Extended-interval dosing of natalizumab in NOVA
- PMID: 36804084
- DOI: 10.1016/S1474-4422(23)00032-7
Extended-interval dosing of natalizumab in NOVA
Conflict of interest statement
OS is funded by a Merit Review grant (federal award document number BX005664-01) from the US Department of Veterans Affairs, Biomedical Laboratory Research and Development; is funded by RFA-2203-39314 (principal investigator) and RFA-2203-39305 (co-principal investigator) grants from the National Multiple Sclerosis Society; is a 2021 recipient of a Grant for Multiple Sclerosis Innovation, Merck; serves on the editorial board of Therapeutic Advances in Neurological Disorders; has served on data monitoring committees for Genentech/Roche, Novartis, Pfizer, and TG Therapeutics without monetary compensation; has served on a clinical trial steering committee for EMD Serono without monetary compensation; has advised EMD Serono, Genentech, Genzyme, TG Therapeutics, and VYNE Therapeutics; and received grant support from EMD Serono and Exalys. BT declares no competing interests.
Comment in
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Extended-interval dosing of natalizumab in NOVA - Authors' reply.Lancet Neurol. 2023 Mar;22(3):200-201. doi: 10.1016/S1474-4422(23)00034-0. Lancet Neurol. 2023. PMID: 36804085 No abstract available.
Comment on
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Comparison of switching to 6-week dosing of natalizumab versus continuing with 4-week dosing in patients with relapsing-remitting multiple sclerosis (NOVA): a randomised, controlled, open-label, phase 3b trial.Lancet Neurol. 2022 Jul;21(7):608-619. doi: 10.1016/S1474-4422(22)00143-0. Epub 2022 Apr 25. Lancet Neurol. 2022. PMID: 35483387 Clinical Trial.
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