives dealing with FDA regulation of commercial speech highlighted the partisan nature of this issue, but the Republican majority in the House and the FDA's inability to come to terms with the First Amendment suggest that support for the two bills in question will continue to build, particularly given that patient advocates at the hearing had few kind words for the legal and regulatory status quo.
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Measuring 'watery fat' improves value of CT readouts

July 13, 2017
By Anette Breindl
A new way of analyzing computerized tomography (CT) angiography, the standard method for imaging blood vessels to look for potential blockages, could help find future trouble spots before they are causing trouble.
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Financings

July 13, 2017
Egalet Corp., of Wayne, Pa., said it closed its underwritten public offering of 16.66 million shares of its common stock and accompanying warrants to purchase up to 16.66 million shares, at a combined public offering price of $1.80 per share and accompanying warrant. The gross proceeds are expected to be approximately $30 million. The company anticipates using the net proceeds to support its commercial sales and marketing efforts for Arymo ER (morphine sulfate) extended-release tablets for oral use - CII, Sprix (ketorolac tromethamine) nasal spray and Oxaydo (oxycodone HCI, USP) tablets for oral use only CII, and for general corporate purposes. Cantor Fitzgerald & Co. acted as the sole book-running manager.
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Other news to note

July 13, 2017
Applied Immunotherapeutics Inc., of Morris, Conn., and The Feinstein Institute for Medical Research at Northwell Health inked a deal in which Applied licensed discoveries in treating inflammation, as well as specific antibodies and drug candidates. Included in the agreement are patent rights covering the use of antibody and small-molecule therapeutics against HMGB1, an established target in inflammatory and autoimmune diseases. Terms were not disclosed.
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