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Phase 3 N=327 Randomized Quadruple-blind Treatment

A Study to Test the Efficacy, Safety and Tolerability of Romosozumab Treatment in Postmenopausal Chinese Women With Osteoporosis

Osteoporosis

Enrolled (actual)
327
Serious AEs
7.3%
Results posted
Dec 2024
Primary outcome: Primary: Percent Change From Baseline in Bone Mineral Density (BMD) at the Lumbar Spine to the End of Double-Blind Period — 0.44; 9.81 percent change — p=<0.001

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Romosozumab (Drug); Placebo (Drug)
Age
Adult, Older Adult · 55+ yrs
Sex
Female
Sponsor
UCB Biopharma SRL
Primary completion
Nov 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Percent Change From Baseline in Bone Mineral Density (BMD) at the Lumbar Spine to the End of Double-Blind Period
0.44; 9.81 <0.001 sig
PRIMARY
Percentage of Participants With Treatment-emergent Adverse Events (TEAEs) During the Double-Blind Period
70.6; 72.9
PRIMARY
Percentage of Participants With Treatment-emergent Adverse Events for Romosozumab During Overall Period
80.6; 88.1
SECONDARY
Percent Change From Baseline in Bone Mineral Density at the Total Hip to the End of Double-Blind Period
0.07; 2.93 <0.001 sig
SECONDARY
Percent Change From Baseline in Bone Mineral Density at the Femoral Neck to the End of the Double-Blind Period
-0.15; 3.33 <0.001 sig
SECONDARY
Percent Change From Baseline in Bone Mineral Density at the Lumbar Spine at Month 12
8.80; 13.04
SECONDARY
Percent Change From Baseline in Bone Mineral Density at the Total Hip at Month 12
1.83; 4.22
SECONDARY
Percent Change From Baseline in Bone Mineral Density at the Femoral Neck at Month 12
1.87; 4.66

Summary

The purpose of the study is to evaluate the effect of treatment with romosozumab for 6 months compared with placebo on the percent changes in bone mineral density (BMD) at the lumbar spine, at the total hip and femoral neck in postmenopausal Chinese women with osteoporosis.

Eligibility Criteria

Inclusion Criteria

  • Subject is considered reliable and capable of adhering to the protocol, visit schedule, and medication intake according to the judgment of the investigator
  • Subject is an ambulatory postmenopausal Chinese women, 55 to 90 years of age (inclusive) at the time of Screening. Postmenopause is defined as no spontaneous vaginal bleeding or spotting for 12 or more consecutive months prior to Screening
  • Subject has a bone mineral density (BMD) T-score ≤-2.50 at the lumbar spine, total hip, or femoral neck, as assessed by the central imaging vendor at the time of Screening based on DXA scans, and using data for Caucasian women from the National Health and Nutritional Examination Survey (NHANES, 1998)
  • Subject must have at least 1 of following independent risk factors for fracture:
  • History of fragility fracture (except hip fracture, a severe vertebral fracture or more than 2 moderate vertebral fractures)
  • Parental history of hip fracture
  • Low body weight (body mass index ≤19kg/m2)
  • Elderly (age ≥ 65 years)
  • Current smoker
  • Subject has at least 2 vertebrae in the L1 to L4 region and at least 1 hip that are evaluable by dual-energy x-ray absorptiometry (DXA), as assessed by the central imaging vendor

Exclusion Criteria

  • Subject has a BMD T-score of ≤-3.50 at the total hip or femoral neck, as assessed by the central imaging vendor at the time of Screening based on DXA scans, and using data for Caucasian women from NHANES 1998
  • Subject has a known history of hip fracture
  • Subject has any severe (SQ3) or more than 2 moderate (SQ2) vertebral fractures, as assessed by the central imaging vendor based on the lateral spine x-ray at Screening
  • Subject has a history of myocardial infarction (MI)
  • Subject has a history of stroke
  • Subject has a vitamin D insufficiency, defined as 25 (OH) vitamin D levels 10
  • Current, uncontrolled hyperparathyroidism or history of hypoparathyroidism. Uncontrolled hyperparathyroidism is defined as PTH outside the normal range in subjects with concurrent hypercalcemia or PTH values >20 % above upper limit of normal (ULN) in normocalcemic subjects
  • Current hypercalcemia or hypocalcemia, defined as albumin-adjusted serum calcium outside the normal range, as assessed by the central laboratory at the time of Screening. Albumin-adjusted serum calcium levels may be retested once in case of an elevated albumin-adjusted serum calcium level within 1.1xULN of the laboratory's reference ranges
  • Subject has ≥3xULN of any of the following: alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), or >ULN total bilirubin (≥1.5xULN total bilirubin if known Gilbert's syndrome). If subject has elevations only in total bilirubin that are >ULN and <1.5xULN, fractionate bilirubin to identify possible undiagnosed Gilbert's syndrome (ie, direct bilirubin <35 %)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05067335). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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