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Comparison · NCT01151423-e3ac1883

Caplacizumab vs Placebo: Number and Percentage of Subjects With Relapse of TTP

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. Caplacizumab vs Placebo: Number and Percentage of Subjects With Relapse of TTP. Trial comparisons, record NCT01151423-e3ac1883. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01151423-e3ac1883

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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 10.3060.180.469wilson
Risk in group 20.07690.02650.203wilson
Risk difference, group 1 minus group 20.2290.05060.399newcombe hybrid score
Risk ratio, group 1 over group 23.971.213.1log
Odds ratio, group 1 over group 25.281.3420.9log
Number needed to treat, for one more participant with the outcome on Caplacizumab than on Placebo4.372.519.8from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CaplacizumabCaplacizumab 10 mg once daily1136OG000
Group 2PlaceboPlacebo once daily339OG001

Outcome

Type
SECONDARY
Title
Number and Percentage of Subjects With Relapse of TTP
Description
Number and percentage of subjects with relapse of TTP (defined as de novo TTP event that occurred later than 30 days after the last daily PE) was evaluated.
Time frame
Later than 30 days after the last daily PE
Population
ITT Population

Source ClinicalTrials.gov

Trial

Title
Study to Assess Efficacy and Safety of Anti-von Willebrand Factor (vWF) Nanobody in Patients With Acquired Thrombotic Thrombocytopenic Purpura (aTTP)
NCT number
NCT01151423
Phases
PHASE2
Conditions
Acquired Thrombotic Thrombocytopenic Purpura
Interventions
Caplacizumab, Placebo
Lead sponsor
Ablynx, a Sanofi company
Results first posted
2019-05-29

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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