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- W252825564 abstract "These days, there is a lot of press and activity surrounding the implementation of the Medicare prescription drug benefit (Part D) on Jan. 1, 2006. Final regulations, bid applications for sponsors, formulary-design decisions, and outreach and enrollment issues — to name just a few — need to be addressed in an extremely compressed time frame this year. A key question is whether Medicare beneficiary enrollment will be significant. Robust enrollment is desirable for all stakeholders, especially those who wish to take part in the program; the more successful Part D is, the more likely that the program will continue.Many people are pointing to the Medicare Drug Discount Card Program, which was implemented last June, as a benchmark. Enrollment in that program has lagged, despite multiple efforts by the Centers for Medicare and Medicaid Services. Perhaps, a more appropriate example is the current demonstration program designed to mimic many aspects — most importantly, the beneficiary cost-sharing design — of the standard Part D benefit.The demonstration program, known as the Medicare Replacement Drug Demonstration, or MRDD, has been largely ignored due to its relatively small scope of coverage (see table on page 25). Many lessons have been learned, however, and the program continues to provide valuable insight relative to the pending implementation of Part D.TABLEDrugs covered under the Medicare Replacement Drug Demonstration (Updated Feb. 7, 2005)In this article, we will provide some background on the MRDD and share our experience as it relates to one of Amgen’s products (etanercept [Enbrel1], a tumor necrosis factor [TNF] inhibitor) and some of the lessons that have been learned." @default.
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- W252825564 date "2005-02-01" @default.
- W252825564 modified "2023-09-23" @default.
- W252825564 title "Preventing drug coverage disruption for enrollees in the replacement drug demo." @default.
- W252825564 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3564360" @default.
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