Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Mark R, Trusheim"'
Publikováno v:
Drug Discovery Today. 27:17-30
Durable cell and gene therapies potentially transform patient lives, but payers fear unsustainable costs arising from the more than 1000 therapies in the development pipeline. A novel multi-module Markov chain Monte Carlo-based model projects product
Autor:
Zeid El-Kilani, Jacqueline L. Chen, Ernst R. Berndt, Mark R. Trusheim, Ariel Dora Stern, Amber Jessup, Melissa Ouellet
Publikováno v:
Health Affairs. 40:989-999
Biologic drugs account for a disproportionate share of the increase in pharmaceutical spending in the US and worldwide. Against this backdrop, many look to the expanding market for biosimilars—foll...
Publikováno v:
New England Journal of Medicine. 382:473-480
Rewards of Successful Drug Development Risks and rewards change during the life cycle of a drug. In the innovation period, drug companies invest in developing new products but cannot sell them. New...
Autor:
Ariel D, Stern, Mark R, Trusheim
Publikováno v:
Health affairs (Project Hope). 40(9)
Autor:
Ariel Dora, Stern, Jacqueline L, Chen, Melissa, Ouellet, Mark R, Trusheim, Zeid, El-Kilani, Amber, Jessup, Ernst R, Berndt
Publikováno v:
Health affairs (Project Hope). 40(6)
Biologic drugs account for a disproportionate share of the increase in pharmaceutical spending in the US and worldwide. Against this backdrop, many look to the expanding market for biosimilars-follow-on products to biologic drugs-as a vehicle for con
Autor:
Kenneth A. Oye, Kenneth I. Kaitin, Newell E. McElwee, Heather C. Kaplan, Ralph B. D'Agostino, Richard L. Kravitz, Kay Larholt, Hans Georg Eichler, Willard H. Dere, Chandra Ramanathan, S. Nassir Ghaemi, Mark R. Trusheim, Eleanor M. Perfetto, Vicki L. Seyfert-Margolis, Marisha E. Palm, Theodora Cohen, Christopher H. Schmid, Peter Honig, Harry P. Selker
Publikováno v:
Clinical pharmacology and therapeutics. 112(2)
Clinicians and patients often try a treatment for an initial period to inform longer-term therapeutic decisions. A more rigorous approach involves N-of-1 trials. In these single-patient crossover trials, typically conducted in patients with chronic c
Autor:
David Strutton, Kay Larholt, Brigitte Schwarzer-Daum, Martin Brunninger, Gigi Hirsch, Markus Zeitlinger, Mark R. Trusheim, Hans-Georg Eichler, Michael Y. Sherman
Publikováno v:
Clinical pharmacology and therapeutics. 111(1)
Basic scientists and drug developers are accelerating innovations toward the goal of precision medicine. Regulators create pathways for timely patient access to precision medicines, including individualized therapies. Healthcare payors acknowledge th
Autor:
Mondher Toumi, Hilde Stevens, Sissel Michelsen, Isabelle Huys, Eline van Overbeeke, Steven Simoens, Mark R. Trusheim
Publikováno v:
Drug discovery today
This review can inform gene therapy developers on challenges that can be encountered when seeking market access. Moreover, it provides an overview of trends among challenges and potential solutions.
SCOPUS: re.j
info:eu-repo/semantics/publi
SCOPUS: re.j
info:eu-repo/semantics/publi
Publikováno v:
International Journal of Technology Assessment in Health Care. 34:163-171
Objectives: Value assessment frameworks have gained prominence recently in the context of U.S. healthcare. Such frameworks set out a series of factors that are considered in funding decisions. The UK's National Institute of Health and Care Excellence
Autor:
Mark R. Trusheim, Ariel Dora Stern
Publikováno v:
Health Affairs. 40:1516-1516