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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

  • Tucson Therapeutic Research Institute, Inc.
  • California Institute of Renal Research
  • Nephrology Educational Services and Research, Inc.
  • Phoenix Internal Medicine Associates
  • University of Florida
  • Miami Kidney Group
  • ICSL Clinical Studies
  • Genesis Clinical Research Corporation
  • Evanston Northwestern Healthcare
  • Medisphere Medical Research Center
  • Ochsner Clinic Chronic Dialysis
  • Biolab Research, LLC
  • The Rogosin Institute
  • Dialysis Clinic, Inc.
  • Kidney Associates
  • Texas Tech University Health Science Center
  • University of Texas Health Science Center
  • Wojskowy Instytut Medyczny

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
July 31, 2006
Sponsor
Abbott
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1. Study Identification

Unique Protocol Identification Number
NCT00048451
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
July 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
Tucson Therapeutic Research Institute, Inc.
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85712
Country
United States
City
Pasadena
State/Province
California
ZIP/Postal Code
91105
Country
United States
Facility Name
California Institute of Renal Research
City
San Diego
State/Province
California
ZIP/Postal Code
92120
Country
United States
Facility Name
Nephrology Educational Services and Research, Inc.
City
Tarzana
State/Province
California
ZIP/Postal Code
91356
Country
United States
Facility Name
Phoenix Internal Medicine Associates
City
Waterbury
State/Province
Connecticut
ZIP/Postal Code
06708
Country
United States
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610
Country
United States
Facility Name
Miami Kidney Group
City
Miami
State/Province
Florida
ZIP/Postal Code
33143
Country
United States
Facility Name
ICSL Clinical Studies
City
Sarasota
State/Province
Florida
ZIP/Postal Code
34232
Country
United States
Facility Name
Genesis Clinical Research Corporation
City
Tampa
State/Province
Florida
ZIP/Postal Code
33614
Country
United States
Facility Name
Evanston Northwestern Healthcare
City
Evanston
State/Province
Illinois
ZIP/Postal Code
60201
Country
United States
Facility Name
Medisphere Medical Research Center
City
Evansville
State/Province
Indiana
ZIP/Postal Code
47714
Country
United States
Facility Name
Ochsner Clinic Chronic Dialysis
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States
Facility Name
Biolab Research, LLC
City
Rockville
State/Province
Maryland
ZIP/Postal Code
20852
Country
United States
Facility Name
The Rogosin Institute
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Dialysis Clinic, Inc.
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45206
Country
United States
Facility Name
Kidney Associates
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Texas Tech University Health Science Center
City
Lubbock
State/Province
Texas
ZIP/Postal Code
79430
Country
United States
Facility Name
University of Texas Health Science Center
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
Wojskowy Instytut Medyczny
City
Warszawa
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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