Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic Kidney Disease Subjects (Daily Dosing)
Launched by ABBOTT · Nov 1, 2002
Trial Information
Current as of September 11, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Under care of physician at least 2 months (for CKD)
- • Not on active Vitamin D therapy for at least 4 weeks prior
- * If female:
- • Not of childbearing potential, OR,
- • Practicing birth control
- • Not breastfeeding
- • If taking phosphate binders, on a stable regimen at least 4 weeks prior
- * For entry into Pretreatment Phase:
- • iPTH at least 120 pg/mL
- • GFR of 15-60 mL/min and no dialysis expected for at least 6 months
- * For entry into Treatment Phase:
- • Average of 2 consecutive iPTH values of at least 150 pg/mL, taken at least 1 day apart (all values not less than 120 pg/mL_
- • 2 consecutive corrected serum calcium levels between 8.0-10.0 mg/dL
- • 2 consecutive serum phosphorus levels of not more than 5.2 mg/mL
- Exclusion Criteria:
- • History of allergic reaction or sensitivity to similar drugs
- • Acute Renal Failure within 12 weeks of study
- • Chronic gastrointestinal disease
- • Spot urine result demonstrating a urine-calcium-to-urine creatinine ratio of greater than 0,2, or a history of renal stones
- • Taken aluminum-containing phosphate binders within last 12 weeks, or requires such medication for more than 3 weeks during study
- • Current malignancy, or clinically significant liver disease
- • Active granulomatous disease (TB, sarcoidosis, etc.)
- • History of drug or alcohol abuse within 6 months prior
- • Evidence of poor compliance with diet or medication
- • Received any investigational drug or participated in any device trial within 30 days prior
- • Taking maintenance calcitonin, bisphosphonates, or drugs that may affect calcium or bone metabolism (other than females on stable estrogen and/or progestin therapy)
- • On glucocorticoids for a period of more than 14 days within the last 6 months
- • HIV positive
About Abbott
Abbott is a global healthcare company dedicated to improving lives through innovative medical technologies, diagnostics, nutrition, and branded generic pharmaceuticals. With a commitment to advancing health and wellness, Abbott conducts clinical trials to evaluate the safety and efficacy of its diverse portfolio of products, which span multiple therapeutic areas, including cardiovascular, diabetes care, and neurology. The company employs rigorous research methodologies and collaborates with healthcare professionals and institutions worldwide to ensure the highest standards of clinical integrity and patient safety. Abbott's mission is to deliver impactful solutions that enhance patient outcomes and contribute to the advancement of global healthcare.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Charleston, South Carolina, United States
Charleston, South Carolina, United States
Philadelphia, Pennsylvania, United States
Brooklyn, New York, United States
Arden Hills, Minnesota, United States
Buffalo, New York, United States
Tacoma, Washington, United States
Los Angeles, California, United States
Riverside, California, United States
Simi Valley, California, United States
Denver, Colorado, United States
Denver, Colorado, United States
Des Moines, Iowa, United States
Sioux Falls, South Dakota, United States
Nashville, Tennessee, United States
San Antonio, Texas, United States
Norfolk, Virginia, United States
Bialymstoku, Poland
Krakow, Poland
Patients applied
Trial Officials
Laura Williams, M.D.
Study Director
Abbott
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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