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Comparison · NCT02865915-sae

MLE4901 Treatment Arm vs Placebo Treatment Arm: 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. MLE4901 Treatment Arm vs Placebo Treatment Arm: serious adverse events. Trial comparisons, record NCT02865915-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02865915-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 10.03330.005910.167wilson
Risk in group 200.00000000000000001390.133wilson
Risk difference, group 1 minus group 20.0333-0.1030.167newcombe 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 harm, for one more participant with a serious adverse event on MLE4901 Treatment Arm than on Placebo Treatment Arm30from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1MLE4901 Treatment ArmTreatment with 1 tablet of MLE4901 self-administered twice daily \[80% treated with dose of 40 mg twice daily\]130EG001
Group 2Placebo Treatment ArmTreatment with 1 matching placebo tablet self-administered twice daily025EG000

Harm

What it counts
Total, serious adverse events
Time frame
During the time period between enrollment of the first subject until the data lock date, approximately 9 months.

Source ClinicalTrials.gov

Trial

Title
MLE4901 vs. Placebo for the Treatment of PCOS
NCT number
NCT02865915
Phases
PHASE2
Conditions
Polycystic Ovary Syndrome (PCOS)
Interventions
MLE4901, Placebo
Lead sponsor
Millendo Therapeutics US, Inc.
Results first posted
2020-06-16

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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