Preserved supervised synthesis

Teriparatide synthesis · version 1

This URL preserves the exact reviewed public wording and source set for synthesis version 1.

Supervised synthesis

What do selected human studies report about Teriparatide?

Manually reviewed August 19, 2026 · version 1

Browse all Human Evidence Reviews · Open preserved synthesis version 1 →

A bounded review of two randomized fracture trials in postmenopausal women with osteoporosis, including one placebo comparison and one active comparison with risedronate.12

Bottom line from this bounded source set

Both reviewed trials reported fewer new vertebral fractures with teriparatide than with the comparator. The active-comparator trial did not find a statistically significant difference for its nonvertebral fragility-fracture endpoint.12

Reviewed study record

Placebo-controlled fracture trial

Design

A randomized placebo-controlled trial assessed new vertebral and nonvertebral fractures and bone mineral density over a median observation period of 21 months.1

Population

The trial randomized 1,637 postmenopausal women with osteoporosis and prior vertebral fractures.1

Outcomes reported

New vertebral fractures occurred in 14% of the placebo group and 5% and 4% of the two teriparatide groups; nonvertebral fragility fractures occurred in 6% and 3%, respectively.1

Limitations

The population had established postmenopausal osteoporosis with prior vertebral fractures, so the results do not establish effects in people with different baseline risk.1

Reviewed study record

VERO active-comparator fracture trial

Design

A sponsor-funded, double-blind, double-dummy randomized trial compared teriparatide with risedronate over 24 months, with new radiographic vertebral fractures as the primary outcome.2

Population

The trial randomized 1,360 postmenopausal women with severe osteoporosis and qualifying vertebral fractures.2

Outcomes reported

New vertebral fractures were reported in 5.4% of the teriparatide group and 12.0% of the risedronate group. The reported nonvertebral fragility-fracture difference was not statistically significant.2

Limitations

The sponsor-funded results apply to women with severe osteoporosis and existing vertebral-fracture history; the nonvertebral endpoint remained statistically uncertain.2

Reviewed source set

  1. PubMed · 11346808Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis ↗PubMed PMID 11346808 · EFetch XML reviewed 2026-08-19 · payload SHA-256 6e178a71aed55efb345f0b59ad938e7c5c0db5692d911f30c23ae4d66e0627b2
    No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1056/nejm200105103441904. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗
  2. PubMed · 29129436Effects of teriparatide and risedronate on new fractures in post-menopausal women with severe osteoporosis (VERO): a multicentre, double-blind, double-dummy, randomised controlled trial ↗PubMed PMID 29129436 · EFetch XML reviewed 2026-08-19 · payload SHA-256 36f2e43b6083d116716442ec30a08f20413f3bbae83e308678d58c0ec185b2f1
    No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1016/s0140-6736(17)32137-2. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗