ClinicalTrials.gg
Not yet recruitingNCT07825402Updated Sep 17, 2026

A Trial of ONO-2808 in Participants With the Parkinsonian Subtype of Multiple System Atrophy (MSA-P)

A Phase 3 interventional study of ONO-2808 and Placebo in Multiple System Atrophy, Parkinson Variant, sponsored by Ono Pharmaceutical Co., Ltd.. Not yet recruiting. Open to participants aged 30 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-17.

Sponsored by Ono Pharmaceutical Co., Ltd. · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
486
Allocation
Randomized
Ages
30 Years to 80 Years
Sex
All
01

Study summary

The main goal of this clinical trial is to learn if ONO-2808 works to treat adults with the Parkinsonian subtype of Multiple System Atrophy (MSA-P). Researchers will compare ONO-2808 to a placebo (a look-alike substance that contains no drug) to see if ONO-2808 works to treat MSA-P.

Participants will:

  • Take ONO-2808 or placebo orally for up to 48 weeks
  • Make visits to the clinic for checkups and tests
  • Answer questions about their health throughout the trial.
02

Conditions studied

  • Multiple System Atrophy, Parkinson Variant

Keywords

  • MSA-P
  • Parkinson's
  • Parkinsonian Subtype of
  • Parkinsonism
  • MSA
  • Multiple System Atrophy
  • Movement Disorder
03

In context

Multiple System Atrophy

207 studies on the registry are indexed under Multiple System Atrophy; 73 are open to participants now.

This study's planned enrollment of 486 is above the median of 41 across 134 interventional studies indexed under Multiple System Atrophy.

Browse Multiple System Atrophy studies →

Lead sponsor

Ono Pharmaceutical Co., Ltd. is the lead sponsor of 49 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Key Inclusion Criteria:

  • Participants with a diagnosis of clinically established or clinically probable MSA-P according to the 2022 Movement Disorder Society (MDS) criteria for MSA diagnosis.
  • Participants in the early stages of the disease, defined as a maximum of 5 years since the onset of one of the following symptoms associated with MSA-P:

    • Parkinsonism
    • Orthostatic hypotension
    • Urinary dysautonomia
  • Participants with an anticipated survival of at least 3 years in the opinion of the Investigator.
  • Participants who are able to ambulate without the assistance of another person, defined as the ability to take at least 10 steps and then to turn around and walk at least another 10 steps. Use of assistive devices (eg, walker or cane) is allowed.
  • Ability to swallow oral medication and willingness to adhere to the study drug regimen.
  • Normal range of laboratory values at screening and baseline, especially liver function tests.
  • Participants receiving treatment (including chronic medications, and herbal or dietary supplements) for symptoms associated with MSA must be on a stable dosage for at least 60 days prior to randomization based on the judgment of the Investigator. Participants must not initiate new treatment within 60 days prior to randomization.

Key Exclusion Criteria:

  • Participants with the cerebellar subtype of MSA according to the 2022 MDS criteria for MSA diagnosis.
  • Female participants who are pregnant, planning to become pregnant during the study, or breastfeeding.
  • Participants with a or unstable medical or surgical condition other than MSA-P that, in the opinion of the Investigator, might preclude safe completion of the study or might affect the results of the study (eg, pulmonary, cardiovascular [including bradyarrhythmia], macular edema, and significant renal or hepatic dysfunction).
  • Neurological diseases/disorders other than MSA-P, such as Parkinson's disease, dementia with Lewy bodies, essential tremor, progressive supranuclear palsy, spinocerebellar ataxia, spastic paraparesis, corticobasal degeneration, or vascular, normal pressure hydrocephalus, pharmacological, or postencephalitic parkinsonism.
  • Any abnormalities, other than MSA, found on the centrally read brain MRI that, in the opinion of the Investigator, may constitute a confounder for the study or preclude safe participation.
  • Participants with documented liver diseases, cirrhosis, prior drug-induced liver injury (DILI), or ascites or symptoms and signs of encephalopathy due to hepatic dysfunction.

Other protocol-defined inclusion and exclusion criteria apply.

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
486 participants (estimated)

Study arms

  • Experimental
    ONO-2808 Low Dose

    Drug: ONO-2808

  • Experimental
    ONO-2808 High Dose

    Drug: ONO-2808

  • Placebo comparator
    Placebo

    Other: Placebo

Interventions

  • ONO-2808 will be administered to participants orally once daily for 48 weeks.

  • OtherPlacebo

    Matching placebo will be administered to participants orally once daily for 48 weeks.

06

What researchers measure

Primary outcomes

  1. Change from Baseline in modified United Multiple System Atrophy Rating Scale (mUMSARS) Part I (excluding Item 11) with Collapsed Scoring (0-3)

    Time frame: Baseline, Week 48

Secondary outcomes

  1. Change from Baseline in Multiple System Atrophy Quality of Life Scale (MSA-QoL) Motor Subscale Score

    Time frame: Baseline, Week 48

  2. Change from Baseline in Magnetic Resonance Imaging (MRI) Volumetric Assessments

    Time frame: Baseline, Week 48

  3. Change from Baseline in Total United Multiple System Atrophy Rating Scale (UMSARS) Score (Part I and Part II, all items)

    Time frame: Baseline, Week 48

  4. Change from Baseline in mUMSARS Score

    Time frame: Baseline, Week 48

  5. Change from Baseline in MSA-QoL Total Score

    Time frame: Baseline, Week 48

  6. Change from Baseline in Patient Global Impression of Change (PGI-C) Score

    Time frame: Baseline, Week 48

  7. Change from Baseline in Patient Global Impression of Severity (PGI-S) Score

    Time frame: Baseline, Week 48

  8. Change from Baseline in Clinical Global Impression of Change (CGI-C) Score

    Time frame: Baseline, Week 48

  9. Change from Baseline in Clinical Global Impression of Severity (CGI-S) Score

    Time frame: Baseline, Week 48

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jan 2027; primary completion for Oct 2029, 33 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 13, 2026
First posted
Sep 17, 2026
StartEst.
Jan 2027
Primary completionEst.
Oct 2029
CompletionEst.
Oct 2029
Last update
Sep 17, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07825402
Responsible party
Sponsor
First posted
Sep 17, 2026
Start date
Jan 2027 (estimated)
Primary completion
Oct 2029 (estimated)
Completion
Oct 2029 (estimated)
Last update
Sep 17, 2026

Study contacts

Clinical Team
Contact
clinicaltrials@deciphera.com
888-724-3274
Clinical Team
study director · Ono Pharmaceutical Co., Ltd.

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Studies of the drug tested here: ONO-2808

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