A Prostate Cancer Study in Men Undergoing Androgen Deprivation Therapy

Not Applicable

Completed

• Conditions: Prostate Cancer

• Registration Number: NCT00087659
• Lead Sponsor: Novartis Pharmaceuticals

Brief Summary

This study is being conducted to compare the effect of an investigational drug versus placebo on bone loss in men with prostate cancer who are receiving Androgen Deprivation Therapy (ADT). The study drug or placebo will be administered every three months of four treatments in one year.

In order to participate, male patients 18 years and older must be consecutive veterans from participating Veterans Administration Medical Centers.

Detailed Description

Not available

Study Timeline

• Study Start: 2003-12
• Study First Submitted: 2004-07-12
• Study First Submitted QC: 2004-07-13
• Study First Posted: 2004-07-14
• Study Completion: 2007-05
• Status Verified: 2009-11
• Last Update Submitted: 2009-11-20
• Last Update Posted: 2009-11-23

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

• Signed informed consent
• Age > 18 years
• Histologically confirmed diagnosis of carcinoma of the prostate
• No distant metastases at the start of ADT and continuously low PSA (<2.0) on continuous ADT (stage Tany Nany MO).
• Patients initiating or receiving ADT with a LHRH agonist (with or without an antiandrogen) and with the intended duration of ADT of at least 12 months at the time of randomization. Patients undergoing bilateral orchiectomy or with history of this procedure are also eligible.
• Patient with a baseline BMD T-score at or above -2.0 standard deviations in the lumbar spine (L2-L4) and the total hip are eligible
• Life expectancy of at least 12 months
• Zubrod performance status of 0, 1, or 2

Exclusion Criteria

• Patients who received any prior bisphosphonate therapy in the past 6 months

• Metabolic bone disease including Paget's disease or hyperparathyroidism

• Radiographic evidence of bone metastases

• Patients who have received prior treatment with systemic corticosteroids within the past 12 months (short term corticosteroid therapy, e.g. to prevent/treat chemotherapy-induced nausea/vomiting or for acute illness like asthma exacerbation, is acceptable)

• Patients with prior exposure to anabolic steroids or growth hormone within the past 6 months

• Current treatment with estrogen or complementary medicines known to contain estrogens

• Patients with clinical or radiological evidence of existing fracture in the lumbar spine and/or total hip

• Patients with a history of fracture with low-intensity or no associated trauma

• Patients with any prior treatment for osteoporosis

• Patients with previous or concomitant malignancy within the past 5 years except adequately treated basal or squamous cell carcinoma of the skin, and colonic polyps with non-invasive malignancy which have been removed

• Patients with nonmalignant conditions which would confound the evaluation of the primary endpoint, impair tolerance of therapy, or prevent compliance to the protocol, including:

  • uncontrolled infections
  • uncontrolled type 2 diabetes mellitus
  • diseases with influence on bone metabolism, such as Paget's disease or uncontrolled thyroid or parathyroid dysfunction
  • cardiovascular, renal, hepatic, pulmonary and neurologic/psychiatric diseases which would prevent prolonged follow-up

• History of surgery at the lumbosacral spine, with or without implantable devices, bilateral hip replacement or bilateral hip surgery with implantation of an appliance

• Patients treated with systemic investigational drugs(s) and /or device(s) within the past 30 days

• Patients with abnormal renal function as evidenced by either a serum creatinine greater than 3 mg/dL or by a calculated creatinine clearance of 60 ml/minute or less

• Corrected (adjusted for serum albumin) serum calcium concentration < 8.0 mg/dl (2.00 mmol/L)

• Subjects who, in the opinion of the investigator, are unlikely to cooperate fully during the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Percent change in bone mineral density of the lumbar spine (L2-L4) at 6 and 12 months.

Secondary Outcome Measures

Name	Time	Method
Percent change in bone mineral density of the total hip (including femoral neck, trachanteric region, and Ward's triangle) following one year of therapy.

Trial Locations

Locations (15)

Veterans Affairs Medical Center; 🇺🇸 Augusta, Georgia, United States

WJB Dorn Veteran Affairs Medical Center; 🇺🇸 Columbia, South Carolina, United States

West Sde Vamc; 🇺🇸 Chicago, Illinois, United States

Hines VA Medical Center; 🇺🇸 Hines, Illinois, United States

West Roxbury VAMC; 🇺🇸 West Roxbury, Massachusetts, United States

Atlanta VA Medical Center; 🇺🇸 Decatur, Georgia, United States

Kansas City VAMC; 🇺🇸 Kansas City, Missouri, United States

John D. Dingell VA Medical Center; 🇺🇸 Detroit, Michigan, United States

Washington VA Medical Center; 🇺🇸 Washington, District of Columbia, United States

VA Medical Center - Long Beach; 🇺🇸 Long Beach, California, United States

Department of Veterans Affairs; 🇺🇸 East Orange, New Jersey, United States

VAWNY, Buffalo; 🇺🇸 Buffalo, New York, United States

Louisville VAMC; 🇺🇸 Louisville, Kentucky, United States

Portland/Vancouver; 🇺🇸 Portland, Oregon, United States

Tucson VA Medical Center; 🇺🇸 Tucson, Arizona, United States