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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02186171
Other study ID # 20110174
Secondary ID 2013-005551-32
Status Completed
Phase Phase 3
First received
Last updated
Start date June 16, 2014
Est. completion date April 20, 2016

Study information

Verified date May 2019
Source Amgen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is designed to evaluate if treatment with romosozumab once a month for 12 months compared with placebo is effective in increasing bone mineral density (BMD) at the lumbar spine. Additionally, the study will assess the effect of treatment with romosozumab for 12 months compared with placebo on BMD at the femoral neck and total hip.


Recruitment information / eligibility

Status Completed
Enrollment 245
Est. completion date April 20, 2016
Est. primary completion date February 15, 2016
Accepts healthy volunteers No
Gender Male
Age group 55 Years to 90 Years
Eligibility Inclusion Criteria:

- Must be ambulatory male subjects = 55 years to = 90 years of age

- Must have a BMD T score = -2.50 at the spine or hip, or BMD T score = -1.50 at the spine or hip and a history of fragility nonvertebral fracture or vertebral fracture.

Exclusion Criteria:

- A BMD T score = -3.50 at the hip,

- History of hip fracture

- Severe metabolic bone diseases

- Significant laboratory abnormalities

- Recent treatment with agents affecting bone metabolism

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Romosozumab
Administered by subcutaneous injection once a month.
Drug:
Placebo
Administered by subcutaneous injection once a month.

Locations

Country Name City State
Belgium Research Site Genk
Belgium Research Site Gent
Belgium Research Site Leuven
Belgium Research Site Liège
Colombia Research Site Bogota Cundinamarca
Colombia Research Site Medellin Antioquia
Czechia Research Site Ostrava-Trebovice
Czechia Research Site Plzen
Czechia Research Site Praha 11 - Chodov
Denmark Research Site Aalborg
Denmark Research Site Ballerup
Japan Research Site Bungoono-shi Oita
Japan Research Site Hachioji-shi Tokyo
Japan Research Site Mizunami-shi Gifu
Japan Research Site Shinagawa-ku Tokyo
Japan Research Site Takatsuki-shi Osaka
Japan Research Site Toshima-ku Tokyo
Japan Research Site Yokohama-shi Kanagawa
Mexico Research Site Culiacan Sinaloa
Mexico Research Site Mexicali Baja California Norte
Mexico Research Site Monterrey Nuevo León
Poland Research Site Lodz
Poland Research Site Swidnik
Poland Research Site Warszawa
Poland Research Site Wroclaw
Russian Federation Research Site Moscow
Russian Federation Research Site Saint-Petersburg
Russian Federation Research Site Yaroslavl
Switzerland Research Site Bern
Switzerland Research Site Zurich
Switzerland Research Site Zurich
United States Research Site Albuquerque New Mexico
United States Research Site Bethesda Maryland
United States Research Site Lakewood Colorado

Sponsors (1)

Lead Sponsor Collaborator
Amgen

Countries where clinical trial is conducted

United States,  Belgium,  Colombia,  Czechia,  Denmark,  Japan,  Mexico,  Poland,  Russian Federation,  Switzerland, 

References & Publications (1)

Lewiecki EM, Blicharski T, Goemaere S, Lippuner K, Meisner PD, Miller PD, Miyauchi A, Maddox J, Chen L, Horlait S. A Phase III Randomized Placebo-Controlled Trial to Evaluate Efficacy and Safety of Romosozumab in Men With Osteoporosis. J Clin Endocrinol Metab. 2018 Sep 1;103(9):3183-3193. doi: 10.1210/jc.2017-02163. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Percent Change From Baseline in Lumbar Spine Bone Mineral Density (BMD) at Month 12 Lumbar spine bone mineral density (BMD) was measured by dual x-ray absorptiometry (DXA). DXA scans were analyzed by a central imaging center. Baseline and month 12
Secondary Percent Change From Baseline in BMD at the Total Hip at Month 12 Total hip bone mineral density was measured by dual x-ray absorptiometry (DXA). DXA scans were analyzed by a central imaging center. Baseline and month 12
Secondary Percent Change From Baseline in BMD at the Femoral Neck at Month 12 Femoral neck bone mineral density (BMD) was measured by dual x-ray absorptiometry (DXA). DXA scans were analyzed by a central imaging center. Baseline and month 12
Secondary Percent Change From Baseline in Lumbar Spine BMD at Month 6 Lumbar spine bone mineral density (BMD) was measured by dual x-ray absorptiometry (DXA). DXA scans were analyzed by a central imaging center. Baseline and month 6
Secondary Percent Change From Baseline in BMD at the Total Hip at Month 6 Bone mineral density was measured by dual x-ray absorptiometry (DXA). DXA scans were analyzed by a central imaging center. Baseline and month 6
Secondary Percent Change From Baseline in BMD at the Femoral Neck at Month 6 Bone mineral density (BMD) was measured by dual x-ray absorptiometry (DXA). DXA scans were analyzed by a central imaging center. Baseline and month 6