Disorder of Transplanted KidneyPhase 3NCT01436747
Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients
A Phase 3 study testing Paricalcitol in people with Disorder of Transplanted Kidney and Proteinuria, run by University Medical Centre Ljubljana at 1 site in Slovenia.
Trial summary
The study 'Safety and Efficacy of Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients' is designed to assess the effects of paricalcitol in kidney transplant recipients with proteinuria. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Disorder of Transplanted Kidney, Proteinuria, Albuminuria
- What is being tested?
- Paricalcitol
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 168 participants
- Where
- 1 siteSlovenia
- Study dates
- Jul 2012to Jul 2015
- 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
- Recipients of a deceased donor kidney transplant at least 3 months after transplantation
- Urinary protein to creatinine ratio (UPCR) > 200 mg/g (20 mg/mmol) as determined by the the mean of three second morning void urine specimens
- Subject is on stable immunosuppression for at least 3 months
- Subject is on stable doses of antihypertensive medications for at least 3 months
- Subject is not expected to begin dialysis for at least 6 months
- Estimated glomerular filtration rate > 15 ml/min/1.73 m2
- Corrected serum calcium level < 2.6 mmol/l
- Intact parathormone value > 30 pg/ml
Who cannot join
- Subjects on vitamin D receptor activation therapy within 3 months prior to the first study visit
- Acute kidney injury within 3 months of the first study visit
- Subjects with poorly controlled hypertension
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Efficacy and Safety of Selective Vitamin D Receptor Activation With Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients: a Randomized Controlled Trial
The study 'Safety and Efficacy of Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients' is designed to assess the effects of paricalcitol in kidney transplant recipients with proteinuria.
It is a single centre, randomized, placebo-controlled, double-blind clinical trial that tests the hypothesis that 24 weeks' treatment with paricalcitol compared to placebo will result in a decrease in urinary protein excretion in recipients of a kidney transplant at least three months after transplantation. Additionally, the effects of paricalcitol on albuminuria, estimated glomerular filtration rate, and blood pressure will be investigated.
Read the detailed description
Kidney transplantation is the treatment of choice for end-stage renal disease patients. In comparison to dialysis it offers longer survival and better quality of life to certain patients with end stage renal disease. In the last two decades, short-term (i.e. 1- and 3-year) kidney transplant survival has increased significantly and is currently exceeding 90% in state-of-the-art transplant centers. This is considered to be due to the safe and effective immunosuppressive therapy in the early post-transplant period, and to the careful management of patients with chronic renal disease (CRD) before and after the transplantation. In spite of the progress described above, long-term (i.e. 5- and 10-year) transplant survival has not significantly improved over the recent decades. Two main causes for long-term loss of transplanted kidneys are the development of the transplant chronic kidney disease (CKD) (i.e. chronic allograft nephropathy) and patient death with a functioning transplant due to cardiovascular events.
Proteinuria (> 150 mg of proteins in urine per day) is a manifestation of kidney disease and is an important risk factor for CKD progression. This applies also to kidney transplant recipients. Studies have shown that proteinuria is present in 20-40% of transplanted patients. According to observational studies, proteinuria is an independent predictor for CKD progression and transplant failure, as well as of increased risk for cardiovascular events. In CKD patients, treatment with renin-angiotensin-aldosterone system inhibitors (RAAS - angiotensin converting enzyme inhibitors, angiotensin receptor blockers, aldosterone receptor blockers) reduces proteinuria and thus slows the renal disease progression. In spite of the demonstrated renoprotective effect of RAAS inhibitors, the risk for CKD progression remains high. Furthermore, large epidemiological studies have not shown clinically significant effect of RAAS inhibitor therapy on the reduction of cardiovascular risk. In spite of an optimal RAAS inhibitor therapy, renal and cardiovascular diseases continue to progress, which is also associated with persistent proteinuria. Therefore, new treatment modalities to reduce proteinuria with consequent delay in the progression of CKD and cardiovascular disease are being sought.
Calcitriol is an active form of vitamin D produced in the kidneys. It is important for calcium and phosphate metabolism, as well as for bone mineralization. Decreasing blood calcitriol levels are associated with declining renal function. Decreased calcitriol levels in patients with CKD contribute to the development of secondary hyperparathyroidism. Furthermore, calcitriol deficiency is associated with increased proteinuria and further progression of renal impairment. Vitamin D deficiency in patients with end stage renal disease is also related to higher cardiovascular mortality. The pleiotropic effects of calcitriol probably reflect the presence of vitamin D receptors in different tissues; it is via these receptors that calcitriol exerts its pharmacological effects. Vitamin D receptors have been found not only in kidneys and bones, but also in the cells of the myocardium, in the vascular endothelium, the endocrine part of the pancreas, the intestine and the prostate.
Treatment with an analogue of the active vitamin D form, paricalcitol, significantly reduced proteinuria and slowed progression of renal disease in animal models as well as in patients with CKD, particularly in patients diabetes and diabetic nephropathy. This is considered to be due to the positive effect of paricalcitol on RAAS inhibition in the kidneys, which is independent of calcium and parathormone metabolism. Reduced proteinuria leads to a reduced inflammatory response, preservation of the glomerular basement membrane structure and slowing of glomerulosclerosis.
The positive effects of paricalcitol on the reduction of proteinuria observed in patients with CKD may also be important for kidney transplant recipients: by reducing the proteinuria, progression of CKD in the transplanted kidney might be delayed and the risk for cardiovascular events reduced. This might contribute to the improvement of long-term kidney transplant survival, which has not changed significantly in the last two decades.
This study tests the hypothesis whether paricalcitol persistently reduces proteinuria in kidney transplant recipients.
- Conditions
- Disorder of Transplanted Kidney, Proteinuria, Albuminuria
- Being tested
- Paricalcitol, Placebo
- Keywords
- Kidney transplantation, Proteinuria, Albuminuria, Vitamin D, Paricalcitol
- Medical subject headings
- Proteinuria, Albuminuria
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ParicalcitolDrug
Also called Zemplar
2 micrograms daily, peroral, 24 weeks
PlaceboDrug
2 micrograms daily, peroral, 24 weeks
| Study group | Role | What they receive |
|---|---|---|
| Paricalcitol | Active comparator | Not described Receives: Drug: Paricalcitol |
| Matching placebo | Placebo comparator | Not described Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
The percentage change in urinary protein to creatinine ratio (UPCR) from baseline to the last measurement during treatment.
Measured: baseline and 6 months
Secondary outcomes (4)
The percentage change in urinary albumin to creatinine ratio (UACR) from baseline to the last measurement during treatment.
Measured: baseline and 6 months
Change in 24-hour urinary protein excretion form baseline to the last measurement during treatment.
Measured: baseline and 6 months
The proportion of patients achieving at least a 15 mg/mmol reduction in the last on-treatment UPCR level from the baseline.
Measured: baseline and 6 months
Change in estimated glomerular filtration rate, blood pressure and biomarkers, including (but not limited to) C-reactive protein, plasma renin activity, aldosterone.
Measured: baseline and 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Sep 2011 (estimated)
- Study startJul 2012
- Primary completionOct 2014
- Study completionJul 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Disorder of Transplanted KidneyStudies of the same condition, open and under way.
- More trials run by University Medical Centre LjubljanaThe sponsor's other registered studies.
- 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
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 168 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Medical Centre Ljubljana
- Sponsor type
- University, hospital or other
- Collaborators
- Abbott
- Responsible party
- Principal investigator, Miha Arnol, M.D., Ph.D., University Medical Centre Ljubljana
- Investigators
- Miha Arnol, M.D., Ph.D., Principal investigator, University Medical Centre Ljubljana, Department of NephrologyAljoša Kandus, M.D., Ph.D., Study chair, University Medical Centre Ljubljana, Department of Nephrology
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01436747
- Sponsor's protocol ID
- 31-06-2011
- Status last verified
- Dec 2017
- First submitted
- 14 Sep 2011
- Last updated
- 27 Dec 2017
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Arnol M, Oblak M, Mlinsek G, Bren AF, Buturović-Ponikvar J, Kandus A. Proteinuria in kidney transplant recipients: prevalence in a national cohort and study design of the effect of paricalcitol for reduction of proteinuria. Transplant International 2011; 24(2): 185(A204).
Oblak M, Mlinsek G, Kandus A, Buturovic-Ponikvar J, Arnol M. Paricalcitol versus placebo for reduction of proteinuria in kidney transplant recipients: a double-blind, randomized controlled trial. Transpl Int. 2018 Dec;31(12):1391-1404. doi: 10.1111/tri.13323. Epub 2018 Aug 20.
PubMed 30062716
Study at a glance
From the registry record, last updated by the sponsor on 27 Dec 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy and Safety of Selective Vitamin D Receptor Activation With Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients: a Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT01436747
- Acronym / sponsor ID
- 31-06-2011
- Conditions
- Disorder of Transplanted Kidney, Proteinuria, Albuminuria
- Keywords
- Kidney transplantation, Proteinuria, Albuminuria, Vitamin D, Paricalcitol
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 168 participants (actual)
- Lead sponsor
- University Medical Centre LjubljanaUniversity, hospital or other
- Collaborators
- Abbott
- Study start
- Jul 2012
- Primary completion
- Oct 2014 (actual)
- Study completion
- Jul 2015 (actual)
- First posted
- 20 Sep 2011 (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.
The study 'Safety and Efficacy of Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients' is designed to assess the effects of paricalcitol in kidney transplant recipients with proteinuria.
It is a single centre, randomized, placebo-controlled, double-blind clinical trial that tests the hypothesis that 24 weeks' treatment with paricalcitol compared to placebo will result in a decrease in urinary protein excretion in recipients of a kidney transplant at least three months after transplantation. Additionally, the effects of paricalcitol on albuminuria, estimated glomerular filtration rate, and blood pressure will be investigated.
Detailed description
Kidney transplantation is the treatment of choice for end-stage renal disease patients. In comparison to dialysis it offers longer survival and better quality of life to certain patients with end stage renal disease. In the last two decades, short-term (i.e. 1- and 3-year) kidney transplant survival has increased significantly and is currently exceeding 90% in state-of-the-art transplant centers. This is considered to be due to the safe and effective immunosuppressive therapy in the early post-transplant period, and to the careful management of patients with chronic renal disease (CRD) before and after the transplantation. In spite of the progress described above, long-term (i.e. 5- and 10-year) transplant survival has not significantly improved over the recent decades. Two main causes for long-term loss of transplanted kidneys are the development of the transplant chronic kidney disease (CKD) (i.e. chronic allograft nephropathy) and patient death with a functioning transplant due to cardiovascular events.
Proteinuria (> 150 mg of proteins in urine per day) is a manifestation of kidney disease and is an important risk factor for CKD progression. This applies also to kidney transplant recipients. Studies have shown that proteinuria is present in 20-40% of transplanted patients. According to observational studies, proteinuria is an independent predictor for CKD progression and transplant failure, as well as of increased risk for cardiovascular events. In CKD patients, treatment with renin-angiotensin-aldosterone system inhibitors (RAAS - angiotensin converting enzyme inhibitors, angiotensin receptor blockers, aldosterone receptor blockers) reduces proteinuria and thus slows the renal disease progression. In spite of the demonstrated renoprotective effect of RAAS inhibitors, the risk for CKD progression remains high. Furthermore, large epidemiological studies have not shown clinically significant effect of RAAS inhibitor therapy on the reduction of cardiovascular risk. In spite of an optimal RAAS inhibitor therapy, renal and cardiovascular diseases continue to progress, which is also associated with persistent proteinuria. Therefore, new treatment modalities to reduce proteinuria with consequent delay in the progression of CKD and cardiovascular disease are being sought.
Calcitriol is an active form of vitamin D produced in the kidneys. It is important for calcium and phosphate metabolism, as well as for bone mineralization. Decreasing blood calcitriol levels are associated with declining renal function. Decreased calcitriol levels in patients with CKD contribute to the development of secondary hyperparathyroidism. Furthermore, calcitriol deficiency is associated with increased proteinuria and further progression of renal impairment. Vitamin D deficiency in patients with end stage renal disease is also related to higher cardiovascular mortality. The pleiotropic effects of calcitriol probably reflect the presence of vitamin D receptors in different tissues; it is via these receptors that calcitriol exerts its pharmacological effects. Vitamin D receptors have been found not only in kidneys and bones, but also in the cells of the myocardium, in the vascular endothelium, the endocrine part of the pancreas, the intestine and the prostate.
Treatment with an analogue of the active vitamin D form, paricalcitol, significantly reduced proteinuria and slowed progression of renal disease in animal models as well as in patients with CKD, particularly in patients diabetes and diabetic nephropathy. This is considered to be due to the positive effect of paricalcitol on RAAS inhibition in the kidneys, which is independent of calcium and parathormone metabolism. Reduced proteinuria leads to a reduced inflammatory response, preservation of the glomerular basement membrane structure and slowing of glomerulosclerosis.
The positive effects of paricalcitol on the reduction of proteinuria observed in patients with CKD may also be important for kidney transplant recipients: by reducing the proteinuria, progression of CKD in the transplanted kidney might be delayed and the risk for cardiovascular events reduced. This might contribute to the improvement of long-term kidney transplant survival, which has not changed significantly in the last two decades.
This study tests the hypothesis whether paricalcitol persistently reduces proteinuria in kidney transplant recipients.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Paricalcitol | Active comparator | Drug: Paricalcitol |
| Matching placebo | Placebo comparator | Drug: Placebo |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- Recipients of a deceased donor kidney transplant at least 3 months after transplantation
- Urinary protein to creatinine ratio (UPCR) > 200 mg/g (20 mg/mmol) as determined by the the mean of three second morning void urine specimens
- Subject is on stable immunosuppression for at least 3 months
- Subject is on stable doses of antihypertensive medications for at least 3 months
- Subject is not expected to begin dialysis for at least 6 months
Key exclusion criteria (3 listed)
- Subjects on vitamin D receptor activation therapy within 3 months prior to the first study visit
- Acute kidney injury within 3 months of the first study visit
- Subjects with poorly controlled hypertension
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 |
|---|---|---|
| ParicalcitolAlso: Zemplar2 micrograms daily, peroral, 24 weeks | Drug | Paricalcitol |
| Placebo2 micrograms daily, peroral, 24 weeks | Drug | Matching placebo |
Primary outcome
The percentage change in urinary protein to creatinine ratio (UPCR) from baseline to the last measurement during treatment.
Time frame: baseline and 6 months
4 secondary outcomes
The percentage change in urinary albumin to creatinine ratio (UACR) from baseline to the last measurement during treatment.
Time frame: baseline and 6 months
Change in 24-hour urinary protein excretion form baseline to the last measurement during treatment.
Time frame: baseline and 6 months
The proportion of patients achieving at least a 15 mg/mmol reduction in the last on-treatment UPCR level from the baseline.
Time frame: baseline and 6 months
Change in estimated glomerular filtration rate, blood pressure and biomarkers, including (but not limited to) C-reactive protein, plasma renin activity, aldosterone.
Time frame: baseline and 6 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Dec 2017.
- BackgroundArnol M, Oblak M, Mlinsek G, Bren AF, Buturović-Ponikvar J, Kandus A. Proteinuria in kidney transplant recipients: prevalence in a national cohort and study design of the effect of paricalcitol for reduction of proteinuria. Transplant International 2011; 24(2): 185(A204).
- Derived from this study: PubMed 30062716Oblak M, Mlinsek G, Kandus A, Buturovic-Ponikvar J, Arnol M. Paricalcitol versus placebo for reduction of proteinuria in kidney transplant recipients: a double-blind, randomized controlled trial. Transpl Int. 2018 Dec;31(12):1391-1404. doi: 10.1111/tri.13323. Epub 2018 Aug 20.
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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.
Miha Arnol, M.D., Ph.D. principal investigator
University Medical Centre Ljubljana, Department of Nephrology
Aljoša Kandus, M.D., Ph.D. study chair
University Medical Centre Ljubljana, Department of Nephrology
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Paricalcitol in people with Disorder of Transplanted Kidney and Proteinuria, run by University Medical Centre Ljubljana at 1 site in Slovenia.
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 8 inclusion and 3 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: finished, as of the sponsor's last update on 27 Dec 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Slovenia. 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. Some participants in this study may receive a placebo. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
The percentage change in urinary protein to creatinine ratio (UPCR) from baseline to the last measurement during treatment. (time frame: baseline and 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01436747, which also lists 2 linked publications.
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 27 Dec 2017.