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Taking people in JapanPhase 3

MSA-01 in Multiple System Atrophy

Key facts

Where
Bunkyo-ku, Bunkyō-Ku, Chiba, Fukuoka, Hasuda, Kagoshima, Kodaira, Kyoto, Nagoya, Okayama, Sapporo, and Yonago, JapanSee the 12 sites
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 30 and 79 years old?

Source: NCT07446894, who can take part

Where in Japan

  • Institute of Science Tokyo HospitalBunkyo-ku, JapanContact: Kinya IshikawaNot yet recruiting
  • The University of Tokyo HospitalBunkyō-Ku, JapanContact: Jun MitsuiTaking people
  • Chiba University HospitalChiba, JapanContact: Atsuhiko SugiyamaNot yet recruiting
  • Kyushu University HospitalFukuoka, JapanContact: Dai MatsuseNot yet recruiting
  • NHO Higashisaitama National HospitalHasuda, JapanContact: Katsuhisa OgataNot yet recruiting
  • Kagoshima University HospitalKagoshima, JapanContact: Yujiro HiguchiNot yet recruiting
  • National Center Hospital, National Center of Neurology and PsychiatryKodaira, JapanContact: Yuji TakahashiNot yet recruiting
  • Kyoto University HospitalKyoto, JapanContact: Hodaka YamakadoNot yet recruiting
  • Nagoya University HospitalNagoya, JapanContact: Masahisa KatsunoNot yet recruiting
  • Okayama University HospitalOkayama, JapanContact: Hiroyuki IshiuraNot yet recruiting
  • Hokkaido University HospitalSapporo, JapanContact: Ichiro YabeNot yet recruiting
  • Tottori University HospitalYonago, JapanContact: Ritsuko HanajimaNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Tokyo University
Trial code
NCT07446894
Record updated
4 March 2026
Original description
The purpose of this study is to evaluate whether MSA-01 slows the progression of multiple system atrophy (MSA) and to assess its safety.Read full original descriptionShow less

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase III Study of MSA-01 in Patients With Multiple System Atrophy

The purpose of this study is to evaluate whether MSA-01 slows the progression of multiple system atrophy (MSA) and to assess its safety.

The primary question is:

• Does MSA-01 slow the progression of motor impairment as measured by UMSARS Part 2 score?

Participants will be randomly assigned to receive MSA-01 or placebo for 12 months. They will attend regular clinic visits for safety and efficacy assessments and record their medication use and any side effects in a diary.

Inclusion: At the time of informed consent; Patients diagnosed as 'clinically established' or 'clinically probable' MSA based on the revised MSA diagnostic criteria of the Movement Disorder Society (MDS); Patients who are able to walk independently or with the use of assistive devices; Patients who are able to attend outpatient visits at the participating study site; At the start of study drug administration; Patients who are able to discontinue the use of CoQ10 supplements.

Exclusion: Patients with a known history of hypersensitivity to any component of the investigational drug; Patients who have previously participated in a clinical trial of MSA-01; Patients with severe neurological disorders, other progressive movement disorders, or cognitive impairment; Patients with severe liver disease; Pregnant women, breastfeeding women, or women who may be pregnant.

ClinicalTrials.gov NCT07446894