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Cover of Pharmacoeconomic Report: Satralizumab (Enspryng)

Pharmacoeconomic Report: Satralizumab (Enspryng)

(Hoffmann-La Roche Limited)

Indication: Neuromyelitis optica spectrum disorder

CADTH Common Drug Review

CADTH undertook reanalyses of the sponsor’s economic models for satralizumab administered as monotherapy and in combination with immunosuppressive therapies (IST) to address some of the identified limitations. In both models, CADTH’s base-case reanalysis included a definition of relapse that is more reflective of clinical practice and removed caregiver disutilities. In addition, in the economic model for satralizumab plus IST compared with IST alone, CADTH further assumed no differences in the frequency of adverse events between groups. CADTH’s findings remained aligned with the sponsor, such that satralizumab is not cost-effective at a $50,000 per quality-adjusted life-year (QALY) willingness-to-pay (WTP) threshold as monotherapy or in combination with IST. The incremental cost-effectiveness ratio (ICER) for satralizumab monotherapy versus no treatment was $337,535 per QALY gained, and the ICER for satralizumab plus IST versus IST alone was $752,179 per QALY gained. Price-reduction analyses suggest that, for satralizumab to achieve an ICER below $50,000 per QALY gained, reductions in the price by 80% when administered as monotherapy, and 89% when administered in combination with IST, would be required.

Relapse was incorporated into the model as the main treatment-effectiveness measure to define progression and movement within the sponsor’s economic model. As such, the model results were primarily driven by the definition of relapse. The incremental benefit ofsatralizumab as monotherapy or as an add-on therapy to IST was minimal over the trial’s observed period, while the majority (approximately 98%) of the incremental benefits were achieved over the remainder of the extrapolated time horizon under the assumption of persistent treatment effects over time. CADTH was further unable to address the inherent limitations with the conceptualization of the economic model and the uncertainties resulting from the overestimation of life-years.

Given the lack of comparative clinical information, the cost-effectiveness of satralizumab compared with IST, and compared with eculizumab, is unknown.

Version: Final (with redactions)

Funding: CADTH receives funding from Canada’s federal, provincial, and territorial governments, with the exception of Quebec.

Disclaimer: The information in this document is intended to help Canadian health care decision-makers, health care professionals, health systems leaders, and policy-makers make well-informed decisions and thereby improve the quality of health care services. While patients and others may access this document, the document is made available for informational purposes only and no representations or warranties are made with respect to its fitness for any particular purpose. The information in this document should not be used as a substitute for professional medical advice or as a substitute for the application of clinical judgment in respect of the care of a particular patient or other professional judgment in any decision-making process. The Canadian Agency for Drugs and Technologies in Health (CADTH) does not endorse any information, drugs, therapies, treatments, products, processes, or services.

While care has been taken to ensure that the information prepared by CADTH in this document is accurate, complete, and up-to-date as at the applicable date the material was first published by CADTH, CADTH does not make any guarantees to that effect. CADTH does not guarantee and is not responsible for the quality, currency, propriety, accuracy, or reasonableness of any statements, information, or conclusions contained in any third-party materials used in preparing this document. The views and opinions of third parties published in this document do not necessarily state or reflect those of CADTH.

CADTH is not responsible for any errors, omissions, injury, loss, or damage arising from or relating to the use (or misuse) of any information, statements, or conclusions contained in or implied by the contents of this document or any of the source materials.

This document may contain links to third-party websites. CADTH does not have control over the content of such sites. Use of third-party sites is governed by the third-party website owners’ own terms and conditions set out for such sites. CADTH does not make any guarantee with respect to any information contained on such third-party sites and CADTH is not responsible for any injury, loss, or damage suffered as a result of using such third-party sites. CADTH has no responsibility for the collection, use, and disclosure of personal information by third-party sites.

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About CADTH: CADTH is an independent, not-for-profit organization responsible for providing Canada’s health care decision-makers with objective evidence to help make informed decisions about the optimal use of drugs, medical devices, diagnostics, and procedures in our health care system.

Copyright © 2021 Canadian Agency for Drugs and Technologies in Health.

The copyright and other intellectual property rights in this document are owned by CADTH and its licensors. These rights are protected by the Canadian Copyright Act and other national and international laws and agreements. Users are permitted to make copies of this document for non-commercial purposes only, provided it is not modified when reproduced and appropriate credit is given to CADTH and its licensors.

Except where otherwise noted, this work is distributed under the terms of a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International licence (CC BY-NC-ND), a copy of which is available at http://creativecommons.org/licenses/by-nc-nd/4.0/

Bookshelf ID: NBK583281PMID: 36063475

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