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Comparison · NCT04221230-83151be4

NMRA-335140 vs Placebo: Number of Participants With Clinically Significant Changes in Vital Parameters

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. NMRA-335140 vs Placebo: Number of Participants With Clinically Significant Changes in Vital Parameters. Trial comparisons, record NCT04221230-83151be4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04221230-83151be4

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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 1000.0363wilson
Risk in group 2000.0363wilson
Risk difference, group 1 minus group 20-0.03630.0363newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treatfrom the risk difference intervalthe two groups' risks are equal

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1NMRA-335140Participants were randomized in a 1:1 ratio and received 80 milligrams (mg) of NMRA-335140 once daily orally.0102OG000
Group 2PlaceboParticipants were randomized in a 1:1 ratio and received matching placebo once daily orally.0102OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Clinically Significant Changes in Vital Parameters
Description
The following vital parameters were analyzed: diastolic blood pressure, systolic blood pressure, temperature, heart rate and respiratory rate.
Time frame
Up to 8 Weeks
Population
Safety Population.

Source ClinicalTrials.gov

Trial

Title
Study in Major Depressive Disorder With NMRA-335140 (BTRX-335140) vs Placebo
NCT number
NCT04221230
Phases
PHASE2
Conditions
Major Depressive Disorder
Interventions
NMRA-335140, Placebo
Lead sponsor
Neumora Therapeutics, Inc.
Results first posted
2025-05-29

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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