"Faricimab"

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                            Faricimab for treating visual impairment caused by macular oedema after retinal vein occlusion Faricimab for treating visual impairment caused by macular oedema after retinal vein occlusion Technology appraisal guidance Published: 11 September 2024 www.nice.org.uk/guidance/ta1004 © NICE 2024. All rights reserved. Subject to Notice of rights ( responsibility The recommendations in this guidance and to reduce health inequalities. Commissioners and providers have a responsibility to promote an environmentally sustainable health and care system and should assess and reduce the environmental impact of implementing NICE recommendations wherever possible. Faricimab for treating visual impairment caused by macular oedema after retinal veinocclusion (TA1004)© NICE 2024. All rights reserved. Subject
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                            2025Institute for Quality and Efficiency in Healthcare (IQWiG)
                            Review Analysis
                            Appears Promising
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                            Faricimab (visual impairment due to macular oedema secondary to retinal vein occlusion) ' Benefit assessment according to '35a Social Code Book V 1 Translation of Sections I 1 to I 6 of the dossier assessment Faricimab (Visusbeeinträchtigung infolge eines Makulaödems bei retinalem Venenverschlusses) – Nutzenbewertung gemäß § 35a SGB V. Please note: This translation is provided as a service by IQWiG to English-language readers. However, solely the German original text is absolutely authoritative and legally binding. Faricimab (visual impairment due to macular oedema secondary to retinal vein occlusion) Benefit assessment according to §35a SGB V1 EXTRACT Project: A24-85 Version: 1.0 Status: 20 Nov 2024 DOI: 10.60584/A24-85_en Extract of dossier assessment A24-85 Version 1.0 Faricimab
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                            Faricimab (Vabysmo) Terms of use - Canada.ca * Skip to main content * Skip to "About government" Language selection * Français SearchSearch Canada.ca Search Topics menuMain Menu You are here: 1. Home 2. Health 3. Drug and health products 4. Licensing, authorizing and manufacturing drug and health products 5. Drug and health product review and approval 6. Clinical information on drugs and health
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                            2024Prescrire
                            Faricimab (Vabysmo) in age-related macular degeneration or diabetic macular oedema Prescrire IN ENGLISH - Spotlight ''Faricimab (Vabysmo°) in age-related macular degeneration or diabetic macular oedema'', 1 June 2024 {1}##LOC[OK]## {1} ##LOC[OK]## ##LOC[Cancel]## {1}##LOC[OK]####LOC[Cancel]## Register online| Log in| My Prescrire Issue contents * Current issue * Last 12 issues * All issues Topics subscription * Solidarity Subscription Rate * Subscribers: register online * Prescrire's other products * Free Special Edition * Sign up to receive the newsletter english.prescrire.org > Spotlight > 100 most recent > Faricimab (Vabysmo°) in age-related macular degeneration or diabetic macular oedema SpotlightEvery month, the subjects in Prescrire’s Spotlight. 100 most recent: 1|10|20|30|40|50|60|70|80|90
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                            2023Institute for Quality and Efficiency in Healthcare (IQWiG)
                            Review Analysis
                            Appears Promising
                            ?
                            Faricimab (visual impairment due to diabetic macular oedema) ' Benefit assessment acc. to ' 35a Social Code Book V 1 Translation of Sections I 1 to I 6 of the dossier assessment Faricimab (Visusbeeinträchtigung infolge eines diabetischen Makulaödems) – Nutzenbewertung gemäß § 35a SGB V. Please note: This document was translated by an external translator and is provided as a service by IQWiG to English-language readers. However, solely the German original text is absolutely authoritative and legally binding. Faricimab (visual impairment due to diabetic macular oedema) – Benefit assessment according to §35a SGB V1 EXTRACT Project: A22-109 Version: 1.0 Status: 12 January 2023 Extract of dossier assessment A22-109 Version 1.0 Faricimab ( visual impairment due to diabetic macular oedema 12
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                            2023Institute for Quality and Efficiency in Healthcare (IQWiG)
                            Review Analysis
                            Appears Promising
                            ?
                            Faricimab (neovascular age-related macular degeneration) ' Benefit assessment according to ' 35a Social Code Book V 1 Translation of Sections I 1 to I 6 of the dossier assessment Faricimab (neovaskuläre altersabhängige Makuladegeneration) – Nutzenbewertung gemäß § 35a SGB V. Please note: This translation is provided as a service by IQWiG to English-language readers. However, solely the German original text is absolutely authoritative and legally binding. Faricimab (neovascular age-related macular degeneration) Benefit assessment according to §35a SGB V1 EXTRACT Project: A22-110 Version: 1.0 Status: 11 January 2023 Extract of dossier assessment A22-110 Version 1.0 Faricimab ( neovascular age-related macular degeneration) 11 January 2023 Institute for Quality and Efficiency in Health Care
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                            Faricimab for treating diabetic macular oedema Faricimab for treating diabetic macular oedema Technology appraisal guidance Published: 29 June 2022 www.nice.org.uk/guidance/ta799 © NICE 2022. All rights reserved. Subject to Notice of rights (https://www.nice.org.uk/terms-and-conditions#notice-of-rights).Your responsibility Your responsibility The recommendations in this guidance represent recommendations wherever possible. Faricimab for treating diabetic macular oedema (TA799)© NICE 2022. All rights reserved. Subject to Notice of rights (https://www.nice.org.uk/terms-and-conditions#notice-of-rights).Page 2 of11Contents Contents 1 Recommendations ......................................................................................................................................................4
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                            Faricimab for treating wet age-related macular degeneration Faricimab for treating wet age-related macular degeneration Technology appraisal guidance Published: 29 June 2022 www.nice.org.uk/guidance/ta800 © NICE 2022. All rights reserved. Subject to Notice of rights (https://www.nice.org.uk/terms-and-conditions#notice-of-rights).Your responsibility Your responsibility The recommendations impact of implementing NICE recommendations wherever possible. Faricimab for treating wet age-related macular degeneration (TA800)© NICE 2022. All rights reserved. Subject to Notice of rights (https://www.nice.org.uk/terms-and-conditions#notice-of-rights).Page 2 of12Contents Contents 1 Recommendations
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                            2024Scottish Medicines Consortium
                            Faricimab (Vabysmo) - treatment of adult patients with visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO) Published 07 October 2024 Advice document SMC2685 faricimab solution for injection (Vabysmo®) Roche 06 September 2024 The Scottish Medicines Consortium (SMC) has completed its assessment of the above product and, following review by the SMC executive, advises NHS Boards and Area Drug and Therapeutics Committees (ADTCs) on its use in NHSScotland. The advice is summarised as follows: ADVICE: following an abbreviated submission faricimab (Vabysmo®) is accepted for use within NHSScotland. Indication under review: treatment of adult patients with visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO
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                            Faricimab (Vabysmo) Skip to main contentSwitch to basic HTML versionLanguage selectionFrançaisSearchSearch Canada.caSearchTopics menuMAINMENU You are here:Home Health Drug and health products Licensing, authorizing and manufacturing drug and health products Drug and health product review and approval Clinical information on drugs and health products Search for clinical information on drugs
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                            2022European Medicines Agency - EPARs
                            Faricimab (Vabysmo) - age-related macular degeneration (AMD) Official address Domenico Scarlattilaan 6 ● 1083 HS Amsterdam ● The Netherlands An agency of the European Union Address for visits and deliveries Refer to www.ema.europa.eu/how-to-find-us Send us a question Go to www.ema.europa.eu/contact Telephone +31 (0)88 781 6000 © European Medicines Agency, 2022. Reproduction is authorised provided the source is acknowledged. EMA/666340/2022 EMEA/H/C/005642 Vabysmo (faricimab) An overview of Vabysmo and why it is authorised in the EU What is Vabysmo and what is it used for? Vabysmo is a medicine used to treat adults with: • the ‘wet’ form of age-related macular degeneration (AMD), a disease that affects the central part of the retina (called the macula) at the back of the eye
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                            Faricimab (Vabysmo) - neovascular (wet) age-related macular degeneration (AMD) and diabetic macular edema (DME) Skip to main contentSkip to "About this site"Government of CanadaSearch and menusSearch and menusYou are here:HomeAll ServicesHealthDrugs, health & consumer productsReview DecisionsSummary Basis of Decision - - Health CanadaDrugsNatural Health ProductsMedical DevicesReview Decisions
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                            2023CADTH - Reimbursement Review
                            Review Analysis
                            Appears Promising
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                            Faricimab (Vabysmo) - Diabetic macular edema Return to Article DetailsFaricimab (Vabysmo)
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                            2022CADTH - Reimbursement Review
                            Review Analysis
                            Appears Promising
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                            Faricimab (Vabysmo) - Macular degeneration, age-related Return to Article DetailsFaricimab (Vabysmo)
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                            2022CADTH - Reimbursement Review
                            Review Analysis
                            Appears Promising
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                            faricimab - Vabysmo - Macular degeneration, age-related Skip to main contentAboutCollaboration/OutreachPatient/CommunityCareersContactMy CADTHFRReportsResourcesProvide InputSubmit a RequestNews & EventsWhat Does The Evidence Say About...SearchBreadcrumbHome Reimbursement Reviews faricimabCopied to clipboard faricimab( Last Updated : November 16, 2022)Reimbursement ReviewAbout CADTH Reimbursement
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                            2022Scottish Medicines Consortium
                            Faricimab (Vabysmo) - neovascular (wet) age-related macular degeneration (nAMD) Published 12 December 2022 Product update SMC2512 faricimab 120mg/mL solution for injection (Vabysmo®) Roche Products Limited 04 November 2022 The Scottish Medicines Consortium (SMC) has completed its assessment of the above product and, following review by the SMC executive, advises NHS Boards and Area Drug and Therapeutics Committees (ADTCs) on its use in NHSScotland. The advice is summarised as follows: ADVICE: following an abbreviated submission faricimab (Vabysmo®) is accepted for use within NHSScotland. Indication under review: for the treatment of adult patients with neovascular (wet) age-related macular degeneration (nAMD). Faricimab offers an additional treatment choice in the therapeutic class
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                            2022Scottish Medicines Consortium
                            Faricimab (Vabysmo) - For the treatment of adult patients with visual impairment due to diabetic macular oedema (DMO) 1 Published 07 November 2022 1 SMC2499 faricimab 120mg/mL solution for injection (Vabysmo®) Roche Products Limited 07 October 2022 The Scottish Medicines Consortium (SMC) has completed its assessment of the above product and, following review by the SMC executive, advises NHS Boards and Area Drug and Therapeutics Committees (ADTCs) on its use in NHSScotland. The advice is summarised as follows: ADVICE: following a full submission faricimab (Vabysmo®) is accepted for restricted use within NHSScotland. Indication under review: For the treatment of adult
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                            Targeting the Tie-2 Receptor with Faricimab in Central Serous Chorioretinopathy: A Case Series Motivated by a Genetic Finding: Faricimab in central serous chorioretinopathy. To investigate the effects of faricimab, a bispecific antibody targeting VEGF and Ang-2 (thus increasing Tie-2 activity), in patients with CSC based on a recent genetic study that implicated Tie-2 signaling in CSC pathophysiology. A retrospective interventional multicenter case series. We included patients with chronic CSC (persistent or recurrent SRF for ≥6 months) who received at least one faricimab 6mg injection between January 1 2022 and April 1 2024. Study sites included Massachusetts Eye and Ear and University of California San Francisco. Patients with evidence of a choroidal neovascular membrane on color photos
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                            2024PLoS ONE
                            Optimization of individualized faricimab dosing for patients with diabetic macular edema: Protocol for the SWAN open-label, single-arm clinical trial.