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Comparison · NCT02746991-sae

FAI Insert vs Sham Injection: 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. FAI Insert vs Sham Injection: serious adverse events. Trial comparisons, record NCT02746991-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02746991-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 10.2080.140.297wilson
Risk in group 20.1350.06680.253wilson
Risk difference, group 1 minus group 20.0733-0.06280.185newcombe hybrid score
Risk ratio, group 1 over group 21.540.7033.39log
Odds ratio, group 1 over group 21.690.6664.28log
Number needed to harm, for one more participant with a serious adverse event on FAI Insert than on Sham Injection13.6from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: sham.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1FAI InsertFAI Insert Group21101EG001
Group 2Sham InjectionPlacebo Injection752EG000

Harm

What it counts
Total, serious adverse events
Time frame
36 months. All Adverse Event (AE)s will be evaluated from their onset until resolution, stabilization, last day of participation in the study of the patient or the last day of the study, whichever is first.

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy Study of a FAI Insert in Subjects With Chronic Non-infectious Posterior Uveitis
NCT number
NCT02746991
Phases
PHASE3
Conditions
Posterior Uveitis, Intermediate Uveitis, Panuveitis
Interventions
Sham Injection, FAI Insert
Lead sponsor
EyePoint Pharmaceuticals, Inc.
Results first posted
2020-07-07

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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