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NCT00890981COMPLETEDanonymous

A HR-pQCT Study in Postmenopausal Women Previously Treated With Denosumab

Sponsor

Source record

Amgen

Phase

Source record

PHASE3

Modality

AI-normalized

monoclonal antibody

Target

AI-normalized

high-resolution peripheral quantitative computed tomography (HR-pQCT), Dual energy X-ray absorptiometry (DXA), Denosumab, Placebo

Indication / condition

AI-normalized

Low Bone Mass

Intervention

Source record

high-resolution peripheral quantitative computed tomography (HR-pQCT), Dual energy X-ray absorptiometry (DXA), Denosumab, Placebo

Source & freshness

Source record

NCT ID

NCT00890981

Original source

ClinicalTrials.gov

Source last updated

Apr 02, 2014

Ingested at

May 21, 2026

Internal sync

May 23, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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View original source fields

NCT ID

NCT00890981

Title

A HR-pQCT Study in Postmenopausal Women Previously Treated With Denosumab

Sponsor

Amgen

Status

COMPLETED

Phase

PHASE3

Condition raw

Low Bone Mass, Low Bone Mineral Density, Osteoporosis, Postmenopausal Osteoporosis

Condition normalized

Low Bone Mass, Low Bone Mineral Density, Osteoporosis, Postmenopausal Osteoporosis

Modality raw

monoclonal antibody

Modality normalized

monoclonal antibody

Target raw

high-resolution peripheral quantitative computed tomography (HR-pQCT), Dual energy X-ray absorptiometry (DXA), Denosumab, Placebo

Target normalized

high-resolution peripheral quantitative computed tomography (HR-pQCT), Dual energy X-ray absorptiometry (DXA), Denosumab, Placebo

Interventions

high-resolution peripheral quantitative computed tomography (HR-pQCT), Dual energy X-ray absorptiometry (DXA), Denosumab, Placebo

Public preview

Source record

To evaluate the combined effect of denosumab treatment and discontinuation on cortical thickness at the distal radius by High Resolution-Peripheral Quantitative Computed Tomography (HR-pQCT). Participants randomized to either denosumab or placebo in the 20050179 (NCT00293813) study who completed that study (ie, attended an end of study visit) can be included in this study. At least 12 months should have elapsed since the patient's 20050179 end of study visit.

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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