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

Primary Purpose

Renal Insufficiency, Chronic

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
paricalcitol
Sponsored by
Abbott
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Insufficiency, Chronic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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 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

Sites / Locations

  • UCI Medical Center
  • Western Nephrology
  • Outcomes Research International, Inc.
  • Nephrology Association of South Miami
  • Tampa Bay Nephrology Associates
  • Northwestern University Medical School
  • University of Missouri Health Sciences Center
  • Arms, Dodge, Robinson, Wilber and Crouch
  • Washington University School of Medicine
  • NEA Research
  • North Shore University Hospital
  • Mount Sinai School of Medicine
  • Wake Nephrology Associates, PA
  • Kidney and Hypertension Center
  • Dorn VA Hospital
  • Dallas Nephrology Associates
  • The Vancouver Clinic, Inc., P.S.
  • Jagiellonian University

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Full Information

First Posted
October 31, 2002
Last Updated
August 10, 2006
Sponsor
Abbott
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1. Study Identification

Unique Protocol Identification Number
NCT00048438
Brief Title
Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic Kidney Disease Subjects (Three Times Weekly)
Official Title
Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic Kidney Disease Subjects (Three Times Weekly)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2006
Overall Recruitment Status
Completed
Study Start Date
February 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Abbott

4. Oversight

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Insufficiency, Chronic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
68 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
paricalcitol
Primary Outcome Measure Information:
Title
The efficacy endpoint is achievement of two consecutive > or = 30% decreases from baseline iPTH levels.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laura Williams, M.D.
Organizational Affiliation
Abbott
Official's Role
Study Director
Facility Information:
Facility Name
UCI Medical Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
Western Nephrology
City
Thornton
State/Province
Colorado
ZIP/Postal Code
80260
Country
United States
Facility Name
Outcomes Research International, Inc.
City
Hudson
State/Province
Florida
ZIP/Postal Code
34667
Country
United States
Facility Name
Nephrology Association of South Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33173
Country
United States
Facility Name
Tampa Bay Nephrology Associates
City
Tampa
State/Province
Florida
ZIP/Postal Code
33603
Country
United States
Facility Name
Northwestern University Medical School
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
University of Missouri Health Sciences Center
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65212
Country
United States
Facility Name
Arms, Dodge, Robinson, Wilber and Crouch
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64111
Country
United States
Facility Name
Washington University School of Medicine
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
NEA Research
City
Las Vegas
State/Province
Nevada
ZIP/Postal Code
89102
Country
United States
Facility Name
North Shore University Hospital
City
Great Neck
State/Province
New York
ZIP/Postal Code
11021
Country
United States
Facility Name
Mount Sinai School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
Wake Nephrology Associates, PA
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27609
Country
United States
Facility Name
Kidney and Hypertension Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45220
Country
United States
Facility Name
Dorn VA Hospital
City
Columbia
State/Province
South Carolina
ZIP/Postal Code
29209
Country
United States
Facility Name
Dallas Nephrology Associates
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States
Facility Name
The Vancouver Clinic, Inc., P.S.
City
Vancouver
State/Province
Washington
ZIP/Postal Code
98644
Country
United States
Facility Name
Jagiellonian University
City
Cracow
Country
Poland

12. IPD Sharing Statement

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

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