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Comparison · NCT04222712-ee522ed1

TRS01 Low Dose vs TRS01 High Dose: Assessment of Both Systemic and Ocular 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. TRS01 Low Dose vs TRS01 High Dose: Assessment of Both Systemic and Ocular Adverse Events. Trial comparisons, record NCT04222712-ee522ed1. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04222712-ee522ed1

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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 10.250.07150.591wilson
Risk in group 20.6250.3060.863wilson
Risk difference, group 1 minus group 2-0.375-0.6730.0919newcombe hybrid score
Risk ratio, group 1 over group 20.40.1071.49log
Odds ratio, group 1 over group 20.20.02341.71log
Number needed to treat, for one fewer participant with the outcome on TRS01 Low Dose than on TRS01 High Dose2.67from 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 1TRS01 Low DoseTRS01 eye drops: Dosed four times a day (QID)28OG000
Group 2TRS01 High DoseTRS01 eye drops: Dosed four times a day (QID)58OG001

Outcome

Type
PRIMARY
Title
Assessment of Both Systemic and Ocular Adverse Events
Description
Number of patients experiencing Adverse Events during the study
Time frame
10 weeks
Population

Source ClinicalTrials.gov

Trial

Title
A Study to Evaluate TRS01 Eye Drops in Participants With Active Non-infectious Anterior Uveitis
NCT number
NCT04222712
Phases
PHASE1, PHASE2
Conditions
Non-infectious Anterior Uveitis
Interventions
TRS01 eye drops, TRS01 eye drops
Lead sponsor
Tarsier Pharma
Results first posted
2023-10-05

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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