Economic Evaluation of Cladribine Tablets in Patients With High Disease Activity-Relapsing-Remitting Multiple Sclerosis in the Kingdom of Saudi Arabia.


Journal

Value in health regional issues
ISSN: 2212-1102
Titre abrégé: Value Health Reg Issues
Pays: United States
ID NLM: 101592642

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 26 05 2020
revised: 25 02 2021
accepted: 11 03 2021
pubmed: 24 8 2021
medline: 26 11 2021
entrez: 23 8 2021
Statut: ppublish

Résumé

Cladribine tablets are the first short-course oral treatment approved for high disease activity relapsing-remitting multiple sclerosis (HDA-RRMS) across various countries. This analysis assessed the cost-effectiveness of introducing cladribine tablets as a treatment option for patients with high disease activity compared with other HDA-RRMS therapies in the Kingdom of Saudi Arabia (KSA). The cost-effectiveness model was adapted from the KSA payer's perspective. Data for the model's adaptation were retrieved from the literature and validated by key opinion leaders. The comparators considered in the model were alemtuzumab, dimethyl fumarate, fingolimod, interferon beta-1a (subcutaneous and intramuscular) and beta-1b, natalizumab, and teriflunomide. A sensitivity analysis was also performed to assess the robustness of the analysis. The cost-effectiveness results showed cladribine tablets as the dominant strategy (ie, less costly and more effective) versus all the comparators. The incremental cost and quality-adjusted life-years gained were largely driven by drug acquisition cost and delayed expanded disability status scale progression, respectively. Cladribine tablets showed an 81% to 100% probability of being cost-effective at a threshold of Saudi Riyal 225 326 per quality-adjusted life-years gained against different comparators. Cladribine tablets are a dominant treatment option for patients with HDA-RRMS from the payer perspective in the KSA.

Identifiants

pubmed: 34425468
pii: S2212-1099(21)00079-0
doi: 10.1016/j.vhri.2021.03.007
pii:
doi:

Substances chimiques

Immunosuppressive Agents 0
Tablets 0
Cladribine 47M74X9YT5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

189-195

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Saeed Bohlega (S)

King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Ahmed Elboghdady (A)

Merck Serono Middle East FZ LTD, an affiliate of Merck KGaA, Darmstadt, Germany.

Awatef Al-Johani (A)

Ministry of Health, Riyadh, Saudi Arabia.

Koshu Mahajan (K)

IQVIA, Gurgaon, India.

Majdoline Khalil Mughari (MK)

Ministry of Health, Makkah, Saudi Arabia.

Mai Al-Saqa'aby (M)

King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Omneya Mohamed (O)

IQVIA, Dubai, United Arab Emirates. Electronic address: omneya.mohamed@iqvia.com.

Rola Alarieh (R)

King Fahad Medical City, Riyadh, Saudi Arabia.

Yaser Al Malik (Y)

King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, Saudi Arabia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH