New Rule Might Increase Out-of-Pocket Drug Costs for Patients
Patients may face increased out-of-pocket drug costs as a result of a rule finalized by the Centers for Medicare & Medicaid Services in July 2020.

Patients may face increased out-of-pocket drug costs as a result of a rule finalized by the Centers for Medicare & Medicaid Services in July 2020.
Three developments may have effects on the use of patents to fend off competition for therapeutic monoclonal antibodies.
The purpose of the secondary patent filings was to assemble a thicket of patents, 132 in all, to prohibit competition from biosimilar companies.
Selections feature topics ranging from political pressures facing the FDA, to the financial incentive structure for antibiotic development.
Interesting empirical studies, policy analyses, and editorials on pharma, health law, and policy issues from August 2020.
A recent executive order aimed at addressing ballooning pharmaceutical expenditures is ambitious in scope, but its impact remains to be seen.
Interesting empirical studies, policy analyses, and editorials on health law and policy issues from July 2020.
While generic competition is crucial for reducing drug prices, brand-name drug manufacturers can utilize several strategies to delay such competition.
A positive outcome of the pandemic may be the demonstration via emergency measures that state governments can be flexible in substitution policies.
By Ameet Sarpatwari, Charlie Lee, Frazer Tessema, and Aaron S. Kesselheim Each month, members of the Program On Regulation, Therapeutics, And Law (PORTAL) review the peer-reviewed medical literature to identify interesting empirical studies, policy analyses, and editorials on health law and policy issues relevant to current or potential future work in the Division.