Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164895
Title: Masitinib as an add-on therapy to riluzole in patients with amyotrophic lateral sclerosis: a randomized clinical trial
Author: Mora, Jesús S.
Genge, Angela
Chio, Adriano
Estol, Conrado J.
Chaverri, Delia
Hernández, María
Marín, Saúl
Mascias, Javier
Rodríguez, Gabriel E.
Povedano, Mònica
Paipa, Andres
Domínguez, Raul
Gamez, Josep
Salvado, Maria
Lunetta, Christian
Ballario, Carlos
Riva, Nilo
Mandrioli, Jessica
Moussy, Alain
Kinet, Jean-Pierre
Auclair, Christian
Dubreuil, Patrice
Arnold, Vincent
Mansfield, Colin D.
Hermine, Olivier
The Ab10015 Study Group
Keywords: Assaigs clínics
Terapèutica
Proteïnes quinases
Clinical trials
Therapeutics
Protein kinases
Issue Date: 7-Jul-2019
Publisher: Informa UK Limited
Abstract: Objective: To assess masitinib in the treatment of ALS. Methods: Double-blind study, randomly assigning 394 patients (1:1:1) to receive riluzole (100 mg/d) plus placebo or masitinib at 4.5 or 3.0 mg/kg/d. Following a blinded transition from phase 2 to phase 2/3, a prospectively defined two-tiered design was implemented based on ALSFRS-R progression rate from disease-onset to baseline (ΔFS). This approach selects a more homogeneous primary efficacy population (“Normal Progressors”, ΔFS < 1.1 points/month) while concurrently permitting secondary assessment of the broader population. Primary endpoint was decline in ALSFRS-R at week-48 (ΔALSFRS-R), with the high-dose “Normal Progressor” cohort being the prospectively declared primary efficacy population. Missing data were imputed via last observation carried forward (LOCF) methodology with sensitivity analyses performed to test robustness. Results: For the primary efficacy population, masitinib (n = 99) showed significant benefit over placebo (n = 102) with a ΔALSFRS-R between-group difference (ΔLSM) of 3.4 (95% CI 0.65–6.13; p = 0.016), corresponding to a 27% slowing in rate of functional decline (LOCF methodology). Sensitivity analyses were all convergent, including the conservative multiple imputation technique of FCS-REGPMM with a ΔLSM of 3.4 (95% CI 0.53–6.33; p = 0.020). Secondary endpoints (ALSAQ-40, FVC, and time-to-event analysis) were also significant. Conversely, no significant treatment-effect according to ΔALSFRS-R was seen for the broader “Normal and Fast Progressor” masitinib 4.5 mg/kg/d cohort, or either of the low-dose (masitinib 3.0 mg/kg/d) cohorts. Rates of treatment-emergent adverse events (AEs) (regardless of causality or post-onset ΔFS) were 88% with masitinib 4.5 mg/kg/d, 85% with 3.0 mg/kg/d, and 79% with placebo. Likewise, rates of serious AE were 31, 23, and 18%, respectively. No distinct event contributed to the higher rate observed for masitinib and no deaths were related to masitinib. Conclusions: Results show that masitinib at 4.5 mg/kg/d can benefit patients with ALS. A confirmatory phase 3 study will be initiated to substantiate these data.
Note: Reproducció del document publicat a: https://doi.org/10.1080/21678421.2019.1632346
It is part of: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2020, vol. 21, issue. 1, p. 5-14
URI: http://hdl.handle.net/2445/164895
Related resource: https://doi.org/10.1080/21678421.2019.1632346
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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