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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00619957
Other study ID # 2001092 and 2001092 OL
Secondary ID
Status Completed
Phase Phase 3
First received February 11, 2008
Last updated September 20, 2011
Start date June 2002
Est. completion date May 2007

Study information

Verified date September 2011
Source Warner Chilcott
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Two year study to determine the safety and efficacy of weekly 35 mg Risedronate doses in men with osteoporosis followed by a two year follow-up study.


Recruitment information / eligibility

Status Completed
Enrollment 285
Est. completion date May 2007
Est. primary completion date May 2007
Accepts healthy volunteers No
Gender Male
Age group 30 Years and older
Eligibility Inclusion Criteria:

- Documented osteoporosis of the femoral neck and lumbar spine

Exclusion Criteria:

- BMI greater than or equal to 35

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Placebo tablet
one placebo once a week for two years followed by one 35 mg risedronate once a week for two years
Risedronate
one 35 mg risedronate once a week for two years followed by one 35 mg risedronate once a week for two years

Locations

Country Name City State
Australia Research Facility Concord
Australia Research Facility Heidelburg
Belgium Research Facility Leuven
Czech Republic Research Site Prague
France Research Facility Angers
France Research Site Lyon
Hungary Research Facility Budapest
Hungary Research Site Budapest
Lebanon Research Site Beirut
Netherlands Research Site Rotterdam
Poland Research Site Bialystok
Poland Research Site Warsaw
Poland Research Site Wroclaw
United Kingdom Research Site London
United Kingdom Research Site Newcastle
United Kingdom Research Site Sheffield
United States Research Facility Cincinnati Ohio
United States Research Site Lakewood Colorado
United States Research Site Palm Desert California
United States Research Site Portland Oregon
United States Research Site St. Louis Missouri
United States Research Site Stuart Florida
United States Research Site Wyomissing Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Warner Chilcott Sanofi

Countries where clinical trial is conducted

United States,  Australia,  Belgium,  Czech Republic,  France,  Hungary,  Lebanon,  Netherlands,  Poland,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent Change From Baseline in Lumbar Spine Bone Mineral Density (BMD), 24 Months/Endpoint, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Site will perform at screening to determine if scan should be forwarded to central facility for analysis. Mean of 2 scans performed read by central lab to determine entry qualification. Results standardized (sBMD): Hologic sBMD = 1000 x (BMD x 1.0755), Lunar sBMD = 1000 x (BMD x 0.9522). Baseline to 24 Months/Endpoint Yes
Secondary Percent Change From Baseline in Lumbar Spine BMD, Month 6, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines and forwarded to central laboratory for reading.DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Results standardized (sBMD): Hologic sBMD = 1000 x (BMD x 1.0755), Lunar sBMD = 1000 x (BMD x 0.9522). Baseline to Month 6 Yes
Secondary Percent Change From Baseline in Lumbar Spine BMD, Month 12, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines and forwarded to central laboratory for reading. Results standardized (sBMD): Hologic sBMD = 1000 x (BMD x 1.0755), Lunar sBMD = 1000 x (BMD x 0.9522). Baseline to Month 12 Yes
Secondary Percent Change From Baseline in Lumbar Spine BMD, Month 24, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines and forwarded to central laboratory for reading. Mean of 2 scans performed. Results standardized (sBMD): Hologic sBMD = 1000 x (BMD x 1.0755), Lunar sBMD = 1000 x (BMD x 0.9522). Baseline to Month 24 Yes
Secondary Percent Change From Baseline in Total Proximal Femur BMD, Month 6, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines and forwarded to central laboratory for reading. Results standardized (sBMD): Hologic sBMD = 1000 x (1.008 x BMD + 0.006), Lunar sBMD = 1000 x (0.979 x BMD - 0.031). Baseline to Month 6 Yes
Secondary Percent Change From Baseline in Total Proximal Femur BMD, Month 12, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines and forwarded to central laboratory for reading. Results standardized (sBMD): Hologic sBMD = 1000 x (1.008 x BMD + 0.006), Lunar sBMD = 1000 x (0.979 x BMD - 0.031). Baseline to Month 12 Yes
Secondary Percent Change From Baseline in Total Proximal Femur BMD, Month 24, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Mean of 2 scans performed will be utilized. Results standardized (sBMD): Hologic sBMD = 1000 x (1.008 x BMD + 0.006), Lunar sBMD = 1000 x (0.979 x BMD - 0.031). Baseline to Month 24 Yes
Secondary Percent Change From Baseline in Total Proximal Femur BMD, 24 Months/Endpoint, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Mean of 2 scans performed will be utilized. Results standardized (sBMD): Hologic sBMD = 1000 x (1.008 x BMD + 0.006), Lunar sBMD = 1000 x (0.979 x BMD - 0.031). Baseline to 24 Months/Endpoint Yes
Secondary Percent Change From Baseline in Femoral Neck BMD, Month 6, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Baseline femoral neck values measured on Lunar instruments will be normalized to Hologic reference. Hologic Reference BMD = (0.836 x BMD[lunar]) - 0.008 Baseline to Month 6 Yes
Secondary Percent Change From Baseline in Femoral Neck BMD, Month 12, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Baseline femoral neck values measured on Lunar instruments will be normalized to Hologic reference. Hologic reference BMD = (0.836 x BMD[lunar]) - 0.008 Baseline to Month 12 Yes
Secondary Percent Change From Baseline in Femoral Neck BMD, Month 24, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Mean of 2 scans performed will be utilized. Baseline femoral neck values measured on Lunar instruments will be normalized to Hologic reference. Hologic reference BMD = (0.836 x BMD[lunar]) - 0.008 Baseline to Month 24 Yes
Secondary Percent Change From Baseline in Femoral Neck BMD, 24 Months/Endpoint, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Mean of 2 scans performed will be utilized. Baseline femoral neck values measured on Lunar instruments will be normalized to Hologic reference. Hologic reference BMD = (0.836 x BMD[lunar]) - 0.008 Baseline to 24 Months/Endpoint Yes
Secondary Percent Change From Baseline in Femoral Trochanter BMD, Month 6, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Baseline to Month 6 Yes
Secondary Percent Change From Baseline in Femoral Trochanter BMD, Month 12, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Baseline to Month 12 Yes
Secondary Percent Change From Baseline in Femoral Trochanter BMD, Month 24, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Baseline to Month 24 Yes
Secondary Percent Change From Baseline in Femoral Trochanter BMD, 24 Months/Endpoint, ITT Population. DXA (dual energy x-ray absorptiometry) assayed on Lunar or Hologic machines. Scans will be forwarded to central facility for analysis. Baseline to 24 Months/Endpoint Yes
Secondary Percent Change From Baseline in CTx (Type I Collagen C-telopeptide), Month 3, ITT Population. Baseline to Month 3 Yes
Secondary Percent Change From Baseline in CTx, Month 6, ITT Population. Baseline to Month 6 Yes
Secondary Percent Change From Baseline in CTx, Month 12, ITT Population. Baseline to Month 12 Yes
Secondary Percent Change From Baseline in CTx, Month 24, ITT Population. Baseline to Month 24 Yes
Secondary Percent Change From Baseline in CTx, 24 Months/Endpoint, ITT Population. Baseline to 24 Months/Endpoint Yes
Secondary Percent Change From Baseline in NTx/Cr (Type I Collagen N-telopeptide/Creatinine), Month 3, ITT Population. Baseline to Month 3 Yes
Secondary Percent Change From Baseline in NTx/Cr, Month 6, ITT Population. Baseline to Month 6 Yes
Secondary Percent Change From Baseline in NTx/Cr, Month 12, ITT Population. Baseline to Month 12 Yes
Secondary Percent Change From Baseline in NTx/Cr, Month 24, ITT Population. Baseline to Month 24 Yes
Secondary Percent Change From Baseline in NTx/Cr, 24 Months/Endpoint, ITT Population. Baseline to 24 Months/Endpoint Yes
Secondary Percent Change From Baseline in BAP (Bone-specific Alkaline Phosphatase), Month 3, ITT Population. Baseline to Month 3 Yes
Secondary Percent Change From Baseline in BAP, Month 6, ITT Population. Baseline to Month 6 Yes
Secondary Percent Change From Baseline in BAP, Month 12, ITT Population. Baseline to Month 12 Yes
Secondary Percent Change From Baseline in BAP, Month 24, ITT Population. Baseline to Month 24 Yes
Secondary Percent Change From Baseline in BAP, 24 Months/Endpoint, ITT Population. Baseline to 24 Months/Endpoint Yes
Secondary Change From Baseline in Body Height, Month 12, ITT Population. Baseline to Month 12 Yes
Secondary Change From Baseline in Body Height, Month 24, ITT Population. Baseline to Month 24 Yes
Secondary Change From Baseline in Body Height, 24 Months/Endpoint, ITT Population. Baseline to 24 Months/Endpoint Yes
Secondary Percent of Responders Lumbar Spine BMD, Month 24, ITT Population responder = positive change (>0) in lumbar spine BMD from Baseline to Month 24 Baseline to Month 24 No
Secondary Cumulative Incidence of Fractures, 12 Months, ITT Population Kaplan-Meier Cumulative Incidence, fractures / 100 patients / year Baseline to Month 12 No
Secondary Cumulative Incidence of Fractures, 24 Months, ITT Population Kaplan-Meier Cumulative Incidence, fractures / 100 patients / 2 years Baseline to Month 24 No