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CompletedNCT00048438Updated Aug 15, 2006

Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic Kidney Disease Subjects (Three Times Weekly)

A Phase 3 interventional study of paricalcitol in Renal Insufficiency, Chronic, sponsored by Abbott. Completed at 18 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2006-08-15.

Sponsored by Abbott · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
68
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The objective of this study is to determine whether paricalcitol is safe and effective compared to placebo in reducing elevated serum PTH levels in patients with chronic kidney disease.

02

Conditions studied

03

In context

Kidney Diseases

3,840 studies on the registry are indexed under Kidney Diseases; 500 are open to participants now.

This study's enrollment of 68 is close to the median of 70 across 2,640 interventional studies indexed under Kidney Diseases.

Browse Kidney Diseases studies →

Lead sponsor

Abbott is the lead sponsor of 350 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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 mos. 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
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
68 participants

Interventions

  • Drugparicalcitol
06

What researchers measure

Primary outcomes

  1. The efficacy endpoint is achievement of two consecutive > or = 30% decreases from baseline iPTH levels.

07

Study locations

18 sites
  • UCI Medical Center
    Orange, California 92868, United States
  • Western Nephrology
    Thornton, Colorado 80260, United States
  • Outcomes Research International, Inc.
    Hudson, Florida 34667, United States
  • Nephrology Association of South Miami
    Miami, Florida 33173, United States
  • Tampa Bay Nephrology Associates
    Tampa, Florida 33603, United States
  • Northwestern University Medical School
    Chicago, Illinois 60611, United States
  • University of Missouri Health Sciences Center
    Columbia, Missouri 65212, United States
  • Arms, Dodge, Robinson, Wilber and Crouch
    Kansas City, Missouri 64111, United States
  • Washington University School of Medicine
    St. Louis, Missouri 63110, United States
  • NEA Research
    Las Vegas, Nevada 89102, United States
  • North Shore University Hospital
    Great Neck, New York 11021, United States
  • Mount Sinai School of Medicine
    New York, New York 10029, United States
  • Wake Nephrology Associates, PA
    Raleigh, North Carolina 27609, United States
  • Kidney and Hypertension Center
    Cincinnati, Ohio 45220, United States
  • Dorn VA Hospital
    Columbia, South Carolina 29209, United States
  • Dallas Nephrology Associates
    Dallas, Texas 75235, United States
  • The Vancouver Clinic, Inc., P.S.
    Vancouver, Washington 98644, United States
  • Jagiellonian University
    Cracow, Poland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 15, 2006, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00048438
Lead sponsor
Abbott
First posted
Nov 4, 2002
Start date
Feb 2002
Last update
Aug 15, 2006

Study contacts

Laura Williams, M.D.
study director · Abbott
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2006. You cannot join it, but the record below documents what was studied.

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