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Pharmacoeconomic review report : Dupilumab (Dupixent) (Sanofi-Aventis Canada Inc.) / Canadian Agency for Drugs and Technologies in Health.
- Format:
- Book
- Author/Creator:
- Canadian Agency for Drugs and Technologies in Health, author, issuing body.
- Series:
- Common drug review clinical review report.
- Common drug review clinical review report
- Language:
- English
- Subjects (All):
- Drugs--Cost effectiveness.
- Drugs.
- Physical Description:
- 1 online resource.
- Edition:
- Final edition.
- Place of Publication:
- Ottawa, ON : CADTH, 2018.
- Summary:
- Dupilumab (Dupixent) is indicated for use in adult patients with moderate-to-severe atopic dermatitis whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable. Dupilumab can be used with or without topical corticosteroids (TCS). The dosage form is 150 mg/mL solution in a pre-filled syringe, intended for patients to self-administer subcutaneously. The recommended dosage for adult patients is an initial dose of 600 mg (two 300 mg injections), followed by 300 mg injected every other week. At the submitted price of 1,153.85 dollars per 300 mg dose, the first-year cost of dupilumab is 31,154 dollars, and 30,000 dollars annually thereafter. The manufacturer submitted a cost-utility analysis (CUA) of dupilumab as an add-on to current standard of care (SOC) in patients with moderate-to-severe atopic dermatitis whose disease is not adequately controlled with topical prescription therapies.
- Contents:
- Abbreviations
- Executive Summary
- Background
- Summary of Identified Limitations and Key Results
- Conclusions
- Information on the Pharmacoeconomic Submission
- Summary of the Manufacturer's Pharmacoeconomic Submission
- Manufacturer's Base Case
- Summary of Manufacturer's Sensitivity Analyses
- Limitations of Manufacturer's Submission
- CADTH Common Drug Review Reanalyses
- Issues for Consideration
- Patient Input
- Appendix 1. Cost Comparison
- Appendix 2. Summary of Key Outcomes
- Appendix 3. Additional Information
- Appendix 4. Summary of Other Health Technology Assessment Reviews of Drug
- Appendix 5. Reviewer Worksheets
- References.
- Notes:
- Description based on publisher supplied metadata and other sources.
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