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BioWorld - Sunday, January 18, 2026
Home » Authors » Marie Powers

Marie Powers

Articles

ARTICLES

Despite 'choppy' markets, fundamentals strong as health care world heads to JPM

Jan. 11, 2016
By Marie Powers
SAN FRANCISCO — As investors in biopharma, medtech and affiliated industries descend on San Francisco for the start of the 34th Annual J.P. Morgan Healthcare Conference (JPM), invited guests and throngs of hangers-on could be forgiven for glancing nervously over their shoulders at the global capital markets.
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Despite 'choppy' markets, fundamentals strong as health care world heads to JPM

Jan. 9, 2016
By Marie Powers

As investors in biopharma, medtech and affiliated industries descend on San Francisco for the start of the 34th Annual J.P. Morgan Healthcare Conference (JPM), invited guests and throngs of hangers-on could be forgiven for glancing nervously over their shoulders at the global capital markets. In the wake of geopolitical and macroeconomic uncertainties – currency and stock roiling in China, oil-fueled power brokering in the Middle East, election year politicking in the U.S. and saber-rattling in North Korea – the first trading days of 2016 took investors on a wild ride, and they might need to hold onto their hats for the foreseeable future.


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Petra 'accelerates' into $48M series A to tackle cancer, metabolic disease

Jan. 6, 2016
By Marie Powers
Petra Pharma Corp. became the first life science start-up for the 1-year-old New York arm of Accelerator Corp., initially established more than a dozen years ago in Seattle.
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Scholar 'Rock on' $36M series B shows faith in growth factor activation

Jan. 5, 2016
By Marie Powers
Scholar Rock Inc., the 2-year-old company pursuing drugs that target supracellular activation of growth factors, jump-started its New Year with a $36 million series B financing.
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Translation regulation: $40M series B shifts Effector into clinic mode

Dec. 23, 2015
By Marie Powers
Two years after entering a crowded field seeking to control gene expression in treating cancer, Effector Therapeutics Inc. showed that its approach – the development of small-molecule translation regulators – has staying power by landing a $40 million series B to advance its first two programs into the clinic.
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HIV heats up as BMS pipeline goes to Viiv in multibillion-dollar deal

Dec. 21, 2015
By Marie Powers
Bristol-Myers Squibb Co. (BMS) exited development of HIV therapies in a big way, selling its entire R&D pipeline of HIV assets to erstwhile competitor Viiv Healthcare Ltd., the joint venture established in 2009 by Glaxosmithkline plc and Pfizer Inc. to focus on HIV medicines.
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Velicept feels urge to address OA bladder market with GSK-developed solabegron

Dec. 18, 2015
By Marie Powers
Overactive bladder (OAB) and irritable bowel syndrome (IBS) aren't the sexiest indications in the drug development universe, but tens of millions of patients remain untreated or undertreated for the common, uncomfortable conditions. With that large unmet need in mind, Velicept Therapeutics Inc. recently closed the first tranche of a $21 million series B financing to advance an asset that could potentially address both.
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Astrazeneca sews up global Daliresp rights in $575M Takeda respiratory deal

Dec. 17, 2015
By Marie Powers
Astrazeneca plc expanded its reach in the global respiratory market with a $575 million deal to acquire the core respiratory assets of Takeda Pharmaceutical Co. Ltd. The transaction included the expansion of rights to roflumilast, marketed as Daliresp in the U.S. and Daxas elsewhere, a once-daily oral PDE4 inhibitor approved to treat chronic obstructive pulmonary disease (COPD).
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No pain, big gain: Kitov combo drug shines in phase III trial

Dec. 16, 2015
By Marie Powers
Tiny Kitov Pharmaceuticals Holdings Ltd. made a big splash in the drug development world with news that its lead candidate, KIT-302, met the primary efficacy endpoint of reducing blood pressure as a combo drug that also treats osteoarthritic (OA) pain during a double-blind, placebo-controlled phase III trial that received a special protocol assessment from the FDA.
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Atara confronts ‘the difficult questions,’ axes PINTA 745 after phase II failure

Dec. 15, 2015
By Marie Powers
Atara Biotherapeutics Inc. is suspending development of PINTA 745 after the peptide-antibody combination missed its primary endpoint, defined as percent change from baseline in lean body mass as measured by dual energy X-ray absorptiometry at week 12, in a phase II proof-of-concept study.
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View All Articles by Marie Powers

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