
MUSCULAR DYSTROPHY GROUP OF GREAT BRITAIN AND NORTHERN IRELAND
MUSCULAR DYSTROPHY GROUP OF GREAT BRITAIN AND NORTHERN IRELAND
1 Projects, page 1 of 1
Open Access Mandate for Publications assignment_turned_in Project2016 - 2022Partners:UMC, ERASMUS MC, AstraZeneca (Sweden), ACTELION PHARMACEUTICALS LTD, YAMANOUCHI EUROPE BROCADES PHARMA +33 partnersUMC,ERASMUS MC,AstraZeneca (Sweden),ACTELION PHARMACEUTICALS LTD,YAMANOUCHI EUROPE BROCADES PHARMA,MSD,AMGEN LIMITED,TAK,FEDERAAL KENNISCENTRUM VOOR DE GEZONDHEIDSZORG FODERALES EXPERTISEZENTRUM DES GESUNDHEIT,Newcastle University,EUROPEAN PATIENTS FORUM,CSL BEHRING GMBH,Janssen (Belgium),Uppsala University,AbbVie,NOVARTIS,Bayer Pharma AG,Roche (Switzerland),IAPO,MINDBYTES,SARD,Johnson & Johnson (United States),MUSCULAR DYSTROPHY GROUP OF GREAT BRITAIN AND NORTHERN IRELAND,IEO,University of Birmingham,COLLABORATE PROJECT MANAGEMENT UG HAFTUNGSBESCHRANKT,IRCCS-BARI,Universitätsklinikum Erlangen,KUL,PFIZER,EUR,Bayer AG,IRCCS,TAKEDA,MERCK KOMMANDITGESELLSCHAFT AUF AKTIEN,EUROPEAN PATIENTS FORUM (EPF),ECPC,Eli Lilly and Company LimitedFunder: European Commission Project Code: 115966Overall Budget: 12,015,500 EURFunder Contribution: 6,000,000 EURThe PREFER project will deliver an overview and evaluation of preference elicitation methods to be applied in the entire drug life cycle, i.e. in the early stages of identifying medical needs, in clinical testing, to guide decisions on reimbursement and to make decisions on withdrawal of drugs from the market. A broad array of (combinations of) patient preference methods will be tested prospectively in a large number of case studies. The availability of large patient cohorts will enable to test new methods or deviations from existing methods in a randomized manner, by comparing well-known methods with newer ones. The use of simulation studies will both contribute to smarter design of case studies and to exploring the sensitivity of outcomes of preference studies. Based on discussions with a broad representation of stakeholders e.g. patients, patient organisations, regulatory authorities, HTA bodies and reimbursement agencies, suitable methods will be tested and their contributions to improved decision making will be discussed in recommendations adapted to the needs of all relevant stakeholders. The recommendations from PREFER are expected to lead to changed practices, in that industry will routinely assess whether a preference study would add value at key decision points in the medicinal product life cycle and, if so, implement patient-preference elicitation studies according to the PREFER project recommendations. The PREFER consortium consist of 16 industry partners and 16 academic and SME members including representation from academia, patient organizations, HTA bodies, reimbursement agencies, and project management.
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