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Trial · NCT07880379

MK-0947 PN-002: An Open-label Study to Evaluate Brain α-synuclein Deposition Using Positron Emission Tomography (PET) and [¹⁸F]MK-0947 in Participants With Parkinson's Disease (PD)

NCT07880379, Phase 1, Recruiting, XingImaging, LLC

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. MK-0947 PN-002: An Open-label Study to Evaluate Brain α-synuclein Deposition Using Positron Emission Tomography (PET) and [¹⁸F]MK-0947 in Participants With Parkinson's Disease (PD). Trials, record NCT07880379. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07880379

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
MK-0947 PN-002: An Open-label Study to Evaluate Brain α-synuclein Deposition Using Positron Emission Tomography (PET) and [¹⁸F]MK-0947 in Participants With Parkinson's Disease (PD)
NCT number
NCT07880379
Status
Recruiting
Phases
Phase 1
Enrollment
18 participants, estimated
Lead sponsor
XingImaging, LLC
Conditions
Parkinsons Disease (PD), Healthy Elderly Volunteers
Interventions
[¹⁸F]MK-0947
First posted
2026-10-19
Last updated
2026-10-19

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBrain uptake of [¹⁸F]MK-0947From imaging to follow up, an average of 1 yearTo visually and quantitatively assess brain uptake of \[¹⁸F\]MK-0947 as a PET radioligand for alpha-synuclein pathology (e.g. Standard Uptake Value Ratios (SUVR)).
PrimarySafety of [¹⁸F]MK-0947: Incidence of Adverse EventsFrom enrollment to follow up, an average of 1 yearIncidence of adverse events (AEs) following administration
PrimaryStandard Uptake Value Ratios (SUVR)From imaging to follow up, an average of 1 yearTo evaluate Standard Uptake Value Ratios (SUVR) in relevant brain regions from \[18F\]MK-0947 PET in PD and healthy participants.
SecondaryBinding Comparison of [¹⁸F]MK-0947 PD and Healthy ElderlyFrom imaging to follow up, an average of 1 year
To compare the binding of \[¹⁸F\]MK-0947 in the brain of participants with PD with similarly age-matched HE via evaluation of suitable regional quantification parameter (e.g., SUVR) in regions known to be involved in α-synuclein pathology and regions known to not be involved in such pathology.
SecondaryBinding Comparison - CameraFrom imaging to follow up, an average of 1 yearTo compare the binding of \[¹⁸F\]MK-0947 in the brain of participants with PD with that in HE using the standard- and NX- PET

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07880379

GET https://conductscience.org/api/trials/v1/NCT07880379/registered