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Search / Trial NCT00048516

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.

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

0 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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