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CARE-2 (Calcium Acetate [PhosLo®]/Sevelamer[Renagel®] Evaluation Study 2) for Heart Calcification in Dialysis Patients

Primary Purpose

Calcinosis, Arteriosclerosis, Hyperparathyroidism, Secondary

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
calcium acetate
sevelamer
atorvastatin
Sponsored by
Nabi Biopharmaceuticals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Calcinosis focused on measuring PhosLo (Calcium acetate), Renagel (sevelamer, polyallylamine HCL), kidney dialysis, hyperphosphatemia, Kidney failure

Eligibility Criteria

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

Inclusion Criteria: Eligible subjects will be male or female patients with end-stage renal disease on maintenance hemodialysis for less than 5 years, with elevated LDL cholesterol Currently treated with oral phosphate binders Coronary artery calcium scores of 30 to 5000 Agatston units measured by electron beam CT scanning Written informed consent Negative serum pregnancy test if appropriate Expect to comply with protocol procedures and schedule Exclusion Criteria: Unstable angina pectoris Severe congestive heart failure Severe obstructive pulmonary disease requiring supplemental oxygen Severe liver dysfunction Severe malnutrition Severe hyperparathyroidism Known HIV Active malignancy for which the subject is receiving chemotherapy or radiation Planned renal transplant within the next year Clinical evidence of calciphylaxis or recent history of hypercalcemia History of obstructed bowels Hypersensitivity to any of the components of the study medication History of swallowing disorders Weight > 300 pounds Any condition which makes patient participation not in the patient's best interest

Sites / Locations

  • University of Texas Health Sciences Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

PhosLo + atorvastatin

Sevelamer + atorvastatin

Outcomes

Primary Outcome Measures

electron-beam CT coronary artery calcification AGATSTON score

Secondary Outcome Measures

serum phosphorus
calcium x phosphorus product

Full Information

First Posted
September 13, 2005
Last Updated
December 26, 2007
Sponsor
Nabi Biopharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00211939
Brief Title
CARE-2 (Calcium Acetate [PhosLo®]/Sevelamer[Renagel®] Evaluation Study 2) for Heart Calcification in Dialysis Patients
Official Title
CARE-2 (Calcium Acetate (PhosLo®)/Sevelamer(Renagel®) Evaluation Study 2)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2007
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
December 2006 (Actual)
Study Completion Date
March 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Nabi Biopharmaceuticals

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to evaluate the effects of two phosphate binders, PhosLo and sevelamer, on heart calcification in dialysis patients. The study will use a non-invasive technique, electron beam computed tomography (CT) scanning, to measure calcium in the coronary arteries, the aortic valve, and the mitral valve.
Detailed Description
Cardiovascular disease is the major cause of death and disability in patients with end-stage renal disease on hemodialysis. It has been hypothesized that ingestion of calcium-based phosphate binders results in net positive calcium balance and vascular calcium deposition. Chertow et al. tested the role of ingested calcium in the progression of cardiovascular calcification in the Treat-To-Goal study (Kidney International 62:245, 2002). They reported that patients treated with calcium-based phosphate binders demonstrated progressive cardiovascular calcification, while patients treated with a calcium-free binder, sevelamer, showed stabilization or improvement in calcification scores. However, the protocol did not prohibit intake of supplemental oral calcium in the sevelamer group, which confounded their ability to accurately test the calcium hypothesis. Moreover, due to the cholesterol sequestering activities of sevelamer, the low-density lipoprotein (LDL) cholesterol was lower among sevelamer-treated patients than the calcium treated patients, resulting in a major imbalance in a cardiovascular risk factor. Lowering LDL level reduces progression of CVC and therefore confounds interpretation of the study. Subsequently, it has been reported in the lay press that patients randomized to sevelamer or calcium-based binders in the Dialysis Clinical Outcomes Revisited (DCOR) study have failed to show a difference in mortality or major secondary endpoints (Suki et al., To be presented American Society of Nephrology November 2005). To circumvent these limitations, the CARE-2 study will test the hypothesis that if LDL levels are lowered to a similar level in calcium acetate and sevelamer-treated patients, there will be no difference in the progression of cardiac calcification. CARE-2 will randomize patients with elevated LDL to calcium acetate or sevelamer. Atorvastatin is added to achieve LDL < 70 mg/dL in both treatment groups. The primary endpoint is change in cardiac calcification scores, determined by electron beam scanning after 1 year. Secondary endpoints include the ability of calcium acetate and sevelamer to control phosphorus and meet NKF-K/DOQI guidelines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Calcinosis, Arteriosclerosis, Hyperparathyroidism, Secondary
Keywords
PhosLo (Calcium acetate), Renagel (sevelamer, polyallylamine HCL), kidney dialysis, hyperphosphatemia, Kidney failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
203 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
PhosLo + atorvastatin
Arm Title
2
Arm Type
Active Comparator
Arm Description
Sevelamer + atorvastatin
Intervention Type
Drug
Intervention Name(s)
calcium acetate
Other Intervention Name(s)
PhosLo
Intervention Description
667 mg gelcap, 2-4 t.i.d titrated to serum phosphorus level
Intervention Type
Drug
Intervention Name(s)
sevelamer
Other Intervention Name(s)
Renagel
Intervention Description
1-3 tablets t.i.d, titrated to serum phosphorus level
Intervention Type
Drug
Intervention Name(s)
atorvastatin
Other Intervention Name(s)
Lipitor
Intervention Description
20 mg PO qD (in PhosLo group), or held until D60 (sevelamer group); titrate by LDL levels and liver function tests
Primary Outcome Measure Information:
Title
electron-beam CT coronary artery calcification AGATSTON score
Time Frame
change at 12 mo from baseline
Secondary Outcome Measure Information:
Title
serum phosphorus
Time Frame
Days 30-365
Title
calcium x phosphorus product
Time Frame
Days 30-365

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Eligible subjects will be male or female patients with end-stage renal disease on maintenance hemodialysis for less than 5 years, with elevated LDL cholesterol Currently treated with oral phosphate binders Coronary artery calcium scores of 30 to 5000 Agatston units measured by electron beam CT scanning Written informed consent Negative serum pregnancy test if appropriate Expect to comply with protocol procedures and schedule Exclusion Criteria: Unstable angina pectoris Severe congestive heart failure Severe obstructive pulmonary disease requiring supplemental oxygen Severe liver dysfunction Severe malnutrition Severe hyperparathyroidism Known HIV Active malignancy for which the subject is receiving chemotherapy or radiation Planned renal transplant within the next year Clinical evidence of calciphylaxis or recent history of hypercalcemia History of obstructed bowels Hypersensitivity to any of the components of the study medication History of swallowing disorders Weight > 300 pounds Any condition which makes patient participation not in the patient's best interest
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wajeh Y Qunibi, M.D.
Organizational Affiliation
The University of Texas Health Science Center at San Antonio
Official's Role
Study Chair
Facility Information:
Facility Name
University of Texas Health Sciences Center
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229-3900
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
12081584
Citation
Chertow GM, Burke SK, Raggi P; Treat to Goal Working Group. Sevelamer attenuates the progression of coronary and aortic calcification in hemodialysis patients. Kidney Int. 2002 Jul;62(1):245-52. doi: 10.1046/j.1523-1755.2002.00434.x.
Results Reference
background
PubMed Identifier
18423809
Citation
Qunibi W, Moustafa M, Muenz LR, He DY, Kessler PD, Diaz-Buxo JA, Budoff M; CARE-2 Investigators. A 1-year randomized trial of calcium acetate versus sevelamer on progression of coronary artery calcification in hemodialysis patients with comparable lipid control: the Calcium Acetate Renagel Evaluation-2 (CARE-2) study. Am J Kidney Dis. 2008 Jun;51(6):952-65. doi: 10.1053/j.ajkd.2008.02.298. Epub 2008 Apr 18.
Results Reference
derived

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CARE-2 (Calcium Acetate [PhosLo®]/Sevelamer[Renagel®] Evaluation Study 2) for Heart Calcification in Dialysis Patients

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