Ravulizumab (Ultomiris)

None CADTH
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 CADTH reimbursement reviews are comprehensive assessments of the clinical effectiveness and cost-effectiveness, as well as patient and clinician perspectives, of a drug or drug class.
 The assessments inform non-binding recommendations that help guide the reimbursement decisions of Canada's federal, provincial, and territorial governments, with the exception of Quebec.
 This review assesses ravulizumab (Ultomiris) for injection, 10 mg/mL and 100 mg/mL concentrate for solution for IV infusion.
 Indication: For the treatment of adult patients with anti-acetylcholine receptor antibody–positive generalized myasthenia gravis.
","PeriodicalId":9437,"journal":{"name":"Canadian Journal of Health Technologies","volume":"5 6","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian Journal of Health Technologies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51731/cjht.2023.770","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

CADTH reimbursement reviews are comprehensive assessments of the clinical effectiveness and cost-effectiveness, as well as patient and clinician perspectives, of a drug or drug class. The assessments inform non-binding recommendations that help guide the reimbursement decisions of Canada's federal, provincial, and territorial governments, with the exception of Quebec. This review assesses ravulizumab (Ultomiris) for injection, 10 mg/mL and 100 mg/mL concentrate for solution for IV infusion. Indication: For the treatment of adult patients with anti-acetylcholine receptor antibody–positive generalized myasthenia gravis.
拉武利珠单抗(Ultomiris)
& # x0D;CADTH报销审查是对药物或药物类别的临床有效性和成本效益以及患者和临床医生观点的综合评估。 评估结果提供了非约束性建议,这些建议有助于指导加拿大联邦、省和地区政府(魁北克省除外)的报销决定。本综述评估了注射用拉乌利珠单抗(Ultomiris)、10 mg/mL和100 mg/mL静脉滴注浓缩液。适应症:用于抗乙酰胆碱受体抗体阳性的成人全身性重症肌无力患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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