Status:
COMPLETED
Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Denosumab (AMG 162) in Japanese Postmenopausal Women
Lead Sponsor:
Amgen
Conditions:
Osteoporosis
Phase:
PHASE1
Brief Summary
The primary objective was to evaluate the safety and tolerability of denosumab (AMG 162) after a single subcutaneous administration in Japanese postmenopausal women.
Eligibility Criteria
Inclusion
- ambulatory women between the ages of 40 and 64 years, inclusive
- postmenopausal, defined as amenorrheic for at least 24 months
- clinically acceptable physical exam
- clinical laboratory tests (complete blood count \[CBC\], blood chemistries, urinalysis) within normal limits or clinically acceptable to the investigator/sponsor at the time of screening with the exception of aspartate transaminase (AST) and alkaline phosphatase (ALT), which must be \< 1.25 times the upper limit of normal, or gamma-glutamyl transpeptidase (GGT), which must be \< 1.5 times the upper limit of normal
- normal or clinically acceptable electrocardiogram (ECG) (12-lead reporting ventricular rate and PR, QRS, QT, and QTc intervals)
- body mass index between 17 and 27
- willing to sign an approved informed consent form before any study-specific assessments and oral consultations are performed
Exclusion
- administration of medications within 6 months before investigational product administration that are known to effect bone metabolism, including but not limited to the following: calcitonin, parathyroid hormone (or any derivative), supplemental vitamin D (\> 1000 IU/day), glucocorticosteroids (inhaled or topical corticosteroids administered more than 2 weeks before the date of informed consent were allowed), anabolic steroids, calcitriol and available analogues, diuretics
- administration of the following medications within 12 months before study drug administration: bisphosphonates, fluoride for osteoporosis
- diagnosed with any condition that affects bone metabolism
- greatly differing levels of physical activity compared with the 6 months before investigational product administration or constant levels of intense physical activities
- routine alcohol intake of ≥ 2 drinks/day, on average, within 6 months of investigational product administration
- known sensitivity to any drugs
- positive test results for hepatitis B surface antigen, hepatitis C virus, human immunodeficiency virus antigen/antibody, syphilis
- receiving or received any investigational drug (or was currently using an investigational device) within 4 months before receiving investigational product
- donated any amount of blood within 16 weeks, or over 400 mL (Note: not 400 mL but 200 mL, for the subjects who were to be enrolled into cohorts 4 or 5) within 1 year of the start day of screening
- subject had previously entered this study
- any other condition that might have reduced the chance of obtaining data (eg, known poor compliance) required by the protocol or that might have compromised the ability to give truly informed consent
Key Trial Info
Start Date :
September 30 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 24 2004
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT03822078
Start Date
September 30 2003
End Date
December 24 2004
Last Update
July 24 2019
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