ALS patients continue experimental oral treatment in safety Follow-Up

NCT ID NCT05568615

Summary

This study followed patients who completed earlier trials of oral edaravone for ALS to monitor long-term safety. Fifteen participants in Japan took the medication in cycles until it became commercially available or until August 2023. The main goal was to track side effects and adverse reactions to understand the treatment's safety profile over extended use.

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Contacts and locations

Locations

  • Fukushima Medical University Hospital

    Fukushima, Fukushima, 960-1295, Japan

  • Kagawa University Hospital

    Kita-gun, Kagawa-ken, 761-0793, Japan

  • Kitasato University Hospital

    Sagamihara-shi, Kanagawa, 252-0375, Japan

  • National Epilepsy Center NHO Shizuoka Institute of Epilepsy and Neurological Disorders

    Shizuoka, 420-8688, Japan

  • National Hospital Organization Chibahigashi National Hospital

    Chiba, Chiba, 260-8712, Japan

  • National Hospital Organization Higashinagoya National Hospital

    Nagoya, Aichi-ken, 465-8620, Japan

  • National Hospital Organization Kumamoto Saishun Medical Center

    Kōshi, Kumamoto, 861-1196, Japan

  • National Hospital Organization Osaka Toneyama Medical Center

    Toyonaka-shi, Osaka, 560-8552, Japan

  • Shiga University of Medical Science Hospital

    Ōtsu, Shiga, 520-2192, Japan

  • Tokyo Metropolitan Neurological Hospital

    Fuchu-shi, Tokyo, 183-0042, Japan

  • Yokohama City University Hospital

    Yokohama, Kanagawa, 236-0004, Japan

Conditions

Explore the condition pages connected to this study.