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BioWorld - Tuesday, March 17, 2026
Home » Authors » Marie Powers

Articles by Marie Powers

Atlas-backed Avrobio lands $25M series A for ex-vivo gene therapy

Aug. 3, 2016
By Marie Powers
After seeding gene therapy start-up Avrobio Inc. earlier this year, Atlas Venture stepped back up to the plate, joined by Clarus and SV Life Sciences, to fund the company’s $25 million series A. The round will accelerate development of Avrobio’s initial programs in Fabry disease and acute myeloid leukemia (AML), both expected to enter the clinic this year, and allow the company to expand its pipeline in rare diseases and solid and liquid cancers.
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Pfizer plucks Bamboo Therapeutics, rAAV tech in potential $645M gene therapy play

Aug. 2, 2016
By Marie Powers
Bamboo is the largest and one of the fastest growing members of the grass family, with individual shoots reaching their full height in a single growing season. In an apt metaphor, Pfizer Inc. made quick work of privately held Bamboo Therapeutics Inc., paying $150 million up front and committing to milestone payments of up to $495 million just months after investing $43 million for a 22 percent equity stake in the Chapel Hill, N.C.-based company.
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As big pharma reports earnings, is it a big deal or no deal?

Aug. 1, 2016
By Marie Powers
Second-quarter earnings season wrapped up for big pharma with a sales miss by Sanofi SA as it sought to modify its tactical pursuit of Medivation Inc., which reports its financial results after the market close on Aug. 9.
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Biopharma looks to big data for the next big breakthrough

July 29, 2016
By Marie Powers

The big data revolution is all around us, from politics to power plants, manufacturing to multimedia content, Wall street to Main Street. Small wonder that big data also is driving radical change in health care and therapeutic development.


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Biomarin serves up ‘bloody good data’ on BMN 270 hemophilia A gene therapy

July 29, 2016
By Marie Powers
Interim results from the open-label phase I/II study of BMN 270, Biomarin Pharmaceutical Inc.’s gene therapy to treat severe hemophilia A, showed the candidate outperformed expectations both in terms of efficacy, as measured by factor VIII (fVIII) expression and clinical improvements.
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Street to Gilead: Hurry up already on dealmaking front

July 27, 2016
By Marie Powers
Disappointing second-quarter earnings at Gilead Sciences Inc. forced shares (NASDAQ:GILD) down 8.5 percent Tuesday, closing at $81.05 for a loss of $7.50, and led to a chorus of calls for the company to pull the trigger on a big deal.
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Success times three as Tricida team pulls down $55M series C

July 26, 2016
By Marie Powers
Tricida Inc. raised a $55 million series C to support continued development of its chronic kidney disease (CKD) compound, TRC101. The round propelled the South San Francisco-based biopharma to $95 million in funding since its founding in 2014 and positioned it to complete a phase I/II proof-of-concept study for TRC101 and prepare for a type B meeting with the FDA this year.
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Turnover at the top the big surprise as Biogen reports solid quarter

July 22, 2016
By Marie Powers
Biogen Inc. reported solid second-quarter financial results, including revenues of $2.9 billion – a 12 percent increase compared to the same period in 2015. The bigger news – at least to those outside its Cambridge, Mass., headquarters – was the revelation by CEO George Scangos at the outset of the company's earnings call that he will leave the company "sometime within the next few months," following "an orderly transition," to return to the West Coast, spend more time with family and "take on one more set of activities."
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Zafgen punts to follow-on MetAP2 candidate after beloranib bust

July 21, 2016
By Marie Powers
Zafgen Inc. scrapped plans to develop its lead candidate, beloranib, after deciding the road forward would be too long and costly, based on FDA feedback, following two patient deaths in its phase III bestPWS trial in Prader-Willi syndrome (PWS).
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DODAC members size up suicide risk, side with brodalumab

July 20, 2016
By Marie Powers
In a solid win for Valeant Pharmaceuticals International Inc., the FDA's Dermatologic and Ophthalmic Drugs Advisory Committee (DODAC) voted 18-0 in favor of approving the biologics license application (BLA) for brodalumab, branded Siliq, to treat adults with moderate to severe plaque psoriasis.
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