Volunteers for Kidney Study
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Study Details
This study is to determine how the investigational drug is absorbed, broken down, and removed from the body in volunteers with kidney impairment on hemodialysis when compared to volunteers with a normal level of kidney function. Information regarding safety and side effects that may occur will also be collected. This study is for research purposes only and is not intended to treat your kidney disease.
Method of Administration: Single oral dose of study drug on 2 separate occasions
Study Period
• 5 days and 4 nights in our research facility, on two separate occasions
• 1 follow-up visit
Compensation
- Qualified participants will be compensated up to $3,225 for time and travel related expenses
- Qualified participants will receive study medication, study related physical exams and laboratory tests
Eligibility Criteria
• 18 to 75 years old
• Women that are postmenopausal or have had a hysterectomy or men who’ve had a vasectomy
• Must have kidney impairment or disease and receiving hemodialysis treatment 3 times per week
• May be seeing a nephrologist, have reduced kidney function, or low creatinine clearance and taking medicine such as:
• Procrit®, Epogen®, or Aranesp® for low blood count
• PhosLo for high blood phosphorus
Research Location:
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