Early and unrestricted access to high-efficacy disease-modifying therapies: a consensus to optimize benefits for people living with multiple sclerosis

Altres autors/es

Institut Català de la Salut

[Filippi M] Neurology Unit, Neurorehabilitation Unit, Neurophysiology Service, and Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Rafaele Scientifc Institute, 20132 Milan, Italy. Vita-Salute San Rafaele University, Milan, Italy. [Danesi R] University of Pisa, Pisa, Italy. [Derfuss T] University of Basel, Basel, Switzerland. [Duddy M] The Newcastle Upon Tyne Hospitals, Newcastle upon Tyne, UK. [Gallo P] University of Padua, Padua, Italy. [Gold R ] Ruhr-Universität Bochum, Bochum, Germany. [Tintoré M] Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Data de publicació

2022-07-19T10:31:18Z

2022-07-19T10:31:18Z

2021

2022-03



Resum

Healthcare system; Multiple sclerosis; Pharmacoeconomics


Sistema de atención de la salud; Esclerosis múltiple; Farmacoeconomía


Sistema d'atenció de la salut; Esclerosi múltiple; Farmacoeconomia


Early intervention with high-efficacy disease-modifying therapy (HE DMT) may be the best strategy to delay irreversible neurological damage and progression of multiple sclerosis (MS). In European healthcare systems, however, patient access to HE DMTs in MS is often restricted to later stages of the disease due to restrictions in reimbursement despite broader regulatory labels. Although not every patient should be treated with HE DMTs at the initial stages of the disease, early and unrestricted access to HE DMTs with a positive benefit–risk profile and a reasonable value proposition will provide the freedom of choice for an appropriate treatment based on a shared decision between expert physicians and patients. This will further optimize outcomes and facilitate efficient resource allocation and sustainability in healthcare systems and society.


Novartis facilitated two advisory boards on ‘Unrestricted access for RMS therapy and optimal patient outcome’ with physicians, health economists and patient groups to collect insights on the access to MS therapies across Europe as well as on the therapeutic strategy in MS with high efficacy early. These insights contributed to the manuscript content, which was then suggested for publication on a voluntary basis by the experts who wished to be authors. The content is owned and driven by the authors. The Sponsor had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Tipus de document

Article


Versió publicada

Llengua

Anglès

Publicat per

Springer

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http://creativecommons.org/licenses/by/4.0/

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