Literature DB >> 28872911

What can we learn from the edaravone development program for ALS?

Nicholas J Maragakis1.   

Abstract

Edaravone's development into an ALS therapeutic has been a process which began with preclinical studies regarding its potential in targeting ALS. Despite edaravone's inability to show benefit in a general ALS population, an important post-hoc analysis showed that a clinical subset of patients had benefit. Most importantly, a subsequent study examining the capacity of edaravone to have benefit in this specific subset of ALS patients was successful in meeting its primary outcome measures. Questions regarding whether the dosing regimen could be simplified or improved, the duration of the effects, and the timing of the potential treatment to different stages of disease remain to be answered. However, the benefit of this compound in delivering a meaningful therapy to ALS patients and the lessons learned with regard to its development should widen interest in clinical research so that additional strategies for treating ALS may become available to patients.

Entities:  

Keywords:  Therapy; clinical trial; drug; motor neuron disease

Mesh:

Substances:

Year:  2017        PMID: 28872911     DOI: 10.1080/21678421.2017.1361446

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Frontotemporal Degener        ISSN: 2167-8421            Impact factor:   4.092


  6 in total

Review 1.  Hereditary Motor Neuropathies and Amyotrophic Lateral Sclerosis: a Molecular and Clinical Update.

Authors:  Rocio Garcia-Santibanez; Matthew Burford; Robert C Bucelli
Journal:  Curr Neurol Neurosci Rep       Date:  2018-10-17       Impact factor: 5.081

2.  Edaravone efficacy in amyotrophic lateral sclerosis with reduced forced vital capacity: Post-hoc analysis of Study 19 (MCI186-19) [clinical trial NCT01492686].

Authors:  Benjamin Rix Brooks; Terry Heiman-Patterson; Martina Wiedau-Pazos; Shawn Liu; Jeffrey Zhang; Stephen Apple
Journal:  PLoS One       Date:  2022-06-14       Impact factor: 3.752

3.  MicroRNA-5572 Is a Novel MicroRNA-Regulating SLC30A3 in Sporadic Amyotrophic Lateral Sclerosis.

Authors:  Hisaka Kurita; Saori Yabe; Tomoyuki Ueda; Masatoshi Inden; Akiyoshi Kakita; Isao Hozumi
Journal:  Int J Mol Sci       Date:  2020-06-24       Impact factor: 5.923

4.  ALS blood expression profiling identifies new biomarkers, patient subgroups, and evidence for neutrophilia and hypoxia.

Authors:  William R Swindell; Colin P S Kruse; Edward O List; Darlene E Berryman; John J Kopchick
Journal:  J Transl Med       Date:  2019-05-22       Impact factor: 5.531

5.  Assessment of Therapeutic Response of Edaravone and Riluzole Combination Therapy in Amyotrophic Lateral Sclerosis Patients.

Authors:  Swapnil Samadhiya; Vijay Sardana; Bharat Bhushan; Dilip Maheshwari; Ravi Goyal
Journal:  Ann Indian Acad Neurol       Date:  2022-06-09       Impact factor: 1.714

6.  Inhibition of Drp1/Fis1 interaction slows progression of amyotrophic lateral sclerosis.

Authors:  Amit U Joshi; Nay L Saw; Hannes Vogel; Anna D Cunnigham; Mehrdad Shamloo; Daria Mochly-Rosen
Journal:  EMBO Mol Med       Date:  2018-03       Impact factor: 12.137

  6 in total

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