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Mepolizumab (Nucala) [Internet]. Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2016 Nov.
Drug | mepolizumab (Nucala) |
---|---|
Indication | For the add-on maintenance treatment of adult patients with severe eosinophilic asthma who:
|
Reimbursement request | For the treatment of adult patients (≥ 18 years) with severe eosinophilic asthma (≥ 150 cells/mcL at treatment initiation or ≥ 300 cells/mcL in past 12 months) whose symptoms are inadequately controlled with high-dose inhaled corticosteroids and an additional asthma controller(s), and who have either experienced ≥ 2 exacerbations in the past 12 months or have dependency on systemic corticosteroids. |
Dosage form(s) | Lyophilized powder for subcutaneous injection, 100 mg/mL |
NOC date | 3 December 2015 |
Manufacturer | GlaxoSmithKline Inc. |
Contents
- ABBREVIATIONS
- EXECUTIVE SUMMARY
- 1. SUMMARY OF THE MANUFACTURER’S PHARMACOECONOMIC SUBMISSION
- 2. MANUFACTURER’S BASE CASE
- 3. SUMMARY OF MANUFACTURER’S SENSITIVITY ANALYSES
- 4. LIMITATIONS OF MANUFACTURER’S SUBMISSION
- 5. CADTH COMMON DRUG REVIEW REANALYSES
- 6. ISSUES FOR CONSIDERATION
- 7. PATIENT INPUT
- 8. CONCLUSIONS
- 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
- Pharmacoeconomic Review Report - Mepolizumab (Nucala)Pharmacoeconomic Review Report - Mepolizumab (Nucala)
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