Kidney Failure, ChronicPhase 3NCT00319150
REPEAT Study - Resistance to ErythroPoietin Effectiveness Algorithm Trial
A Phase 3 study testing erythropoietin in people with Kidney Failure, Chronic and Drug Resistance, run by Queen's University at 7 sites in Canada.
Trial summary
A strategy for optimizing erythropoietin therapy in patients with erythropoietin resistance. A multi-centered, open-label, randomized, controlled trial. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Kidney Failure, Chronic, Drug Resistance
- What is being tested?
- erythropoietin
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 6 participants
- Where
- 7 sitesCanada
- Study dates
- Oct 2006to Feb 2009
- Phase
- Phase 3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- written informed consent
- Adult patients > 18 years old with current Epoetin Alpha dose >250 units/kg/wk
- Hemoglobin >90g/L or <130g/L
- Patients whom a temporary fall in Hb of up to 10g/L is deemed safe
- Patients not expected to have a change in the type of Epo or route of Epo therapy for the duration of the Study period
Who cannot join
- Known iron deficiency (% saturation <20 or ferritin <100)
- Vit B12 or folate deficiency (levels below normal limit for centre lab)
- Known malignancy (solid organ, leukemia or multiple myeloma)
- Jehovah's witness patients/those who refuse transfusion
- Expected to die in the next 6 months
- On dialysis less than 3 months
Show all 13Show fewer
- Temporary (not tunneled) dialysis access catheter
- Pure red cell aplasia
- High likelihood of early withdrawal or interruption of the study (eg. severe or unstable coronary artery disease, stroke, severe liver disease within the 12 weeks before screening)
- Planned major elective surgery during the study period
- Pregnancy or breast-feeding
- Women of child-bearing potential without effective contraception (abstinence, oral contraceptives, diaphragm, IUD)
- Administration of another investigational drug within 4 weeks before screening or planned during study period
Trial locations and contacts
7 sites in 1 country.
7 sites in 1 country
Canada7 sites
Foothills Hospital
Calgary, Alberta
Kingston General Hospital
Kingston, Ontario
London Helath Sciences Centre
London, Ontario
Memorial University Medical Centre
St. John's, Newfoundland and Labrador
Humber River Regional Hosptial
Toronto, Ontario
St. Michael's Hospital
Toronto, Ontario
St. Paul's Hospital
Vancouver, British Columbia
About this study
Official title: Resistance to ErythroPoietin Effectiveness Algorithm Trial
A strategy for optimizing erythropoietin therapy in patients with erythropoietin resistance. A multi-centered, open-label, randomized, controlled trial.
Read the detailed description
Study Rationale
Many treatable causes of erythropoietin resistance (also known as erythropoietin hypo-responsiveness) exist in patients with chronic kidney disease (CKD) stages 3 to 5 . Well recognized causes of erythropoietin resistance include iron deficiency, severe hyperparathyroidism, chronic infection, vitamin deficiency, aluminum toxicity and poor dialysis adequacy. Furthermore, many diseases resulting in the chronic inflammatory state have also been associated with erythropoietin resistance in Non-CKD patients with diseases such as chronic congestive heart failure, chronic liver disease and many connective tissue diseases including rheumatoid arthritis and systemic lupus.
It is now well recognized that CKD stage 5 patients receiving dialysis may also be at risk of developing chronic inflammation resulting in a more severe syndrome characterized by malnutrition and resistance to exogenous erythropoietin replacement therapy. Markers of a chronic inflammatory state that are observed in dialysis patients include hypoalbuminemia, elevated C-reactive protein (CRP), elevated ferritin, increased serum amyloid A and low transferrin saturation. In addition, pro-inflammatory cytokines such as interleukin 6 (IL-6), tumour necrosis factor alpha (TNF-alpha) and interleukin 1 (IL-1) have been shown in vivo to suppress erythroid colony forming units. Erythrocyte lifespan can also be shortened through increased clearance by macrophages that are activated by inflammatory signals and immunoglobulin coated erythrocytes.
Inflammation also affects iron metabolism at many levels. Inflammatory cytokines can lead to reduced serum concentrations of iron and transferrin. Reduction in transferrin then leads to decreased iron absorption via the gut. Lactoferrin in polymorphonuclear cells can act as an iron scavenger with bactericidal activity. Lactoferrin levels have been shown to increase in inflammation and can bind large amounts of free iron, thereby reducing overall availability. Functional iron deficiency, which is also a characteristic the inflammatory state associated with erythropoietin resistance is defined as low availability of iron for erythropoiesis despite normal or high iron stores. Functional iron deficiency can occur in two ways; when high doses of exogenous erythropoietin stimulate erythropoiesis and it exceeds the capacity to deliver adequate iron or alternatively, when delivery of iron from the reticuloendothelial system to hematopoietic cells is blocked. Both mechanisms may occur in patients with chronic inflammation and erythropoietin resistance.
Erythropoietin resistance has been defined in several ways. In studies that analyzed Eprex® use, authors have utilized a dose cut off point of >200units of Eprex®/kg/week as a reasonable marker of 'true' erythropoietin resistance, or erythropoietin resistance occurring with no obvious cause contributing to a poor Eprex® response. Other authors have used the dose cut point of >300units /kg/week to define erythropoietin resistance. Furthermore, a measure of erythropoietin resistance called the Eprex® dose to hematocrit ratio (Eprex®/Hct) has been used as a continuous variable in some studies and has been shown to be positively correlated with certain markers of erythropoietin resistance.
Markers of erythropoietin resistance in dialysis patients have been studied. Previous studies have shown that CRP levels greater than 20mg/L are associated with Eprex® resistance in dialysis patients. Other markers include low albumin, high fibrinogen, low transferrin and high ferritin. Other novel markers of inflammation such as plasma N-acetyl-seryl-aspartyl-lysyl-proline, procalcitonin, fetuin and neopterin have also been studied.
The true prevalence of Eprex® resistance is not known in Canada. It is estimated to be approximately 10% based on the early Eprex® therapy trials. The Canadian Nephrology Practice Patterns Study (CNPPS), which collected data on a large subset of Canadian dialysis patients from 1995 to 1998 provides some further estimates. Several authors have analyzed the CNPPS data and applied Eprex® resistance measures to this study population. Using the dose cut off point of >200units/kg/week of Eprex®, the authors found that the prevalence of Eprex® resistance was 15.7% for hemodialysis (HD) patients and 5.5% for peritoneal dialysis (PD) patients. Further analysis using the Eprex®/Hct measure showed a significant negative correlation between Eprex®/Hct and serum albumin in both HD and PD patients. Body mass index (BMI) was also positively correlated with Eprex®/Hct in both groups. This study also found that when the dose cut off of >200units/kg/week was utilized as a measure of exogenous erythropoietin resistance, 15% of the HD patients above this cut off point were utilizing 34% of all the Eprex® administered to HD patients in the study period. Similarly, 5.5% of Eprex® resistant PD patients required 16.2% of all the Eprex® given to PD patients during the same period.
Little is known about the optimal way to manage 'true' erythropoietin resistance or erythropoietin hypo-responsiveness. Traditionally, nephrologists have overcome erythropoietin resistance by prescribing large or escalating Eprex® doses over prolonged periods of time. There is minimal data that suggests the optimal way to manage these patients. There are no published protocols that have studied systematic increases or decreases in Eprex® in such patients. Furthermore, there are few studies on the safety of the use of high dose Eprex® over prolonged periods of time. It is not known whether a dose ceiling beyond which Eprex® is no longer pharmacologically effective exists in patients with 'true' Eprex® resistance. Studies into the cost effectiveness of high dose Eprex® therapy in Eprex® resistant patients are limited.
Patients with Eprex® resistance may be able to maintain their hemoglobin levels on reduced dose Eprex®, but evidence for the efficacy and safety of an Eprex® dose reduction protocol is limited to small open-label studies. In contradistinction, perhaps escalating Eprex® doses to a maximum dose well above the recommended clinical practice guideline target is what is required to improve hemoglobin levels in these patients.
- Conditions
- Kidney Failure, Chronic, Drug Resistance
- Being tested
- erythropoietin
- Keywords
- Erythropoetin resistance, End Stage Renal Disease on hemodialysis
- Medical subject headings
- Kidney Failure, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
erythropoietinDrug
Also called Epo
Decrease dosage by 12.5% q 2 weeks according to an algorithm.
| Study group | Role | What they receive |
|---|---|---|
| Standard of Care | No intervention | Epo dose to remain constant throughout study |
| Dosage Decrease Arm | Active comparator | Arm 2 is to have an decrease of erythropoietin at regular intervals. Receives: Drug: erythropoietin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary End-points:
Measured: December 31, 2009
Eprex® dose at the completion of the study period
Measured: December 31, 2009
Hemoglobin at completion of the study period (average of last 2 Hb measurements)
Measured: December 31, 2009
Secondary outcomes (5)
Number of transfusions of packed red cells
Measured: December 31, 2009
# of active infections during the study period (active infection is defined in Appendix B)
Measured: December 31, 2009
Hospitalization
Measured: December 31, 2009
Difference in HRQOL scores using Renal SF-36 scores taken at study start and completion study completion
Measured: December 31, 2009
Death
Measured: December 31, 2009
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Apr 2006 (estimated)
- Study startOct 2006
- Primary completionFeb 2009
- Study completionFeb 2009
Why it stopped: New evidence and trouble recruiting
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Kidney Failure, ChronicStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 6 participants (actual)
Sponsor and investigators
- Lead sponsor
- Queen's University
- Sponsor type
- University, hospital or other
- Collaborators
- Ortho Biotech, Inc.
- Investigators
- Karen E Yeates, MD, FRCP(C), MPH, Principal investigator, Queens University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00319150
- Sponsor's protocol ID
- DMED-852-05
- Status last verified
- Feb 2009
- First submitted
- 26 Apr 2006
- Last updated
- 12 Feb 2009
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 12 Feb 2009. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Resistance to ErythroPoietin Effectiveness Algorithm Trial
- ClinicalTrials.gov ID
- NCT00319150
- Acronym / sponsor ID
- DMED-852-05
- Conditions
- Kidney Failure, Chronic, Drug Resistance
- Keywords
- Erythropoetin resistance, End Stage Renal Disease on hemodialysis
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: New evidence and trouble recruiting
- Enrolment
- 6 participants (actual)
- Lead sponsor
- Queen's UniversityUniversity, hospital or other
- Collaborators
- Ortho Biotech, Inc.
- Study start
- Oct 2006
- Primary completion
- Feb 2009 (actual)
- Study completion
- Feb 2009 (actual)
- First posted
- 27 Apr 2006 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A strategy for optimizing erythropoietin therapy in patients with erythropoietin resistance. A multi-centered, open-label, randomized, controlled trial.
Detailed description
Study Rationale
Many treatable causes of erythropoietin resistance (also known as erythropoietin hypo-responsiveness) exist in patients with chronic kidney disease (CKD) stages 3 to 5 . Well recognized causes of erythropoietin resistance include iron deficiency, severe hyperparathyroidism, chronic infection, vitamin deficiency, aluminum toxicity and poor dialysis adequacy. Furthermore, many diseases resulting in the chronic inflammatory state have also been associated with erythropoietin resistance in Non-CKD patients with diseases such as chronic congestive heart failure, chronic liver disease and many connective tissue diseases including rheumatoid arthritis and systemic lupus.
It is now well recognized that CKD stage 5 patients receiving dialysis may also be at risk of developing chronic inflammation resulting in a more severe syndrome characterized by malnutrition and resistance to exogenous erythropoietin replacement therapy. Markers of a chronic inflammatory state that are observed in dialysis patients include hypoalbuminemia, elevated C-reactive protein (CRP), elevated ferritin, increased serum amyloid A and low transferrin saturation. In addition, pro-inflammatory cytokines such as interleukin 6 (IL-6), tumour necrosis factor alpha (TNF-alpha) and interleukin 1 (IL-1) have been shown in vivo to suppress erythroid colony forming units. Erythrocyte lifespan can also be shortened through increased clearance by macrophages that are activated by inflammatory signals and immunoglobulin coated erythrocytes.
Inflammation also affects iron metabolism at many levels. Inflammatory cytokines can lead to reduced serum concentrations of iron and transferrin. Reduction in transferrin then leads to decreased iron absorption via the gut. Lactoferrin in polymorphonuclear cells can act as an iron scavenger with bactericidal activity. Lactoferrin levels have been shown to increase in inflammation and can bind large amounts of free iron, thereby reducing overall availability. Functional iron deficiency, which is also a characteristic the inflammatory state associated with erythropoietin resistance is defined as low availability of iron for erythropoiesis despite normal or high iron stores. Functional iron deficiency can occur in two ways; when high doses of exogenous erythropoietin stimulate erythropoiesis and it exceeds the capacity to deliver adequate iron or alternatively, when delivery of iron from the reticuloendothelial system to hematopoietic cells is blocked. Both mechanisms may occur in patients with chronic inflammation and erythropoietin resistance.
Erythropoietin resistance has been defined in several ways. In studies that analyzed Eprex® use, authors have utilized a dose cut off point of >200units of Eprex®/kg/week as a reasonable marker of 'true' erythropoietin resistance, or erythropoietin resistance occurring with no obvious cause contributing to a poor Eprex® response. Other authors have used the dose cut point of >300units /kg/week to define erythropoietin resistance. Furthermore, a measure of erythropoietin resistance called the Eprex® dose to hematocrit ratio (Eprex®/Hct) has been used as a continuous variable in some studies and has been shown to be positively correlated with certain markers of erythropoietin resistance.
Markers of erythropoietin resistance in dialysis patients have been studied. Previous studies have shown that CRP levels greater than 20mg/L are associated with Eprex® resistance in dialysis patients. Other markers include low albumin, high fibrinogen, low transferrin and high ferritin. Other novel markers of inflammation such as plasma N-acetyl-seryl-aspartyl-lysyl-proline, procalcitonin, fetuin and neopterin have also been studied.
The true prevalence of Eprex® resistance is not known in Canada. It is estimated to be approximately 10% based on the early Eprex® therapy trials. The Canadian Nephrology Practice Patterns Study (CNPPS), which collected data on a large subset of Canadian dialysis patients from 1995 to 1998 provides some further estimates. Several authors have analyzed the CNPPS data and applied Eprex® resistance measures to this study population. Using the dose cut off point of >200units/kg/week of Eprex®, the authors found that the prevalence of Eprex® resistance was 15.7% for hemodialysis (HD) patients and 5.5% for peritoneal dialysis (PD) patients. Further analysis using the Eprex®/Hct measure showed a significant negative correlation between Eprex®/Hct and serum albumin in both HD and PD patients. Body mass index (BMI) was also positively correlated with Eprex®/Hct in both groups. This study also found that when the dose cut off of >200units/kg/week was utilized as a measure of exogenous erythropoietin resistance, 15% of the HD patients above this cut off point were utilizing 34% of all the Eprex® administered to HD patients in the study period. Similarly, 5.5% of Eprex® resistant PD patients required 16.2% of all the Eprex® given to PD patients during the same period.
Little is known about the optimal way to manage 'true' erythropoietin resistance or erythropoietin hypo-responsiveness. Traditionally, nephrologists have overcome erythropoietin resistance by prescribing large or escalating Eprex® doses over prolonged periods of time. There is minimal data that suggests the optimal way to manage these patients. There are no published protocols that have studied systematic increases or decreases in Eprex® in such patients. Furthermore, there are few studies on the safety of the use of high dose Eprex® over prolonged periods of time. It is not known whether a dose ceiling beyond which Eprex® is no longer pharmacologically effective exists in patients with 'true' Eprex® resistance. Studies into the cost effectiveness of high dose Eprex® therapy in Eprex® resistant patients are limited.
Patients with Eprex® resistance may be able to maintain their hemoglobin levels on reduced dose Eprex®, but evidence for the efficacy and safety of an Eprex® dose reduction protocol is limited to small open-label studies. In contradistinction, perhaps escalating Eprex® doses to a maximum dose well above the recommended clinical practice guideline target is what is required to improve hemoglobin levels in these patients.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard of Care | No intervention | –Epo dose to remain constant throughout study |
| Dosage Decrease Arm | Active comparator | Drug: erythropoietinArm 2 is to have an decrease of erythropoietin at regular intervals. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- written informed consent
- Adult patients > 18 years old with current Epoetin Alpha dose >250 units/kg/wk
- Hemoglobin >90g/L or <130g/L
- Patients whom a temporary fall in Hb of up to 10g/L is deemed safe
- Patients not expected to have a change in the type of Epo or route of Epo therapy for the duration of the Study period
Key exclusion criteria (13 listed)
- Known iron deficiency (% saturation <20 or ferritin <100)
- Vit B12 or folate deficiency (levels below normal limit for centre lab)
- Known malignancy (solid organ, leukemia or multiple myeloma)
- Jehovah's witness patients/those who refuse transfusion
- Expected to die in the next 6 months
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| erythropoietinAlso: EpoDecrease dosage by 12.5% q 2 weeks according to an algorithm. | Drug | Dosage Decrease Arm |
Primary outcome
Primary End-points:
Time frame: December 31, 2009
Eprex® dose at the completion of the study period
Time frame: December 31, 2009
Hemoglobin at completion of the study period (average of last 2 Hb measurements)
Time frame: December 31, 2009
5 secondary outcomes
Number of transfusions of packed red cells
Time frame: December 31, 2009
# of active infections during the study period (active infection is defined in Appendix B)
Time frame: December 31, 2009
Hospitalization
Time frame: December 31, 2009
Difference in HRQOL scores using Renal SF-36 scores taken at study start and completion study completion
Time frame: December 31, 2009
Death
Time frame: December 31, 2009
Results and safety
The study was stopped early (reason given: New evidence and trouble recruiting). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Feb 2009.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Karen E Yeates, MD, FRCP(C), MPH principal investigator
Queens University
7 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing erythropoietin in people with Kidney Failure, Chronic and Drug Resistance, run by Queen's University at 7 sites in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 12 Feb 2009. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 7 sites in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: New evidence and trouble recruiting). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Primary End-points: (time frame: December 31, 2009). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Feb 2009; AzTrials last refreshed its copy on 30 Oct 2026.