PHARMACY

Iluvien aids patients with diabetic macular edema, trial concludes

BY Alaric DeArment

WATERTOWN, Mass. More than half the patients taking the low dose of a drug for diabetic macular edema were able to read at least five additional letters on a vision chart two years after beginning therapy with the drug, according to late-stage clinical results presented at the Angiogenesis 2010 meeting in Miami.

Data from FAME, a phase 3 study of pSivida Corp.’s drug Iluvien (fluocinolone acetonide) included efficacy and safety data in addition to results presented in December 2009 by pSivida and its licensee, Alimera Sciences. The study also showed that 28.7% of DME patients taking a low dose of the drug and 28.6% of those taking a high dose were able to see 15 additional letters, compared with 16.2% of those in the control group.

“We are very encouraged by the additional data presented at the Angiogenesis 2010 meeting and look forward to the upcoming NDA filing for potentially the first ophthalmic drug therapy approved for DME,” pSivida president and CEO Paul Ashton said in a statement.

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FDA approves extended-release painkiller

BY Alaric DeArment

CAMBRIDGE, Mass. The Food and Drug Administration has approved a regulatory approval application for a pain drug made by CombinatoRx, the drug maker announced Tuesday.

The FDA approved Exalgo (hydromorphone hydrochloride) extended-release tablets, for the management of moderate to severe pain in patients who need continuous pain relief for long periods of time.

Covidien will pay CombinatoRx a $40 million milestone payment for the approval and is eligible to receive tiered royalties on sales of the drug.

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Surescripts: E-prescription use jumps 181%

BY Allison Cerra

ALEXANDRIA, Va. E-prescription adoption and use in the United States has skyrocketed over the past two years, according to a new report developed by an e-prescription network.

Surescripts, which announced the release of its 2009 national progress report on e-prescribing titled “Advancing Healthcare in America,” measures the growth of e-prescribing from 2007 through 2009 across a number of categories. Among the key findings: E-prescription use increased 181%, from 68 million in 2008 to 191 million e-prescriptions in 2009.

Additional findings included:

  • Prescription Benefit Information: The number of electronic requests for prescription benefit information more than tripled, from 79 million in 2008 to 303 million in 2009
  • Prescription History Information: The number of prescription histories delivered to prescribers grew more than five-fold, from 16 million in 2008 to 81 million in 2009
  • Prescribers: The number of prescribers routing prescriptions electronically grew from 74,000 at the end of 2008 to 156,000 by the end of2009 — representing 25 percent of all office-based prescribers
  • Pharmacies: At the end of 2009, approximately 85% of community pharmacies and six of the largest mail-order pharmacies in the United States were able to receive prescriptions electronically

Surescripts president and CEO Harry Totonis said the report emphasizes the benefits of e-prescribing.

“For e-prescription use to jump from 6% to 18% in one year indicates several things,” said Harry Totonis, president and CEO of Surescripts. “First, that the federal government’s leadership and incentive structures are working. Second, that the benefits of e-prescribing — including increased safety, lower costs and increased efficiency — are widely understood. And last, that the nation’s experience with e-prescribing — in building the network and the ecosystem to support it — provides a definitive road map for how to drive adoption of a broader electronic health record for all Americans.”

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