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BioWorld - Sunday, March 1, 2026
Home » Authors » Marie Powers

Marie Powers

Articles

ARTICLES

Rear-View Mirror Offers Preview of Road Forward

April 22, 2013
By Marie Powers
CHICAGO – The BIO International Convention is celebrating 20 years in 2013, and in some ways everything old is new again.
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ActoGeniX Series B to Move IBD Program to IND Stage

April 19, 2013
By Marie Powers
ActoGeniX NV closed a Series B equity financing round, raising €10.7 million (US$14 million) to move its ActoBiotics program to the investigational new drug application (IND) stage in a second indication of inflammatory bowel disease (IBD).
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FDA Stalls on Accelerated Nod, Seeks More Data on Eteplirsen

April 17, 2013
By Marie Powers
Sarepta Therapeutics Inc. disclosed Monday afternoon following the market's close that the FDA has asked for additional information from its existing eteplirsen dataset before making a determination about a new drug application (NDA) filing for the drug under Subpart H accelerated approval.
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Portola Joins IPO Parade, Seeks $115M for Thrombosis Portfolio

April 16, 2013
By Marie Powers
Portola Pharmaceuticals Inc. became the 12th biotech in 2013 and the third in the second quarter seeking to move into the U.S. public markets, filing an S-1 with the SEC for an initial public offering (IPO). The company did not disclose the number of shares or price range.
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Beware the 'simple' path: combo drug/devices tricky

April 15, 2013
By Marie Powers

Armetheon Seeks to Repurpose Stalled Late-Stage Compounds

April 15, 2013
By Marie Powers
Privately held Armetheon Inc. was launched in October 2011 with a mission to create novel antibiotics for drug-resistant bacteria. However, that program quickly took a back seat when the founders discovered a new use for a compound, tecarfarin, advanced by another biotech where several of them had played leading roles.
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Beware the 'Simple' Path: Combo Drug/Devices Tricky

April 12, 2013
By Marie Powers
Pity the poor drug developer that thinks using the combination drug/device regulatory pathway through the FDA's Office of Combination Products (OCP) could be a shortcut to approval, bypassing the sometimes unpredictable regulatory oversight of the Center for Drug Evaluation and Research (CDER) or the Center for Biologics Evaluation and Research (CBER).
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Ambrx Lands Another Pharma In Potential $300M Astellas Deal

April 8, 2013
By Marie Powers
Privately held Ambrx Inc. gained another partner for one of its signature technologies, attracting Tokyo-based Astellas Pharma Inc. to an oncology-focused discovery and development collaboration in antibody drug conjugates (ADCs).
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Topical HDAC Inhibitor Could 'Shape' CTCL Care

April 5, 2013
By Marie Powers
Shape Pharmaceuticals Inc. is not aiming to reshape the industry. The Cambridge, Mass.-based biotech has the more modest goal of advancing its single asset, topical histone deacetylase (HDAC) inhibitor SHP-141, in cutaneous T-cell lymphoma (CTCL) and, potentially, other inflammatory skin conditions.
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Geron ESC Assets Regenerate at Asterias Biotherapeutics

April 4, 2013
By Marie Powers
A 300-page S-1 filing with the SEC on Wednesday revealed that Geron Corp.'s human embryonic stem cell (ESC) assets, left dangling when the company abandoned the field in late 2011, will be reborn at Asterias Biotherapeutics Inc., a newly formed subsidiary of regenerative medicine specialist BioTime Inc.
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