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Safety and Efficacy Study of the Effect of Etanercept in Hemodialysis Patients

Primary Purpose

End Stage Renal Disease

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Etanercept
Placebo
Sponsored by
Kaysen, George A., M.D., Ph.D.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End Stage Renal Disease focused on measuring etanercept, malnutrition, inflammation, hemodialysis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Presence of end stage renal disease Exclusion Criteria: History of Tuberculosis History of Recurrent Infection Recent AMI, Cancer within previous 5 years Presence of Hepatitis B, Hepatitis C, HIV, systemic lupus erythematosis, presence of transcutaneous access (external catheter)

Sites / Locations

  • University of California, Davis, Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Etanercept 25 mg

Saline

Arm Description

Etanercept 25 mg injection twice a week

Saline injection twice a week

Outcomes

Primary Outcome Measures

Albumin
An increased serum albumin (ALB) concentration expected. Higher concentrations of Albumin indicate better outcome. Normal ranges of Albumin in this study is from 3.5 to 5.5 gram per deciliter (g/dL). We expect ALB to remain or increase in this study.
C-reactive Protein
A reduced C-reactive protein (CRP) concentration is expected.

Secondary Outcome Measures

Prealbumin (mg/dL)
Effect of treatment on prealbumin (PAB) concentration

Full Information

First Posted
February 15, 2006
Last Updated
July 12, 2021
Sponsor
Kaysen, George A., M.D., Ph.D.
Collaborators
Amgen, Dialysis Clinic, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00293202
Brief Title
Safety and Efficacy Study of the Effect of Etanercept in Hemodialysis Patients
Official Title
The Effect of Etanercept in Suppression of the Systemic Inflammatory Response in Hemodialysis Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Terminated
Why Stopped
We were unable to recruit sufficient patients within the confines of our budget considering the restrains on our recruitment criteria
Study Start Date
January 2005 (Actual)
Primary Completion Date
March 2008 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kaysen, George A., M.D., Ph.D.
Collaborators
Amgen, Dialysis Clinic, Inc.

4. Oversight

5. Study Description

Brief Summary
Etanercept is a novel anti-inflammatory agent currently used in patients with rheumatoid arthritis. We are examining whether Etanercept is effective in improving the nutritional status of hemodialysis patients as a consequence of its ability to decrease inflammation.
Detailed Description
Hemodialysis patients with end stage renal disease have a high mortality rate. In individual patients, mortality is associated with a low serum albumin concentration, a marker of poor nutritional status, and with elevated C-reactive protein, a marker of inflammation. Since efforts to improve nutrition through dietary intake have not been successful, inflammation is thought to play a key role in determining nutritional status. Recently, it has been shown that malnutrition, inflammation, and atherosclerosis are closely related in patients with chronic renal failure. It is our hypothesis that suppression of the cycle of inflammation, malnutrition, and vascular injury caused by atherosclerosis will improve survival in dialysis patients. This study is designed to examine whether suppression of the inflammatory response can be accomplished safely with Etanercept and to determine if this suppression will improve nutritional status and clinical outcome in hemodialysis patients with poor nutritional status and evidence of inflammation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease
Keywords
etanercept, malnutrition, inflammation, hemodialysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
This is a double blind study- one group received 25mg Etanercept twice per week; the other is control - receiving saline twice per week
Masking
ParticipantCare ProviderInvestigator
Masking Description
Double Blind Study
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Etanercept 25 mg
Arm Type
Active Comparator
Arm Description
Etanercept 25 mg injection twice a week
Arm Title
Saline
Arm Type
Placebo Comparator
Arm Description
Saline injection twice a week
Intervention Type
Drug
Intervention Name(s)
Etanercept
Other Intervention Name(s)
Enbrel
Intervention Description
Hemodialysis patients will receive Etanercept at a dose of 25 mg by subcutaneous injection twice a week
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Saline
Intervention Description
Hemodialysis patients will receive Saline by subcutaneous injection twice a week
Primary Outcome Measure Information:
Title
Albumin
Description
An increased serum albumin (ALB) concentration expected. Higher concentrations of Albumin indicate better outcome. Normal ranges of Albumin in this study is from 3.5 to 5.5 gram per deciliter (g/dL). We expect ALB to remain or increase in this study.
Time Frame
52 weeks
Title
C-reactive Protein
Description
A reduced C-reactive protein (CRP) concentration is expected.
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
Prealbumin (mg/dL)
Description
Effect of treatment on prealbumin (PAB) concentration
Time Frame
52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Presence of end stage renal disease Exclusion Criteria: History of Tuberculosis History of Recurrent Infection Recent AMI, Cancer within previous 5 years Presence of Hepatitis B, Hepatitis C, HIV, systemic lupus erythematosis, presence of transcutaneous access (external catheter)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
George Kaysen, MD, PhD
Organizational Affiliation
University of California, Davis
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, Davis, Medical Center
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20497755
Citation
Don BR, Kim K, Li J, Dwyer T, Alexander F, Kaysen GA. The effect of etanercept on suppression of the systemic inflammatory response in chronic hemodialysis patients. Clin Nephrol. 2010 Jun;73(6):431-8. doi: 10.5414/cnp73431.
Results Reference
result
Links:
URL
https://pubmed.ncbi.nlm.nih.gov/20497755/
Description
B.R. Don, K.Kim, J. Li, T. Dwyer, F. Alexander and G.A. Kaysen.The effect of etanercept on suppression of the systemic inflammatory response in chronic hemodialysis patients. 2010; 73: 431-438. doi: 10.5414/CNP73431

Learn more about this trial

Safety and Efficacy Study of the Effect of Etanercept in Hemodialysis Patients

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