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Study on efficacy and safety as well as on the changes in blood purine compounds by the treatment of patients with amyotrophic lateral sclerosis with febuxostat and inosine in combination.

Study on efficacy and safety as well as on the changes in blood purine compounds by the treatment of patients with amyotrophic lateral sclerosis with febuxostat and inosine in combination. - Effect of febuxostat and inosine on amyotrophic lateral sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029308
Enrollment
3
Registered
2018-09-30
Start date
2017-07-18
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amyotrophic lateral sclerosis

Interventions

Febuxostat 20 mg, Inosine 500 mg, twice a day for 14 days

Sponsors

Teikyo University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Japanese patients with 20 to 80 years of age who are the outpatients of Teikyo University Hospital 2. Patients who have been diagnosed as amyotrophic lateral sclerosis

Exclusion criteria

Exclusion criteria: 1. Subject who has or had hypersensitivity, idiosyncracy (allergy) to drug. 2. Subjects taking azathioprine or mercaptopurine 3. Subject who has or had renal function disorder. 4. Subject with a history of gout, hyperuricemia or urolithiasis. 5. Patients who changed therapeutic drugs and treatment methods within 1 month before administration of test drugs 6. Subject who was judged not to be appropriate by the principal investigator or sub investigators by other reasons.

Design outcomes

Primary

MeasureTime frame
Difference of ALSFRS-R between before and after the treatment

Countries

Japan

Contacts

Public ContactFumiaki Saito

Teikyo University Department of neurology, Faculty of Medicine

f-saito@med.teikyo-u.ac.jp03-3964-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026