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Comparison · NCT01843374-522c949a

TREMELIMUMAB vs PLACEBO: Number of Participants With Positive Anti-drug Antibodies

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. TREMELIMUMAB vs PLACEBO: Number of Participants With Positive Anti-drug Antibodies. Trial comparisons, record NCT01843374-522c949a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01843374-522c949a

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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 10.03980.02430.0646wilson
Risk in group 2000.02wilson
Risk difference, group 1 minus group 20.03980.01440.0646newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one more participant with the outcome on TREMELIMUMAB than on PLACEBO25.115.569.2from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TREMELIMUMABTremelimumab 10mg/kg15377OG001
Group 2PLACEBOPlacebo.0188OG000

Outcome

Type
SECONDARY
Title
Number of Participants With Positive Anti-drug Antibodies
Description
The immunogenicity titer is reported for samples confirmed positive for the presence of anti tremelimumab antibodies.
Time frame
Week 5
Population
Safety population

Source ClinicalTrials.gov

Trial

Title
Randomized, Double-blind Study Comparing Tremelimumab to Placebo in Subjects With Unresectable Malignant Mesothelioma
NCT number
NCT01843374
Phases
PHASE2
Conditions
Unresectable Pleural or Peritoneal Malignant Mesothelioma
Interventions
Tremelimumab, Placebo
Lead sponsor
MedImmune LLC
Results first posted
2017-08-17

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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