Published by Erik Greb on November 9, 2009
under Biotech, Manufacturing, North America News, Regulation, Trends
After much ado, the US House of Representatives passed a healthcare-reform bill this weekend. Drugmakers and commentators are understandably eager to parse the bill to find out what it would mean for the pharmaceutical and biopharmaceutical industries. So what’s the verdict? Read more »
Published by Erik Greb on November 2, 2009
under Latin & South America News, Manufacturing, Regulation
The pharmaceutical and biopharmaceutical industries have jealously guarded their intellectual property for years. Companies routinely use patents to prevent competitors from making generic versions of their drugs. When pipelines have weakened, companies have developed new formulations or delivery methods to extend patent protection for their established drugs. The economic crisis has only sharpened this reflex.
That’s why news from Ecuador made me do a doubletake. Read more »
Published by Erik Greb on October 12, 2009
under Biotech, North America News, R&D
The pace of progress in stem-cell research seems to be quickening, and the field’s future looks promising. Last week, a team at the Harvard Stem Cell Institute found what looks like a revolutionary way to create stem cells that could be safe enough to use as treatments in humans. Read more »
Published by Erik Greb on October 5, 2009
under Biotech, Drug Delivery, R&D, Trends
When pipelines run dry, pharmaceutical companies are more likely to investigate alternative delivery methods as a way of distinguishing their drugs in the marketplace. In the past few weeks, I’ve noticed several intriguing delivery methods created by researchers around the world. I recently wrote about the new technique of encapsulating medicines in magnetite nanoparticles for repeated, long-term delivery. Along similar lines, scientists at Queen Mary, University of London have created “micro shuttles” that can be loaded with drugs and opened remotely. Read more »
Published by Erik Greb on September 21, 2009
under Biotech, Drug Delivery, Formulation, Manufacturing, North America News, R&D, Trends
Last week, I wrote that the increased attention to biological drugs, which are mostly taken through injections, was spurring interest in needle-free and implantable delivery methods for vaccines. Research into alternative delivery methods for vaccines could produce innovative ways of delivering other kinds of drugs as well, and I recently read about an inspired idea that a team of Boston researchers had for delivering intermittent doses of drugs. Read more »
Published by Erik Greb on September 14, 2009
under Biotech, Drug Delivery, Formulation, Manufacturing, R&D, Trends
Have you ever considered getting a flu shot but quailed at the sight of the needle? Lots of people hate getting injections, but this delivery method is still the predominant technique for administering biological drugs. Rising demand for vaccines and other biologicals is one factor spurring manufacturers to seek alternative delivery methods that could one day rescue the needlephobic. Read more »
Published by Erik Greb on August 24, 2009
under Biotech, Manufacturing, North America News, Regulation
Two announcements made on two consecutive days last week vividly showed that whether a thing is helpful or harmful often depends on how we use it. The announcements’ subject? Tobacco. Read more »
Published by Erik Greb on August 10, 2009
under Biotech, Manufacturing, North America News, R&D, Regulation
Last Thursday, the Biotechnology Industry Organization (BIO) weighed in on a patent issue that will soon be before the Supreme Court. In an amicus brief, BIO argued that the Court should overturn Bilski v. Doll, a decision of the US Court of Appeals for the Federal Circuit. The case involved Bernard L. Bilski’s method for hedging risks in commodities trading. Read more »
Published by Erik Greb on August 3, 2009
under Biotech, Manufacturing, North America News, Regulation
The Biotechnology Industry Organization (BIO) has won the latest battle over follow-on biologics. Last week, the House Energy and Commerce Committee approved Rep. Anna Eshoo’s (D-CA) amendment to the America’s Affordable Health Choices Act (H.R. 3200). The Eshoo amendment, a regulatory pathway for the approval of biosimilars, would grant about 12 years of market exclusivity to each new biological medicine. Read more »
Published by Erik Greb on July 27, 2009
under Asia News, Europe News, Manufacturing, Trends
Reading the news sometimes gives me a disorienting sense of déjà vu. I know I wrote that last week, but it’s true again for a different reason. Today, French heavyweight sanofi aventis (Paris) announced that it was acquiring a majority stake in Shantha Biotechnics (Hyderabad, India). This new development follows a now-familiar pattern. Read more »
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