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Comparison · NCT02935699-c3aa30bb

Test Drug vs Control: Number of Patients Who Needed to Return to Treatment Center

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. Test Drug vs Control: Number of Patients Who Needed to Return to Treatment Center. Trial comparisons, record NCT02935699-c3aa30bb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02935699-c3aa30bb

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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 10.05510.0270.109wilson
Risk in group 20.1410.0920.209wilson
Risk difference, group 1 minus group 2-0.0856-0.16-0.0127newcombe hybrid score
Risk ratio, group 1 over group 20.3920.170.9log
Odds ratio, group 1 over group 20.3560.1440.879log
Number needed to treat, for one fewer participant with the outcome on Test Drug than on Control11.76.2679from the risk difference interval

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Test DrugJDP-205 Injection, 10 mg/mL, 1 mL~Test Drug (JDP-205): JDP-205 Injection, 10 mg/mL, 1 mL7127OG000
Group 2ControlDiphenhydramine Injection, 50 mg/mL, 1 mL~Active Control (Diphenhydramine): Diphenhydramine Injection, 50 mg/mL19135OG001

Outcome

Type
SECONDARY
Title
Number of Patients Who Needed to Return to Treatment Center
Description
Number of patients who needed to return to treatment center approximately 24 hours after discharge
Time frame
up to 24 hrs
Population
Intent To Treat Population

Source ClinicalTrials.gov

Trial

Title
Clinical Trial Comparing JDP-205 to Diphenhydramine Injection for the Treatment of Acute Urticaria
NCT number
NCT02935699
Phases
PHASE3
Conditions
Acute Urticaria
Interventions
Test Drug (JDP-205), Active Control (Diphenhydramine)
Lead sponsor
JDP Therapeutics, Inc.
Results first posted
2019-11-27

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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