Wolitz RE - Seton Hall Law Review
States face severe budget pressures from patented brand-name drug costs, with single treatments sometimes exceeding half a billion dollars, forcing difficult trade-offs between medication access and funding for other critical services. The authors examine whether states can implement cost-containment and fair-pricing measures for patented drugs despite patent preemption doctrine, which limits state regulatory authority over federally-granted patent rights.
VIEW SOURCE
Eisenkraft Klein D, Kesselheim AS - Clinical Pharmacology & Therapeutics
Cai CL, Bucha S, Kesselheim AS, Rome BN - Journal of General Internal Medicine
Chen NC, Bullement A, Zemplenyi AT, O'Bryant CL, Kaizer AM, Anderson KE, McQueen RB - PharmacoEconomics Open