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Comparison · NCT03169972-b5e796c1

Previously Treated Patients (PTPs) vs Previously Untreated Patients (PUPs): Number of Participants Who Discontinued the Use of Study Drug

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. Previously Treated Patients (PTPs) vs Previously Untreated Patients (PUPs): Number of Participants Who Discontinued the Use of Study Drug. Trial comparisons, record NCT03169972-b5e796c1. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03169972-b5e796c1

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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 10.08130.04480.143wilson
Risk in group 20.4170.1930.68wilson
Risk difference, group 1 minus group 2-0.335-0.602-0.104newcombe hybrid score
Risk ratio, group 1 over group 20.1950.07970.478log
Odds ratio, group 1 over group 20.1240.03320.463log
Number needed to treat, for one fewer participant with the outcome on Previously Treated Patients (PTPs) than on Previously Untreated Patients (PUPs)2.981.669.66from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Previously Treated Patients (PTPs)
Participants with hemophilia A who received Recombinant Factor VIII (FVIII) PEGylated (ADYNOVATE) intravenous Infusion as part of a routine medical care. Participants in this group were previously treated patients with Factor VIII deficiency (PTPs) who had 4 or more exposure days to other Factor VIII (FVIII) products.
10123OG000
Group 2Previously Untreated Patients (PUPs)
Participants with hemophilia A who received Recombinant Factor VIII (FVIII) PEGylated (ADYNOVATE) intravenous Infusion as part of a routine medical care. Participants in this group were previously untreated patients with Factor VIII deficiency (PUPs) who had 3 or less previous exposure days to other Factor VIII (FVIII) products.
512OG001

Outcome

Type
PRIMARY
Title
Number of Participants Who Discontinued the Use of Study Drug
Description
Number of previously treated patients (PTPs) and previously untreated patients (PUPs) who discontinued the use of ADYNOVATE were reported.
Time frame
Throughout the study participation period: 1 year for previously treated patients for PTPs and 2 years for previously untreated patients for PUPs
Population
Safety Analysis Set, The safety analysis set was defined as all participants who completed the survey.

Source ClinicalTrials.gov

Trial

Title
ADYNOVATE Drug Use-Results Survey
NCT number
NCT03169972
Phases
Conditions
Hemophilia A
Interventions
ADYNOVATE
Lead sponsor
Takeda
Results first posted
2025-02-04

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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