Kelly Davio


Could the United States Invoke the Bayh-Dole Act to Curb Drug Prices?

June 27, 2017

As patients, policy makers, and providers alike wait to learn the fate of the contentious new Senate healthcare bill, some stakeholders suggest that existing legislation—dating back to the 1980s—could potentially play a role in driving down prescription drug costs.

After Patient Pressure, NHS England Strikes Kadcyla Deal With Roche, Wales Follows Suit

June 22, 2017

After negotiations with drug manufacturer Roche, England’s National Health Service (NHS) has approved the routine use of trastuzumab emtansine (Kadcyla) for the treatment of HER2-positive metastatic breast cancer in patients for whom trastuzumab (Herceptin) treatment has failed.

An Expert Discussion: Lessons Learned and the Future of Biosimilar Uptake

June 21, 2017

At the 8th Annual Summit on Biosimilars, a panel of legal experts reviewed lessons learned from the first 18 months of biosimilars in the United States, and looked ahead to the question of how these drugs will gain acceptance and market uptake.

Adding a Biologic to Methotrexate May Benefit Patients With Early RA

June 20, 2017

In a recent study, researchers sought to investigate the clinical impact of 1-year certolizumab pegol therapy added to the first year of a 2-year treatment with methotrexate in patients with early rheumatoid arthritis.

Danish NGO Plays a Key Role in Patient Education on Biosimilars

June 19, 2017

Denmark is the first nation in Europe—and in the world—to switch all well-treated rheumatoid arthritis patients from reference infliximab (Remicade) to the biosimilar Remsima, and 1 early study suggests that the switch has been successful. Patients, however, have needed convincing.

Legal Experts Grapple With Implications of Sandoz v Amgen at the Summit on Biosimilars

June 15, 2017

News of the landmark Supreme Court ruling in the case of Sandoz v Amgen broke during the Monday session of the 8th Annual Summit on Biosimilars, a meeting of legal and pharmaceutical industry professionals convened in New York City. In a previously scheduled—and swiftly updated—discussion of the case, a panel of attorneys grappled with the ruling and its implications for the industry.

Study Finds Significant Differences in Glycemic Control Between Reference and Biosimilar Morning Insulin

June 14, 2017

In order to investigate the best morning insulin therapy to improve glycemic variability in patients with type 2 diabetes, researchers from Japan compared morning injections of insulin glulisine and insulin glargine with injections of insulin lispro and insulin glargine biosimilar.