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Comparison · NCT03575052-sae

Pimavanserin 34 mg vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Pimavanserin 34 mg vs Placebo: serious adverse events. Trial comparisons, record NCT03575052-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03575052-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.02040.01040.0397wilson
Risk in group 20.01530.007030.033wilson
Risk difference, group 1 minus group 20.0051-0.01520.0261newcombe hybrid score
Risk ratio, group 1 over group 21.330.4673.81log
Odds ratio, group 1 over group 21.340.4613.9log
Number needed to harm, for one more participant with a serious adverse event on Pimavanserin 34 mg than on Placebo196from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Pimavanserin 34 mgPimavanserin 34 mg (administered as 2 x 17 mg capsules) once daily8392EG001
Group 2PlaceboPimavanserin matching placebo (administered as 2 capsules) once daily6392EG000

Harm

What it counts
Total, serious adverse events
Time frame
Treatment period (8 weeks) and follow-up period (30 days): total of approximately 15 weeks

Source ClinicalTrials.gov

Trial

Title
A Safety Study of Pimavanserin in Adult and Elderly Subjects Experiencing Neuropsychiatric Symptoms Related to Neurodegenerative Disease
NCT number
NCT03575052
Phases
PHASE3
Conditions
Neuropsychiatric Symptoms Related to Neurodegenerative Disease
Interventions
Pimavanserin, Placebo
Lead sponsor
ACADIA Pharmaceuticals Inc.
Results first posted
2024-12-31

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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