HELPFUL RESOURCES
HELPFUL RESOURCES
See which program might be right for your patient
No matter what type of health insurance your patient has, they may have options to help them afford their medicine
Get answers to common questions about support and resources from Genentech for patients who have been prescribed VABYSMO
This brochure is designed to help your patients get the support they need to access VABYSMO
For more information on individual resources, please visit the Helpful Resources for Your Practice page.
†The Product and Administration Co-pay Programs (“Programs”) are valid ONLY for patients with commercial (private or non-governmental) insurance who have a valid prescription for a Food and Drug Administration (FDA)-approved indication of a Genentech medicine. The Programs are not available to patients whose prescriptions are reimbursed under any federal state, or government-funded insurance programs (included but not limited to Medicare, Medicare Advantage, Medigap, Medicaid, TRICARE, Department of Defense, or Veterans Affairs Programs) or where prohibited by law or by the patient's health insurance provider. If at any time a patient begins receiving prescription drug coverage under any such federal, state or government- funded healthcare programs, the patient will no longer be eligible for the Programs. Under the Programs, the patient may be required to pay a co-pay for drug costs and a co-pay for administration costs. The final amount owed by a patient may be as little as $0 for the Genentech medicine or administration of the Genentech medicine (see Program specific details available at the Program website). The total patient out-of-pocket cost is dependent on the patient’s health insurance plan. The Programs assist with the cost of the Genentech medicine and the administration of the Genentech medicine only. It does not assist with the cost of other administrations, medicines, procedures or office visit fees. After reaching the maximum Programs’ benefit amounts, the patient will be responsible for all remaining out-of- pocket expenses. The amount of the Programs’ benefits cannot exceed the patient’s out-of-pocket expenses for the cost of the Genentech medicine or administration fees for the Genentech medicine. All participants are responsible for reporting the receipt of all Programs’ benefits as required by any insurer or by law. The Programs are only valid in the United States and U.S. Territories and are void where prohibited by law. The Drug Co-pay Program shall follow state restrictions in relation to AB-rated generic equivalents (e.g., MA, CA) where applicable. The Administration Co-pay Program is not valid for patients who reside or receive treatment in a restricted state (e.g. Massachusetts or Rhode Island). No party may seek reimbursement for all or any part of the benefit received through the Programs. The value of the Programs is intended exclusively for the benefit of the patient. The funds made available through the Programs may only be used to reduce the out-of-pocket costs for the patient enrolled in the Programs. The Programs are not intended for the benefit of third parties, including without limitation third party payers, pharmacy benefit managers, or their agents. If Genentech determines that a third party has implemented programs that adjust patient cost-sharing obligations based on the availability of support under the Programs and/or excludes the assistance provided under the Programs from counting towards the patient’s deductible or out-of-pocket cost limitations, Genentech may impose a per fill cap on the cost-sharing assistance available under the Programs. Submission of true and accurate information is a requirement for eligibility and Genentech reserves the right to disqualify patients who do not comply with Genentech Program Terms and Conditions. Genentech reserves the right to rescind, revoke or amend the Programs without notice at any time. Additional terms and conditions apply. Please visit the co-pay Program website for the full list of Terms and Conditions.
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VABYSMO [package insert]. South San Francisco, CA: Genentech, Inc; 2024.
VABYSMO [package insert]. South San Francisco, CA: Genentech, Inc; 2024.
Data on file. South San Francisco, CA: Genentech, Inc.
Data on file. South San Francisco, CA: Genentech, Inc.
Baumal CR, et al. Presented at American Academy of Ophthalmology (AAO) 2022. Sep 30–Oct 03 2022.
Baumal CR, et al. Presented at American Academy of Ophthalmology (AAO) 2022. Sep 30–Oct 03 2022.
Tadayoni R, et al. Presented at Angiogenesis, Exudation, and Degeneration 2023. Feb 10–11 2023.
Tadayoni R, et al. Presented at Angiogenesis, Exudation, and Degeneration 2023. Feb 10–11 2023.
Regula JT, et al. EMBO Mol Med. 2016;8:1265–1288.
Regula JT, et al. EMBO Mol Med. 2016;8:1265–1288.
Saharinen P, et al. Nat Rev Drug Discov. 2017;16:635–661.
Saharinen P, et al. Nat Rev Drug Discov. 2017;16:635–661.
Warmke N, et al. J Diabetes Complications. 2016;30:1643–1650.
Warmke N, et al. J Diabetes Complications. 2016;30:1643–1650.
Fiedler U, et al. Trends Immunol. 2006;27(12):552–558.
Fiedler U, et al. Trends Immunol. 2006;27(12):552–558.
Avery RL, et al. Presented at American Association of Ophthalmology (AAO) 2022. Sept 30–Oct 03 2022.
Avery RL, et al. Presented at American Association of Ophthalmology (AAO) 2022. Sept 30–Oct 03 2022.
Heier J, et al. Lancet. 2022;399(10326):729–740.
Heier J, et al. Lancet. 2022;399(10326):729–740.
London NJS, et al. Presented at Hawaiian Eye and Retina Meeting 2025. Jan 18–24 2025.
London NJS, et al. Presented at Hawaiian Eye and Retina Meeting 2025. Jan 18–24 2025.
Wykoff C, et al. Lancet. 2022;399(10326):741–755.
Wykoff C, et al. Lancet. 2022;399(10326):741–755.
Tadayoni R, et al. Presented at Angiogenesis, Exudation, and Degeneration 2024. Feb 03 2024.
Tadayoni R, et al. Presented at Angiogenesis, Exudation, and Degeneration 2024. Feb 03 2024.
Heier JS, et al. Presented at American Academy of Ophthalmology Retina Subspecialty Day (AAO-SSD) 2021. Nov 12–13 2021.
Heier JS, et al. Presented at American Academy of Ophthalmology Retina Subspecialty Day (AAO-SSD) 2021. Nov 12–13 2021.
Goldberg R, et al. Presented at the Association for Research in Vision and Ophthalmology (ARVO) 2023. April 23–27 2023.
Goldberg R, et al. Presented at the Association for Research in Vision and Ophthalmology (ARVO) 2023. April 23–27 2023.
Guymer R, et al. Presented at Angiogenesis, Exudation, and Degeneration 2022. Feb 11–12 2022.
Guymer R, et al. Presented at Angiogenesis, Exudation, and Degeneration 2022. Feb 11–12 2022.
Baumal CR, et al. Presented at the Association for Research in Vision and Ophthalmology (ARVO) 2022. May 1–4 2022.
Baumal CR, et al. Presented at the Association for Research in Vision and Ophthalmology (ARVO) 2022. May 1–4 2022.
Khanani AM, et al. JAMA Ophthalmol. 2020;138(9):964–972.
Khanani AM, et al. JAMA Ophthalmol. 2020;138(9):964–972.
Sahni J, et al. Ophthalmology. 2019;126(8):1155–1170.
Sahni J, et al. Ophthalmology. 2019;126(8):1155–1170.
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