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BioWorld - Saturday, April 11, 2026
Home » Authors » Mari Serebrov

Articles by Mari Serebrov

Biotech Foundations: Aeras Takes on the World of Tuberculosis Prevention

May 19, 2011
By Mari Serebrov
Global in perspective, Aeras, a nonprofit product development partnership (PDP), is singular in its focus – developing the first new preventive tuberculosis (TB) vaccines in nearly a century.
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NewCo News: RxBio Works on Bridge from NIAID to BARDA

May 18, 2011
By Mari Serebrov
RxBio Inc. has been hard at work building the funding bridge it's counting on to take its lead candidate, RX100, down the home stretch toward approval.
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Head Start Gives Merck's Victrelis Little Advantage

May 17, 2011
By Mari Serebrov
News of Friday's FDA approval of Merck & Co. Inc.'s Victrelis as the first new hepatitis C drug in more than a decade is being overshadowed by the impending approval of the next in line, Vertex Pharmaceutical Inc.'s Incivek.
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The Public ROI from Drug Prices

May 16, 2011
By Mari Serebrov
Biopharma is often the scapegoat for the escalating cost of healthcare, especially when it comes to the price of brand drugs. But since it’s hard to put a price on health and a long life, what gets lost in this focus on the bottom line is the public return on investment (ROI). National Institutes of Health (NIH) Director Francis Collins made that case last week when he testified before a Senate appropriations subcommittee. “Due in large measure to NIH research [and better treatment], our nation has gained about one year of longevity every six years since 1990,” he said. But...
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Another Stopgap May be Needed to Keep SBIR Funded

May 16, 2011
By Mari Serebrov
WASHINGTON – As the clock ticks down on the May 31 expiration of the Small Business Innovation Research (SBIR) program, the Senate is considering yet another continuing resolution to keep the program running while Congress tries to hammer out the details of a multiyear reauthorization.
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Merck's Hepatitis C Drug Gets FDA Approval

May 16, 2011
By Mari Serebrov
WASHINGTON – The FDA approved Merck & Co. Inc.'s Victrelis Friday as the first new chronic hepatitis C treatment in more than a decade.
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Is CER the Rx for Personalized Medicine?

May 16, 2011
By Mari Serebrov

Japanese Biopharmas Put Price Tag on Tsunami Damages

May 11, 2011
By Mari Serebrov
In the two months since the 9.0 Tohoku earthquake triggered a massive tsunami that ravaged much of Japan's eastern coast, several of the country's biopharmaceutical companies have worked around the clock to assess the damages and get their facilities back into production despite power outages and crippled infrastructure.
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FDA Tweaks PDUFA for Biosimilar User Fees

May 10, 2011
By Mari Serebrov
WASHINGTON – The FDA sees a $150,000 annual biosimilar product development fee as the solution to a unique challenge posed by the new 351(k) approval path.
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Biopharma Policies Land Trade Partners on Watch List

May 9, 2011
By Mari Serebrov
WASHINGTON – Tangled webs of regulatory requirements and a murky lack of transparency are keeping several countries on the U.S. Trade Representative's (USTR) list of trade partners that bear watching when it comes to opening the door to American biopharmaceuticals and protecting their patents.
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