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*Posters presented at conferences do not undergo peer review and should not be considered a replacement for a complete article published in a peer-reviewed journal.

Edaravone mitigates TDP-43 mislocalization in human amyotrophic lateral sclerosis neurons with potential implication of the SIRT1-XBP1 pathway
Mikuriya S, Takegawa-Araki T, Tamura M. Free Radical Biology and Medicine. 2025; 230: 283-293. https://doi.org/10.1016/j.freeradbiomed.2025.01.012
Safety Extension Study of Edaravone Oral Suspension in Patients With Amyotrophic Lateral Sclerosis for up to an Additional 96 Weeks of Treatment
Genge A, Pattee GL, et al. Safety Extension Study of Edaravone Oral Suspension in Patients With Amyotrophic Lateral Sclerosis for up to an Additional 96 Weeks of Treatment. Muscle Nerve. 2025 Sep;72(3):450-454. https://onlinelibrary.wiley.com/doi/10.1002/mus.28451
Treatment Patterns and Survival Benefit of Edaravone-Treated People With Amyotrophic Lateral Sclerosis in the ALS/MND Natural History Consortium
Sherman AV, Zhang J, Liu Y, et al. Poster* presented at The European Network to Cure ALS (ENCALS) Annual Meeting; June 17-20, 2024.
Intravenous edaravone treatment in ALS and survival: an exploratory, retrospective, administrative claims analysis
Brooks BR, Berry JD, Ciepielewska M, et al. eClinicalMedicine. 2022;52:101590.
doi:10.1016/j.eclinm.2022.101590
Edaravone administered orally and via nasogastric tube in healthy adults: a comparative bioavailability phase 1 study
Shimizu H, Nishimura Y, Shiide Y. Clin Pharmacol Drug Dev. Published online Oct 12, 2022. doi:10.1002/cpdd.1175
Long-term edaravone efficacy in amyotrophic lateral sclerosis: post-hoc analyses of Study 19 (MCI186-19)
Shefner J, Heiman-Patterson T, Pioro EP, et al. Muscle Nerve. 2020;61(2):218-221.
doi:10.1002/mus.26740
Analysis of the US safety data for edaravone (Radicava®) from the third year after launch
Genge A, Brooks BR, Oskarsson B, et al. Drugs R D. 2022;22(3):205-211. doi:10.1007/s40268-022-00391-6
Edaravone efficacy in amyotrophic lateral sclerosis with reduced forced vital capacity: post-hoc analysis of Study 19 (MCI186-19)
[clinical trial NCT01492686]
Brooks BR, Heiman-Patterson T, Wiedau-Pazos M, et al. PloS One. 2022;17(6):e0258614.
doi:10.1371/journal.pone.0258614
Engaging ALS patients and caregivers (the ALS research ambassadors) to help design the REFINE-ALS biomarker study
Berry JD, Bedlack R, Mathews D, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2021;22(1-2):147-150. doi:10.1080/21678421.2020.1804939
Evidence for generalizability of edaravone efficacy using a novel machine learning risk-based subgroup analysis tool
Brooks BR, Pioro EP, Beaulieu D, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2022;23(1-2):49-57. doi:10.1080/21678421.2021.1927102
Clinical staging in amyotrophic lateral sclerosis: analysis of edaravone Study 19
Al-Chalabi A, Chiò A, Merrill C, et al. J Neurol Neurosurg Psychiatry. 2021;92(2):165-171.
doi:10.1136/jnnp-2020-323271
Treatment persistence among amyotrophic lateral sclerosis patients receiving intravenous edaravone: results from a national infusion center
Hagan M, Ciepielewska M, Harrison A, et al. Poster presented at virtual 31st International Symposium on ALS/MND; December 9-11, 2020.
Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial
The Writing Group on behalf of the Edaravone (MCI-186) ALS 19 Study Group. Lancet Neurol. 2017;16(7):505-512. doi:10.1016/S1474-4422(17)30115-1
Post-hoc analyses of the edaravone clinical trials Study 16 and Study 19: a step toward more efficient clinical trial designs in amyotrophic lateral sclerosis
Palumbo JM, Hubble J, Apple S, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2019;20(5-6):421-431. doi:10.1080/21678421.2019.1599955
A post-hoc subgroup analysis of outcomes in the first phase III clinical study of edaravone (MCI-186) in amyotrophic lateral sclerosis
The Edaravone (MCI-186) ALS 16 Study Group. Amyotroph Lateral Scler Frontotemporal Degener. 2017;18(Sup1):11-19. doi:10.1080/21678421.2017.1363780
Bioequivalence Study of Oral Suspension and Intravenous Formulation of Edaravone in Healthy Adult Subjects
Shimizu H, Nishimura Y, Shiide Y, et al. Clin. Pharmacol. Drug Dev. 2021; 10: 1188-1197. doi: 10.1002/cpdd.952
Evaluation of Pharmacokinetics, Safety, and Drug-Drug Interactions of an Oral Suspension of Edaravone in Healthy Adults
Shimizu H, Nishimura Y, Shiide Y, et al. Clin. Pharmacol. Drug Dev. 2021; 10: 1174-1187. doi: 10.1002/cpdd.925
Food Effect Study to Assess the Impact on Edaravone Pharmacokinetic Profiles in Healthy Participants
Hidetoshi H, Nishimura Y, Shiide Y, et al. Clin. Ther., Volume 44, Issue 12, 2022, Pages 1552-1565, ISSN 0149-2918. doi: 10.1016/j.clinthera.2022.10.001.
Confirmatory double-blind, parallel-group, placebo-controlled study of efficacy and safety of edaravone (MCI-186) in amyotrophic lateral sclerosis patients
Abe K, Itoyama Y, Sobue G, et al. 2014. Amyotroph Lateral Scler Frontotemporal Degener, 15(7-8):610-617. doi: 10.3109/21678421.2014.959024
Edaravone Administered Orally and Via Nasogastric Tube in Healthy Adults: A Comparative Bioavailability Phase 1 Study
Shimizu H, Nishimura Y, Shiide Y, et al. Clin. Pharmacol. Drug Dev. 2023. 12: 77-84. Doi: 10.1002/cpdd.1175