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Comparison · NCT03450629-sae

PDP-716 vs Brimonidine Tartrate Ophthalmic Solution: 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. PDP-716 vs Brimonidine Tartrate Ophthalmic Solution: serious adverse events. Trial comparisons, record NCT03450629-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03450629-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 10.002970.0005240.0166wilson
Risk in group 20.00880.0030.0255wilson
Risk difference, group 1 minus group 2-0.00583-0.02280.009newcombe hybrid score
Risk ratio, group 1 over group 20.3370.03533.23log
Odds ratio, group 1 over group 20.3350.03473.24log
Number needed to treat, for one fewer participant with a serious adverse event on PDP-716 than on Brimonidine Tartrate Ophthalmic Solution172from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PDP-716Brimonidine Tartrate Ophthalmic Suspension1337EG000
Group 2Brimonidine Tartrate Ophthalmic SolutionBrimonidine Tartrate Ophthalmic Solution: Three Times Brimonidine Tartrate Ophthalmic Solution3341EG001

Harm

What it counts
Total, serious adverse events
Time frame
12 weeks

Source ClinicalTrials.gov

Trial

Title
Evaluation of Safety and Efficacy of PDP-716
NCT number
NCT03450629
Phases
PHASE3
Conditions
Open Angle Glaucoma, Ocular Hypertension
Interventions
Brimonidine Tartrate Ophthalmic Suspension, Brimonidine Tartrate Ophthalmic Solution
Lead sponsor
Sun Pharma Advanced Research Company Limited
Results first posted
2022-02-15

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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