Trial Outcomes & Findings for Real-world Effectiveness and Cardiovascular Safety Study of Abaloparatide in Postmenopausal Women (NCT NCT04974723)
NCT ID: NCT04974723
Last Updated: 2024-04-19
Results Overview
A nonvertebral fracture is any fragility fracture at the hip, pelvis, femur, ankle, shoulder (including shoulder, humerus, clavicle), radius/ulna, wrist, or tibia/fibula. 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 for up to 18 months after their index date, plus 30 days follow-up or until their first nonvertebral fracture event or hospital death, whichever came first.
COMPLETED
22054 participants
From index date up to 19 months
2024-04-19
Participant Flow
Propensity score (PS) matching was used to create treatment cohorts. Patients were matched using an extensive list of indicators of disease severity and fracture risk, including fracture and treatment history, as well as conditions associated with increased risk of fall and the requirement for treatments associated with poor bone health or quality.
Participant milestones
| Measure |
Patients Treated With Abaloparatide
Patients who filled ≥ 1 prescription for Abaloparatide (ABL) (TYMLOS) as their index medication during the identification period.
|
Patients Treated With Teriparatide
Patients who filled ≥ 1 prescription for Teriparatide (TPTD) (Forteo) as their index medication during the identification period.
|
|---|---|---|
|
Overall Study
STARTED
|
11027
|
11027
|
|
Overall Study
COMPLETED
|
11027
|
11027
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Real-world Effectiveness and Cardiovascular Safety Study of Abaloparatide in Postmenopausal Women
Baseline characteristics by cohort
| Measure |
Patients Treated With ABL
n=11027 Participants
Patients who filled ≥ 1 prescription for ABL (TYMLOS) as their index medication during the identification period.
|
Patients Treated With TPTD
n=11027 Participants
Patients who filled ≥ 1 prescription for TPTD (Forteo) as their index medication during the identification period.
|
Total
n=22054 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
67.3 years
STANDARD_DEVIATION 8.35 • n=99 Participants
|
67.4 years
STANDARD_DEVIATION 8.39 • n=107 Participants
|
67.38 years
STANDARD_DEVIATION 8.37 • n=206 Participants
|
|
Sex: Female, Male
Female
|
11027 Participants
n=99 Participants
|
11027 Participants
n=107 Participants
|
22054 Participants
n=206 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Race/Ethnicity, Customized
African American
|
144 Participants
n=99 Participants
|
150 Participants
n=107 Participants
|
294 Participants
n=206 Participants
|
|
Race/Ethnicity, Customized
Asian
|
100 Participants
n=99 Participants
|
104 Participants
n=107 Participants
|
204 Participants
n=206 Participants
|
|
Race/Ethnicity, Customized
White
|
4137 Participants
n=99 Participants
|
4262 Participants
n=107 Participants
|
8399 Participants
n=206 Participants
|
|
Race/Ethnicity, Customized
Hispanic
|
646 Participants
n=99 Participants
|
531 Participants
n=107 Participants
|
1177 Participants
n=206 Participants
|
|
Race/Ethnicity, Customized
Other
|
127 Participants
n=99 Participants
|
107 Participants
n=107 Participants
|
234 Participants
n=206 Participants
|
|
Race/Ethnicity, Customized
Unknown
|
5873 Participants
n=99 Participants
|
5873 Participants
n=107 Participants
|
11746 Participants
n=206 Participants
|
PRIMARY outcome
Timeframe: From index date up to 19 monthsPopulation: All patients meeting the study inclusion/exclusion criteria and selected after PS-matching.
A nonvertebral fracture is any fragility fracture at the hip, pelvis, femur, ankle, shoulder (including shoulder, humerus, clavicle), radius/ulna, wrist, or tibia/fibula. 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 for up to 18 months after their index date, plus 30 days follow-up or until their first nonvertebral fracture event or hospital death, whichever came first.
Outcome measures
| Measure |
Patients Treated With ABL
n=11027 Participants
Patients who filled ≥ 1 prescription for ABL (TYMLOS) as their index medication during the identification period.
|
Patients Treated With TPTD
n=11027 Participants
Patients who filled ≥ 1 prescription for TPTD (Forteo) as their index medication during the identification period.
|
|---|---|---|
|
Number of Participants With a Nonvertebral Fracture
|
313 Participants
|
333 Participants
|
SECONDARY outcome
Timeframe: From index date up to 19 monthsPopulation: All patients meeting the study inclusion/exclusion criteria and selected after PS-matching.
Cardiovascular safety was evaluated based only on events occurring from the beginning of the index period through 19 months. The date of the first prescription claim for either abaloparatide or teriparatide during the identification period was considered the index date. Cardiovascular events (MI and stroke) were defined as the first post-index incidence recorded on a hospital claim or physician claim. A validated claims-based algorithm was used to identify deaths, based on hospital discharge status, that are likely to be caused by cardiovascular events. Patients were followed for up to 18 months while on treatment plus 30 days follow-up, or until their first cardiovascular event (MI or stroke) or hospital death, whichever came first.
Outcome measures
| Measure |
Patients Treated With ABL
n=11027 Participants
Patients who filled ≥ 1 prescription for ABL (TYMLOS) as their index medication during the identification period.
|
Patients Treated With TPTD
n=11027 Participants
Patients who filled ≥ 1 prescription for TPTD (Forteo) as their index medication during the identification period.
|
|---|---|---|
|
Number of Participants With Composite Endpoint of Nonfatal Myocardial Infarction (MI), Nonfatal Stroke, or In-hospital Cardiovascular Death
|
221 Participants
|
211 Participants
|
SECONDARY outcome
Timeframe: From index date up to 19 monthsPopulation: All patients meeting the study inclusion/exclusion criteria and selected after PS-matching.
Cardiovascular safety was evaluated based only on events occurring from the beginning of the index period through 19 months. The date of the first prescription claim for either abaloparatide or teriparatide during the identification period was considered the index date. Cardiovascular events (MI, stroke, and heart failure) were defined as the first post-index incidence recorded on a hospital claim or physician claim. A validated claims-based algorithm was used to identify deaths, based on hospital discharge status, that are likely to be caused by cardiovascular events. Patients were followed for up to 18 months while on treatment plus 30 days follow-up, or until their first cardiovascular event (MI, stroke, or heart failure) or hospital death, whichever came first.
Outcome measures
| Measure |
Patients Treated With ABL
n=11027 Participants
Patients who filled ≥ 1 prescription for ABL (TYMLOS) as their index medication during the identification period.
|
Patients Treated With TPTD
n=11027 Participants
Patients who filled ≥ 1 prescription for TPTD (Forteo) as their index medication during the identification period.
|
|---|---|---|
|
Number of Participants With a Composite Endpoint of Nonfatal MI, Nonfatal Stroke, Heart Failure or In-hospital Cardiovascular Death
|
495 Participants
|
471 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: From index date up to 19 monthsPopulation: All patients meeting the study inclusion/exclusion criteria and selected after PS-matching.
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.
Outcome measures
| Measure |
Patients Treated With ABL
n=11027 Participants
Patients who filled ≥ 1 prescription for ABL (TYMLOS) as their index medication during the identification period.
|
Patients Treated With TPTD
n=11027 Participants
Patients who filled ≥ 1 prescription for TPTD (Forteo) as their index medication during the identification period.
|
|---|---|---|
|
Number of Participants With Hip Fracture
|
112 Participants
|
125 Participants
|
Adverse Events
Patients Treated With ABL
Patients Treated With TPTD
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place