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Patients Treated With ABL vs Patients Treated With TPTD: Number of Participants With Hip Fracture

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

Measures 6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.01020.008450.0122wilsonClinicalTrials.gov
Risk in group 20.01130.009520.0135wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00118-0.003930.00156newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.8960.6951.15logClinicalTrials.gov
Odds ratio, group 1 over group 20.8950.6931.16logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Patients Treated With ABL than on Patients Treated With TPTD848from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Patients Treated With ABLPatients who filled ≥ 1 prescription for ABL (TYMLOS) as their index medication during the identification period.11211,027OG000ClinicalTrials.gov
Group 2Patients Treated With TPTDPatients who filled ≥ 1 prescription for TPTD (Forteo) as their index medication during the identification period.12511,027OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeOTHER_PRE_SPECIFIEDClinicalTrials.gov
TitleNumber of Participants With Hip FractureClinicalTrials.gov
Description
The date of the first prescription claim for either abaloparatide or teriparatide during the identification period was considered the index date. A claims-based algorithm with high specificity for fracture site was used to identify osteoporosis related fractures. Patients were followed up for 18 months after their index date, plus 30 days follow-up or until their first hip fracture event or hospital death, whichever came first.
ClinicalTrials.gov
Time frameFrom index date up to 19 monthsClinicalTrials.gov
PopulationAll patients meeting the study inclusion/exclusion criteria and selected after PS-matching.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleReal-world Effectiveness and Cardiovascular Safety Study of Abaloparatide in Postmenopausal WomenClinicalTrials.gov
NCT numberNCT04974723ClinicalTrials.gov
PhasesClinicalTrials.gov
ConditionsOsteoporosis, PostmenopausalClinicalTrials.gov
InterventionsAbaloparatide, TeriparatideClinicalTrials.gov
Lead sponsorRadius Health, Inc.ClinicalTrials.gov
Results first posted2024-04-19ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT04974723?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.