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Comparison · NCT00936897-sae

Ibandronate 150 mg PO QM vs Denosumab 60 mg SC Q6M: serious 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. Ibandronate 150 mg PO QM vs Denosumab 60 mg SC Q6M: serious adverse events. Trial comparisons, record NCT00936897-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00936897-sae

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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 10.05370.03570.0799wilson
Risk in group 20.09490.07020.127wilson
Risk difference, group 1 minus group 2-0.0412-0.0781-0.00519newcombe hybrid score
Risk ratio, group 1 over group 20.5650.3410.936log
Odds ratio, group 1 over group 20.5410.3150.93log
Number needed to treat, for one fewer participant with a serious adverse event on Ibandronate 150 mg PO QM than on Denosumab 60 mg SC Q6M24.312.8193from 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 1Ibandronate 150 mg PO QMIbandronate 150 mg oral monthly22410EG000
Group 2Denosumab 60 mg SC Q6MDenosumab 60 mg subcutaneous once every 6 months39411EG001

Harm

What it counts
Total, serious adverse events
Time frame
12 months

Source ClinicalTrials.gov

Trial

Title
A Study to Evaluate the Safety and Efficacy of Denosumab and Ibandronate in Postmenopausal Women Sub-Optimally Treated With Daily or Weekly Bisphosphonates
NCT number
NCT00936897
Phases
PHASE3
Conditions
Postmenopausal Osteoporosis
Interventions
Ibandronate, Denosumab
Lead sponsor
Amgen
Results first posted
2012-11-29

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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