Evidence map›Paper›PMID 32871874›Full record

Trial reportMedicine2020

Improved Parkinsons disease motor score in a single-arm open-label trial of febuxostat and inosine.

Hirohisa Watanabe, Tatsuya Hattori, Akito Kume, Kenichiro Misu, Takashi Ito, Yu Koike, Todd A Johnson, Shigeo Kamitsuji, Naoyuki Kamatani, Gen Sobue

Registry-linked trialOpen access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07170475 (A Phase Ib Trial of Combined Febuxostat and Inosine Therapy in Patients With Parkinson's Disease), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07170475 phase1recruitingnot on this mapstarted 2025, after this paper: background citation

A Phase Ib Trial of Combined Febuxostat and Inosine Therapy in Patients With Parkinson's Disease

TypeinterventionalSponsorFujita Health UniversityRan2025 to 2026Enrolled24ConditionsParkinson's Disease (PD)ArmsFebuxostat, Inosine
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. A qPCR-based approach targeting the microbial gene markerJournal of Parkinson's disease · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Uric Acid in Parkinson's Disease: What Is the Connection?Movement disorders : official journal of the Movement Disorder Society · 2022
    Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Hirohisa WatanabeNagoya University Graduate School of Medicine, Brain and Mind Research Center, Nagoya.
Tatsuya HattoriHonmachi Clinic, Naka-ku.
Akito KumeKUME Clinic, Mizuho-ku, Nagoya.
Kenichiro MisuMISU Clinic, Miyoshi.
Takashi ItoSaishukan Hospital, Kitanagoya, Aichi.
Yu KoikeOASIS Clinic, Ushiku, Ibaraki.
Todd A JohnsonStaGen Co., Ltd., Taito-ku, Tokyo, Japan.ORCID 0000-0003-3377-6692
Shigeo KamitsujiStaGen Co., Ltd., Taito-ku, Tokyo, Japan.
Naoyuki KamataniStaGen Co., Ltd., Taito-ku, Tokyo, Japan.
Gen SobueNagoya University Graduate School of Medicine, Brain and Mind Research Center, Nagoya.
StaGen (Japan) · JPFujita Health University · JPJA Shizuoka Koseiren ENSHU hospital · JPMizuho (Japan) · JPNagoya University · JPOASIS Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCellular energetics play an important role in Parkinsons disease etiology, but no treatments directly address this deficiency. Our past research showed that treatment with febuxostat and inosine increased blood hypoxanthine and ATP in healthy adults, and a preliminary trial in 3 Parkinson's disease patients suggested some symptomatic improvements with no adverse effects.

methodsTo examine the efficacy on symptoms and safety in a larger group of Parkinsons disease patients, we conducted a single-arm, open-label trial at 5 Japanese neurology clinics and enrolled thirty patients (nmales = 11; nfemales = 19); 26 patients completed the study (nmales = 10; nfemales = 16). Each patient was administered febuxostat 20 mg and inosine 500 mg twice-per-day (after breakfast and dinner) for 8 weeks. The primary endpoint was the difference of MDS-UPDRS Part III score immediately before and after 57 days of treatment.

resultsSerum hypoxanthine concentrations were raised significantly after treatment (Pre = 11.4 μM; Post = 38.1 μM; P < .0001). MDS-UPDRS Part III score was significantly lower after treatment (Pre = 28.1 ± 9.3; Post = 24.7 ± 10.8; mean ± SD; P = .0146). Sixteen adverse events occurred in 13/29 (44.8%) patients, including 1 serious adverse event (fracture of the second lumbar vertebra) that was considered not related to the treatment.

conclusionsThe results of this study suggest that co-administration of febuxostat and inosine is relatively safe and effective for improving symptoms of Parkinsons disease patients. Further controlled trials need to be performed to confirm the symptomatic improvement and to examine the disease-modifying effect in long-term trials.

Indexed as

Adenosine TriphosphateAdministration, OralAgedCase-Control StudiesDrug Therapy, CombinationFebuxostatFemaleGout SuppressantsHumansHypoxanthineInosineJapanMaleMiddle AgedNervous System DiseasesParkinson DiseaseAdenosine TriphosphateFebuxostatGout SuppressantsHypoxanthineInosineXanthine Dehydrogenase

Identifiers

PMID32871874
PMCPMC7458241
OpenAlexW3081504018

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.