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NCT03735537COMPLETEDanonymous

Treatment of Osteogenesis Imperfecta With Parathyroid Hormone and Zoledronic Acid

Sponsor

Source record

University of Edinburgh

Phase

Source record

PHASE4

Modality

AI-normalized

small molecule

Target

AI-normalized

Teriparatide Pen Injector, Zoledronic Acid

Indication / condition

AI-normalized

Osteogenesis Imperfecta

Intervention

Source record

Teriparatide Pen Injector, Zoledronic Acid

Source & freshness

Source record

NCT ID

NCT03735537

Original source

ClinicalTrials.gov

Source last updated

Sep 17, 2025

Ingested at

Jun 11, 2026

Internal sync

Jun 11, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT03735537

Title

Treatment of Osteogenesis Imperfecta With Parathyroid Hormone and Zoledronic Acid

Sponsor

University of Edinburgh

Status

COMPLETED

Phase

PHASE4

Condition raw

Osteogenesis Imperfecta

Condition normalized

Osteogenesis Imperfecta

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Teriparatide Pen Injector, Zoledronic Acid

Target normalized

Teriparatide Pen Injector, Zoledronic Acid

Interventions

Teriparatide Pen Injector, Zoledronic Acid

Public preview

Source record

Osteogenesis imperfecta (OI) is an inherited skeletal disorder characterised by increased risk of fragility fractures. Bisphosphonates are frequently prescribed for adult patients with OI with the aim of preventing fractures but the evidence base for efficacy is poor. Recent evidence suggests that the bone anabolic agent teriparatide (TPTD) increases bone mineral density (BMD) and may have the potential to prevent fractures in OI.

The purpose of the TOPaZ Trial is to investigate if a a two-year course of teriparatide (TPTD) followed by antiresorptive therapy with a single infusion of zoledronic acid (ZA) in adults with OI reduces the proportion of patients who experience a fracture as compared with standard care

Adult patients with a clinical diagnosis of OI who are willing and able to give informed consent and who do not have contraindications to the study medications will be recruited from participating sites. Participants will be randomised 1:1 to receive either standard care for the duration of the trial or TPTD for 24 months followed by a single infusion of ZA, or another antiresorptive agent in the event that ZA is contraindicated.

Participants will attend recruiting centres for a Baseline/Screening visit, at 12 months, 24 months and at the end of the trial for formal study visits with telephone calls every 6 months from a site research nurse. Participants randomised to TPTD will also attend recruiting centre at regular intervals during the 24 month treatment period to collect new supplies of TPTD.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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