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Study · Randomized controlled trial · 2017

2 results

Greater Gains in Spine and Hip Strength for Romosozumab Compared With Teriparatide in Postmenopausal Women With Low Bone Mass.

Keaveny TM, Crittenden DB, Bolognese MA, Genant HK, Engelke K, Oliveri B, Brown JP, Langdahl BL, Yan C, Grauer A, Libanati C

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research26 Jun 2017Cited by 74 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study2

2 results from studies that gave the peptide. 2 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In postmenopausal women with low bone mass, estimated vertebral strength (finite element analysis of CT scans) increased by 18.5% with teriparatide versus 27.3% with romosozumab at month 12.

    In plain wordsIn postmenopausal women with low bone mass, estimated spine strength rose less with teriparatide than with romosozumab after 12 months.

    Outcome
    DecreaseVertebral strength
    Study

    n: not reported in source

    Comparator
    Romosozumab
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    20 μg daily · 12 monthsAs given in this study (human).

    Measurements

    Vertebral strength change
    18.5%
    teriparatide
    Vertebral strength change
    27.3%
    romosozumab

    Source sentences

    Summary
    We found that, at month 12, vertebral strength increased more for romosozumab compared with both teriparatide (27.3% versus 18.5%; p = 0.005) and placebo (27.3% versus -3.9%; p < 0.0001);
    2 context sentences
    Summary · context
    In a substudy of that trial, which included placebo and teriparatide arms, here we investigated whether those observed increases in BMD also resulted in improvements in estimated strength, as assessed by finite element analysis.
    Summary · context
    Participants received blinded romosozumab s.c. (210 mg monthly) or placebo, or open-label teriparatide (20 μg daily) for 12 months.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In postmenopausal women with low bone mass, estimated femoral strength (finite element analysis of CT scans) changed by -0.7% with teriparatide versus an increase of 3.6% with romosozumab at month 12.

    In plain wordsIn postmenopausal women with low bone mass, estimated hip strength changed less favorably with teriparatide than with romosozumab after 12 months.

    Outcome
    DecreaseFemoral strength
    Study

    n: not reported in source

    Comparator
    Romosozumab
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    20 μg daily · 12 monthsAs given in this study (human).

    Measurements

    Femoral strength change
    −0.7%
    teriparatide
    Femoral strength change
    3.6%
    romosozumab

    Source sentences

    Summary
    changes in femoral strength for romosozumab showed similar but smaller changes, increasing more with romosozumab versus teriparatide (3.6% versus -0.7%; p = 0.027), and trending higher versus placebo (3.6% versus -0.1%; p = 0.059).
    2 context sentences
    Summary · context
    In a substudy of that trial, which included placebo and teriparatide arms, here we investigated whether those observed increases in BMD also resulted in improvements in estimated strength, as assessed by finite element analysis.
    Summary · context
    Participants received blinded romosozumab s.c. (210 mg monthly) or placebo, or open-label teriparatide (20 μg daily) for 12 months.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Registered trials1

Trials this study reports on, or that list this study as a reference. Registry data from ClinicalTrials.gov.

1 trial · 1 completed · 1 with posted results · source ClinicalTrials.gov (opens in a new tab)

CompletedPhase 2Results postedNCT00896532

Romosozumab (AMG 785) in Postmenopausal Women With Low Bone Mineral Density

Amgenn = 4193 Jun 2009 to 18 Feb 2016

Low Bone Mineral Density · Postmenopausal Osteoporosis

Trial pageClinicalTrials.govUpdated 22 Sept 2022

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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