Comparison · NCT04944290-sae
Perrigo Active vs Reference Active: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Perrigo Active vs Reference Active: serious adverse events. Trial comparisons, record NCT04944290-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04944290-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.00905 | 0.00249 | 0.0324 | wilson | |
| Risk in group 2 | 0.0177 | 0.0069 | 0.0446 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00865 | -0.0364 | 0.0171 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.511 | 0.0946 | 2.76 | log | |
| Odds ratio, group 1 over group 2 | 0.507 | 0.0919 | 2.8 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Perrigo Active than on Reference Active | 116 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Perrigo Active | Brinzolamide/brimonidine ophthalmic suspension: Test product | 2 | 221 | EG000 |
| Group 2 | Reference Active | Simbrinza 0.2%/1% Ophthalmic Suspension: Reference product | 4 | 226 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Day 1 to Day 46
Source ClinicalTrials.gov
Trial
- Title
- To Compare the Efficacy and Safety of Perrigo's Product to an FDA Approved Product for the Treatment of Glaucoma or Ocular Hypertension in Both Eyes
- NCT number
- NCT04944290
- Phases
- PHASE3
- Conditions
- Glaucoma, Open-Angle, Ocular Hypertension
- Interventions
- Brinzolamide/brimonidine ophthalmic suspension, Simbrinza 0.2%/1% Ophthalmic Suspension
- Lead sponsor
- Padagis LLC
- Results first posted
- 2025-04-02
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT04944290?tab=results
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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