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Trial · NCT01485172

Results by group66

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline (BL) in Unified Parkinson Disease (PD) Rating Scale (UPDRS) Motor ScoreTreatment Group A: Placebo-1.9195% Confidence Interval -4.15 to 0.34Score on a scale
Change From Baseline (BL) in Unified Parkinson Disease (PD) Rating Scale (UPDRS) Motor ScoreTreatment Group B: 2 mg/Day-1.5895% Confidence Interval -5.02 to 1.86Score on a scale
Change From Baseline (BL) in Unified Parkinson Disease (PD) Rating Scale (UPDRS) Motor ScoreTreatment Group C: 4 mg/Day-2.7695% Confidence Interval -5.04 to -0.49Score on a scale
Change From Baseline (BL) in Unified Parkinson Disease (PD) Rating Scale (UPDRS) Motor ScoreTreatment Group D: 8 mg/Day-4.3195% Confidence Interval -6.48 to -2.15Score on a scale
Change From Baseline (BL) in Unified Parkinson Disease (PD) Rating Scale (UPDRS) Motor ScoreTreatment Group E: 12 mg/Day-4.0795% Confidence Interval -6.32 to -1.82Score on a scale
Change From Baseline (BL) in Unified Parkinson Disease (PD) Rating Scale (UPDRS) Motor ScoreTreatment Group F: 24 mg/Day-2.8395% Confidence Interval -6.61 to 0.95Score on a scale
Number of Participants With a >=5 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group A: Placebo9Participants
Number of Participants With a >=5 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group B: 2 mg/Day6Participants
Number of Participants With a >=5 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group C: 4 mg/Day14Participants
Number of Participants With a >=5 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group D: 8 mg/Day16Participants
Number of Participants With a >=5 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group E: 12 mg/Day19Participants
Number of Participants With a >=5 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group F: 24 mg/Day5Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group A: Placebo5Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group B: 2 mg/Day3Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group C: 4 mg/Day7Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group D: 8 mg/Day7Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group E: 12 mg/Day9Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Motor ScoreTreatment Group F: 24 mg/Day2Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Parts II and III CombinedTreatment Group A: Placebo6Participants
Number of Participants With a >=10 Points Reduction From Baseline in UPDRS Parts II and III CombinedTreatment Group B: 2 mg/Day3Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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