Renal Transplanted RecipientsPhase 4NCT00371826
SOCRATES: Steroid or Cyclosporine Removal After Transplantation Using Everolimus
A Phase 4 study testing Everolimus (RAD001), Cyclosporine (Calcineurin Inhibitor (CNI)) and Methylprednisone/prednisone in people with Renal Transplanted Recipients, run by Novartis Pharmaceuticals at 7 sites in Australia.
Trial summary
The aim of this study is to assess the safety and efficacy of corticosteroid discontinuation versus cyclosporine micro emulsion discontinuation in recipients receiving reduced exposure cyclosporine micro emulsion and corticosteroids plus enteric-coated mycophenolate sodium (EC-MPS) initially, changed to everolimus at… Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Renal Transplanted Recipients
- What is being tested?
- Everolimus (RAD001), Cyclosporine (Calcineurin Inhibitor (CNI)) and Methylprednisone/prednisone
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 126 participants
- Where
- 7 sitesAustralia
- Study dates
- Mar 2006to Jun 2012
- Phase
- Phase 4
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Males and females aged 18-65 years inclusive.
- First time recipients of cadaveric, living unrelated or living related donor kidney transplants.
- Patients who are willing and able to participate in the study and from whom written informed consent has been obtained.
Who cannot join
- Patients who are recipients of multiple organ transplants, including more than one kidney, kidney and pancreas, or previous transplant with any organ other than kidney.
- Patients at high immunological risk of graft loss, indicated by peak PRA >50% or loss of a previous renal allograft within the first 6 months of transplantation due to acute rejection.
- Patients who have received an investigational drug within 4 weeks prior to the screening visit.
- Presence of any severe allergy or hypersensitivity to drugs similar to everolimus (e.g. antibiotics such as Clindamycin)
- Other protocol-defined inclusion/exclusion criteria may applied
Trial locations and contacts
7 sites in 1 country.
7 sites in 1 country
Australia7 sites
Royal Prince Alfred Hospital
NSW
Westmead Hospital
NSW
Princess Alexandra Hospital
QLD
Monash Medical Centre
Sale
Queen Elizabeth Hospital
Sale
Royal Melbourne Hospital
VIC
Sir Charles Gairdner Hospital
WA
About this study
Official title: A Prospective, Open-label, Controlled Multicenter Trial to Assess the Efficacy and Safety of an Induction Regimen of Cyclosporine Micro Emulsion, Enteric-coated Mycophenolate Sodium (EC-MPS) and Corticosteroids, Followed by Administration of Everolimus and Enteric-coated Mycophenolate Sodium (EC-MPS), With Either the Withdrawal of Cyclosporine Micro Emulsion or Corticosteroids in de Novo Kidney Transplant Recipients
The aim of this study is to assess the safety and efficacy of corticosteroid discontinuation versus cyclosporine micro emulsion discontinuation in recipients receiving reduced exposure cyclosporine micro emulsion and corticosteroids plus enteric-coated mycophenolate sodium (EC-MPS) initially, changed to everolimus at 2 weeks post-transplant. These two groups will be compared to a third control group, who will receive treatment consisting of cyclosporine micro emulsion, enteric-coated mycophenolate sodium (EC-MPS) and steroids.
- Conditions
- Renal Transplanted Recipients
- Being tested
- Everolimus (RAD001), Cyclosporine (Calcineurin Inhibitor (CNI)), Methylprednisone/prednisone, Mycophenolate sodium (MPA)
- Keywords
- Renal transplantation, everolimus, Immunosuppressants
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Everolimus (RAD001)Drug
Also called Certican®
Cyclosporine (Calcineurin Inhibitor (CNI))Drug
Also called Neoral®
Methylprednisone/prednisoneDrug
Mycophenolate sodium (MPA)Drug
Also called myfortic®
| Study group | Role | What they receive |
|---|---|---|
| Calcineurin Inhibitor (CNI) Withdrawal | Experimental | Every randomized patient in this group received
Day 1 - Day 14: cyclosporine as Calcineurin Inhibitor (CNI) 5 mg/kg twice daily (b.i.d.), dose adjusted to achieve C2 target of 1,500 ng/mL (range 1,400-1,600 ng/mL) + mycophenolate sodium (MPA)720 mg b.i.d. + methylprednisone/prednisone 500 mg intra-operatively, 250 mg on day 1, then 10-30 mg/day prednisone
Day 15 - Day 60: everolimus 1.5 mg b.i.d. to achieve target 6-10 ng/mL + cyclosporine decrease dose as per protocol guideline + MPA 720 mg b.i.d. until everolimus trough >6 ng/mL, then MPA was stopped + prednisone 10-30mg/day
Day 61 - Day 120: everolimus dose adjusted to achieve target 6-10 ng/mL + cyclosporine 25% dose reduction per fortnight, to be discontinued by day 120 as per protocol (or commence reduction by day 120 at discretion of investigator, to be completed within 2 months of commencement) + prednisone 10-30mg/day Day 121 - Month 36: everolimus dose adjusted to achieve target 8-12 ng/mL + prednisone 5-10 mg/day Receives: Drug: Everolimus (RAD001); Drug: Cyclosporine (Calcineurin Inhibitor (CNI)); Drug: Methylprednisone/prednisone; Drug: Mycophenolate sodium (MPA) |
| Steroid Withdrawal | Experimental | Every randomized patient in this group received
Day 1 -14: cyclosporine 5 mg/kg b.i.d., dose adjusted to achieve C2 target as per protocol + mycophenolate sodium (MPA) 720 mg b.i.d. + methylprednisone/prednisone 500 mg intra-operatively, 250 mg on day 1, then 10-30 mg prednisone per day
Day 15 - 60: everolimus 1.5 mg b.i.d. to achieve target 6-10 ng/mL + cyclosporine decrease dose as per protocol guideline + MPA 720 mg b.i.d. until everolimus trough >6 ng/mL, then MPA was stopped + prednisone 10-30mg per day
Day 61 - 120: Everolimus dose adjusted + cyclosporine adjust dose according protocol guideline (or commence reduction by day 120 at discretion of Investigator, to be completed within 2 months of commencement) + gradual withdrawal of prednisone by 1 mg/week to be discontinued by Day 120.
Day 121 - Month 36: At Day 121, Month 7 and Month 13 Everolimus dose was adjusted to achieve target 6-10 ng/mL + Cyclosporine adjust dose to achieve C2 target as per protocol Receives: Drug: Everolimus (RAD001); Drug: Cyclosporine (Calcineurin Inhibitor (CNI)); Drug: Methylprednisone/prednisone; Drug: Mycophenolate sodium (MPA) |
| CNI+MPA+ Steroid | Active comparator | Patients randomized to this group received:
Day 1 - Month 36: cyclosporine 5 mg/kg b.i.d., dose adjusted to achieve the protocol defined C2 Targets + mycophenolate sodium 720mg b.i.d. + Methylprednisone/prednisone 500mg intra-operatively, 250mg on day 1, 10-30mg prednisone per day until month 12 (as per local practice), 5-10mg/day months 13-36. Receives: Drug: Cyclosporine (Calcineurin Inhibitor (CNI)); Drug: Methylprednisone/prednisone; Drug: Mycophenolate sodium (MPA) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Calculated Glomerular Filtration Rate (cGFR) After Kidney Transplant to Evaluate Kidney Function (12 Months Analysis)
The glomerular filtration rate (GFR) was calculated by the Nankivell formula: GFR = 6.7 / Scr + BW / 4 - Surea / 2-100 / (height)^ 2 + C where Scr is the serum creatinine concentration expressed in mmol/L, BW the body weight in kg, Surea the serum urea in mmol/L, height in m, and the constant C is 35 for male and 25 for female patients.
Measured: At Month 12
Secondary outcomes (38)
Calculated Glomerular Filtration Rate (cGFR) After Kidney Transplant to Evaluate Kidney Function (36 Months Analysis)
The glomerular filtration rate (GFR) was calculated by the Nankivell formula: GFR = 6.7 / Scr + BW / 4 - Surea / 2-100 / (height)^ 2 + C where Scr is the serum creatinine concentration expressed in mmol/L, BW the body weight in kg, Surea the serum urea in mmol/L, height in m, and the constant C is 35 for male and 25 for female patients.
Measured: At Month 24 and 36
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Per Treatment Group (12 Months Analysis)
A biopsy-proven acute rejection is defined as a biopsy graded IA, IB, IIA, IIB, or III as per Banff 97 classification.
Measured: At Month 12
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Per Treatment Group (36 Months Analysis)
A biopsy-proven acute rejection is defined as a biopsy graded IA, IB, IIA, IIB, or III as per Banff 97 classification.
Measured: At Month 12, 24 and 36
Number of Participants With Composite Endpoint of Treatment Failure (12 Months Analysis)
Composite endpoint of treatment failure includes biopsy-proven acute rejection (BPAR), graft loss, death and loss-to-follow-up. A BPAR is defined as a biopsy graded IA, IB, IIA, IIB, or III as per Banff 97 classification.
The allograft was presumed to be lost on the day the patient started dialysis and was not able to subsequently be removed from dialysis. If the patient underwent a graft nephrectomy, then the day of nephrectomy was the day of graft loss.
Measured: Month 12
Number of Participants With Composite Endpoint of Treatment Failure (36 Months Analysis)
Composite endpoint of treatment failure includes biopsy-proven acute rejection (BPAR), graft loss, death and loss-to-follow-up. A BPAR is defined as a biopsy graded IA, IB, IIA, IIB, or III as per Banff 97 classification.
The allograft was presumed to be lost on the day the patient started dialysis and was not able to subsequently be removed from dialysis. If the patient underwent a graft nephrectomy, then the day of nephrectomy was the day of graft loss.
Measured: At Month 12, 24 and 36
Number of Participants With Histological Evidence Chronic Allograft Nephropathy (CAN) (12 Months Analysis)
A per-protocol biopsy was performed at Baseline and Month 12 and read by an independent blinded pathologist in order to assess chronic allograft nephropathy. Chronic rejection is characterized by a slow progressive decline in renal function and is typically preceded by the histological picture of chronic allograft nephropathy. The presence of biopsy confirmed Grade I, II or III chronic allograft nephropathy by Banff 97 criteria was assessed on all optional biopsies obtained for clinical suspicion of chronic rejection.
Data summarized by 3 categories. "Yes" - Patients with histological evidence of CAN ; "No" - Patients with histological evidence of CAN and "Not Done" - Central protocol defined kidney allograft biopsies were not done.
Measured: At Month 12
Number of Participants With Histological Evidence Chronic Allograft Nephropathy (CAN) (36 Months Analysis)
Chronic rejection is characterized by a slow progressive decline in renal function and is typically preceded by the histological picture of chronic allograft nephropathy. The presence of biopsy confirmed Grade I, II or III chronic allograft nephropathy by Banff 97 criteria was assessed on all optional biopsies obtained for clinical suspicion of chronic rejection.
Data summarized by 3 categories. "Yes" - Patients with histological evidence of CAN ; "No" - Patients with histological evidence of CAN and "Not Done" - Central protocol defined kidney allograft biopsies were not done.
Measured: At Month 36
Number of Participants With Sub Clinical Acute Rejection (12 Months Analysis)
Based on Banff 97 criteria, sub clinical acute rejection can be:
GRADE IA - Cases with significant interstitial infiltration (>25% of parenchyma affected) and foci of moderate tubulitis (>4 mononuclear cells/tubular cross section or group of 10 tubular cells).
GRADE IB - Cases with significant interstitial infiltration (>25% of parenchyma affected) and foci of moderate tubulitis (>10 mononuclear cells/tubular cross section or group of 10 tubular cells).
GRADE IIA - Cases with significant interstitial infiltration and mild to moderate intimal arteritis (v1).
GRADE IIB - Cases with moderate to severe intimal arteritis comprising >25% of the luminal area (v2).
GRADE III - Cases with "transmural" arteritis or fibrinoid change and necrosis of medial smooth muscle cells (v3).
"Borderline" category is used when no intimal arteritis is present, but there are foci of mild tubulitis (1 to 4 mononuclear cells/tubular cross section).
Measured: At Month 12
Number of Participants With Sub Clinical Acute Rejection (36 Months Analysis)
Based on Banff 97 criteria, sub clinical acute rejection can be:
GRADE IA - Cases with significant interstitial infiltration (>25% of parenchyma affected) and foci of moderate tubulitis (>4 mononuclear cells/tubular cross section or group of 10 tubular cells).
GRADE IB - Cases with significant interstitial infiltration (>25% of parenchyma affected) and foci of moderate tubulitis (>10 mononuclear cells/tubular cross section or group of 10 tubular cells).
GRADE IIA - Cases with significant interstitial infiltration and mild to moderate intimal arteritis (v1).
GRADE IIB - Cases with moderate to severe intimal arteritis comprising >25% of the luminal area (v2).
GRADE III - Cases with "transmural" arteritis or fibrinoid change and necrosis of medial smooth muscle cells (v3).
"Borderline' category is used when no intimal arteritis is present, but there are foci of mild tubulitis (1 to 4 mononuclear cells/tubular cross section).
Measured: At Month 36
Mean Serum Creatinine (12 Months Analysis)
Measured: At Month 12
Mean Serum Creatinine (36 Months Analysis)
Measured: At Month 12, 18, 24 and 36
Creatinine Clearance (CrCl) Calculated by the Cockcroft-Gault Formula (12 Months Analysis)
Creatinine clearance were calculated according to the Cockcroft-Gault formula:
CrCl (males) = (140-A) × BW/(72 × Cr) CrCl (females) = CrCl (males) × 0.85 where A is age [years], BW is body weight [kg], and Cr is the serum concentration of creatinine [mg/dL].
The Cockcroft-Gault formula estimates creatinine clearance based on serum creatinine level, body weight, and age.
Measured: At Month 12
Creatinine Clearance Calculated by the Cockcroft-Gault Formula (36 Months Analysis)
Creatinine clearance were calculated according to the Cockcroft-Gault formula:
CrCl (males) = (140-A) × BW/(72 × Cr) CrCl (females) = CrCl (males) × 0.85 where A is age [years], BW is body weight [kg], and Cr is the serum concentration of creatinine [mg/dL].
The Cockcroft-Gault formula estimates creatinine clearance based on serum creatinine level, body weight, and age.
Measured: At Month 12, 24 and 36
Mean Urine Albumin/Creatinine Ratio (ACR) as Measurement of Proteinuria (12 Months Analysis)
Proteinuria is measured by spot morning urine Albumin/Creatinine Ratio [ACR]. When the ACR is more than or equal to 30 mg/mmol then it is known as proteinuria.
Measured: At Month 12
Mean Urine Albumin/Creatinine Ratio [ACR] as Measurement of Proteinuria (36 Months Analysis)
Proteinuria is measured by spot morning urine Albumin/Creatinine Ratio [ACR]. When the ACR is more than or equal to 30 mg/mmol then it is known as proteinuria.
Measured: At Month 12, 18, 24 and 36
Number of Participants With Post Transplant Diabetes Mellitus (PTDM) and Impaired Fasting Glucose (12 Months Analysis)
The symptoms of post transplant diabetes mellitus (PTDM) and impaired fasting glucose are defined as any of the following conditions:
- Patients receiving glucose lowering treatment
- Fasting plasma glucose (FPG) >= 126 mg/dL on 2 separate occasions
- Hemoglobin subtype A1c (HbA1c) > 6.5%
- Diabetes reported as treatment emergent AE with end date > Day 15
Measured: At Month 12
Number of Participants With New Onset Diabetes Mellitus After Transplantation (NODAT) and Impaired Fasting Glucose (36 Months Analysis)
The symptoms of new onset diabetes mellitus after transplantation (NODAT) and impaired fasting glucose are defined as any of the following conditions:
- Patients receiving glucose lowering treatment
- 2 fasting plasma glucose (FPG) values >= 126 mg/dL or 2 random plasma glucose (RPG) values >= 200 mg/dL or FPG value >= 126 mg/dL and 1 RPG value >= 200 mg/dL
- Diabetes reported as treatment emergent AE with end date > Day 15
Measured: At Month 36
Number of Participants With Notable Abnormal Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) as Measurement of Effect of Treatment on Cardiovascular Health (12 Months Analysis)
Notable abnormal systolic blood pressure is defined as :
- Either an increase of >=30 that results in >=180 or >200 (mm/Hg)
- OR a decrease of >=30 that results in <=90 or <75 (mm/Hg)from baseline
Notable abnormal diastolic blood pressure is defined as :
- Either an increase of >=20 that results in >=105 or >115 (mm/Hg)
- OR a decrease of >=20 that results in <=50 or <40 (mm/Hg) from baseline
Measured: Baseline, Overall post-baseline up to 12 month
Number of Participants With Notable Abnormal Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) as Measurement of Effect of Treatment on Cardiovascular Health (36 Months Analysis)
Notable abnormal systolic blood pressure is defined as :
- Either an increase of >=30 that results in >=180 or >200 (mm/Hg)
- OR a decrease of >=30 that results in <=90 or <75 (mm/Hg) from baseline
Notable abnormal diastolic blood pressure is defined as :
- Either an increase of >=20 that results in >=105 or >115 (mm/Hg)
- OR a decrease of >=20 that results in <=50 or <40 (mm/Hg) from baseline
Measured: Baseline, Overall post baseline up to Month 36
Number of Participants With Erythropoietin Usage (12 Months Analysis)
Measured: Month 12
Number of Participants With Erythropoietin Usage (36 Months Analysis)
Measured: Month 36
Mean Short-form 36 Health Survey (SF-36) Score as a Measure of Quality of Life Assessment (12 Months Analysis)
SF-36 measures impact of disease on overall quality of life (QoL). 36-item survey has 8 subscales. The 8 subscales are: Physical functioning (PF), Role-physical (RP), Bodily pain (BP), General health (GH), Vitality (VT), Social functioning (SF), Role-emotional (RE) and Mental health (MH).
Score for eash sub-scale has been standardized with the use of norm-based methods based on assessment of the general U.S. population free of chronic conditions. Scores range from 1-100 with a mean=50 and a standard deviation=10. A higher score indicates less impact on QoL.
Measured: At Month 12
Mean Short-form 36 Health Survey (SF-36) Score as a Measure of Quality of Life Assessment (36 Months Analysis)
SF-36 measures impact of disease on overall quality of life (QoL). 36-item survey has 8 subscales. The 8 subscales are : Physical functioning (PF), Role-physical (RP), Bodily pain (BP), General health (GH), Vitality (VT), Social functioning (SF), Role-emotional (RE) and Mental health (MH).
Score for each sub-scale has been standardized with the use of norm-based methods based on assessment of the general U.S. population free of chronic conditions. Scores range from 1-100 with a mean=50 and a standard deviation=10. A higher score indicates less impact on QoL.
Measured: At Month 24
Number of Participants Hospitalized for Reasons Other Than Primary Transplantation (12 Months Analysis)
This analysis is reporting number of participants hospitalized for reasons (such as acute rejection, infection, gastrointestinal (GI) events, cardiovascular event, metabolic disorder and Other) other than primary transplantation.
Measured: Month 12
Number of Participants Hospitalized for Reasons Other Than Primary Transplantation (36 Months Analysis)
This analysis is reporting number of participants hospitalized for reasons (such as acute rejection, infection, gastrointestinal (GI) events, cardiovascular event, metabolic disorder and Other) other than primary transplantation.
Measured: Month 36
Number of Participants With Employment Status (12 Months Analysis)
The various employment status reported are:
- Employed/self employed full time
- Employed part time
- Unemployed
- Homemaker
- Volunteer
- Permanently disabled
- Non-permanently disable
- Retired
- Other
Measured: At screening (at day 0 +/- 7 days ), At Month 12
Number of Participants With Employment Status (36 Months Analysis)
The various employment status reported are:
- Employed/self employed full time
- Employed part time
- Unemployed
- Homemaker
- Volunteer
- Permanently disabled
- Non-permanently disable
- Retired
- Other
Measured: At screening (at day 0 +/- 7 days ), At Month 36
Number of Participants With Wound Problems(12 Months Analysis)
Patients with any wound healing problem such as infection related to kidney surgery, dehiscence, lymphocele, hernia, seroma, hematoma, ureteral anastomotic complication and other were reported in this analysis.
Measured: At Month 12
Number of Participants With Any Wound Problems (36 Months Analysis)
Patients with any wound healing problem such as infection related to kidney surgery, dehiscence, lymphocele, hernia, seroma, hematoma, ureteral anastomotic complication and other were reported in this analysis.
Measured: At Month 12, 24 and 36
Number of Participants With Notable Abnormalities in Total Cholesterol and Triglycerides as Measurement of Effect of Treatment on Cardiovascular Health (12 Months Analysis)
Notable abnormal total cholesterol is defined as : High: >= 9.1 mmol/L , normal range is 0.00 - 5.17 mmol/L
Notable abnormal triglycerides is defined as : High: >= 8.5 mmol/L, normal range is 0.30 - 2.00 mmol/L
Measured: Overall post baseline up to month 12
Number of Participants With Notable Abnormalities in Total Cholesterol and Triglycerides as Measurement of Effect of Treatment on Cardiovascular Health (36 Months Analysis)
Notable abnormal total cholesterol is defined as : High: >= 9.1 mmol/L , normal range is 0.00 - 5.17 mmol/L
Notable abnormal triglycerides is defined as : High: >= 8.5 mmol/L, normal range is 0.30 - 2.00 mmol/L
Measured: Overall Post Baseline up to month 36
Number of Participants With Antibody-mediated Rejection Per Treatment Group (12 Months Analysis)
Measured: At Month 12
Number of Participants With Antibody-mediated Rejection Per Treatment Group (36 Months Analysis)
Measured: At Month 12, 24 and 36
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Influenced by Demographic Characteristics and Morbidities (12 Months Analysis)
The influence of demographic characteristics and comorbidities on incidence of BPAR were analyzed in the following way: Demographic characteristics were age (<55 years, ≥55 years), Expanded criteria Donor (ECD) organ (donor age >60 years or donor non heart-beating and donor age >50), gender, living vs. deceased donor, Body Mass Index (BMI) classes (underweight <18.5, normal 18.5 - <25.0, overweight 25.0 - <30.0, obesity 30.0 and above), years on dialysis before transplantation (<1, 1-5, >5 years). Comorbidities were diabetes, hypertension, cardiovascular diseases/events, nephrosclerosis, glomerulonephritis/glomerular disease, polycystic disease, and Cytomegalovirus status.
Measured: At Month 12
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Influenced by Demographic Characteristics and Morbidities (36 Months Analysis)
The influence of demographic characteristics and comorbidities on incidence of BPAR were analyzed in the following way: Demographic characteristics were age (<55 years, ≥55 years), Expanded Criteria Donor [ECD] organ (donor age >60 years or donor non heart-beating and donor age >50), gender, living vs. deceased donor, Body Mass Index (BMI) classes (underweight <18.5, normal 18.5 - <25.0, overweight 25.0 - <30.0, obesity 30.0 and above), years on dialysis before transplantation (<1, 1-5, >5 years). Comorbidities were diabetes, hypertension, cardiovascular diseases/events, nephrosclerosis, glomerulonephritis/glomerular disease, polycystic disease, and Cytomegalovirus status.
Measured: At Month 36
Number of Patient Survival and Graft Survival (12 Months Analysis)
Measured: At Month 12
Number of Patient Survival and Graft Survival (36 Months Analysis)
Measured: At Month 12, 24 and 36
Change in Bone Mineral Density Between Week 2 and Month 24 (36 Months Analysis)
Measurements of bone mineral density (BMD) by Dual Energy X-ray Absorptiometry (DEXA) were done at Week 2 and Month 24. Change in BMD between week 2 and Month 24 were done for neck of femur and lumbar spine.
Measured: Week 2, Month 24
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Sep 2006 (estimated)
- Study startMar 2006
- Primary completionJun 2012
- Study completionJun 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Renal Transplanted RecipientsStudies of the same condition, open and under way.
- More trials run by Novartis PharmaceuticalsThe 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 126 participants (actual)
Sponsor and investigators
- Lead sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Novartis, Study director, Novartis
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00371826
- Sponsor's protocol ID
- CRAD001A2421
- Status last verified
- Jun 2013
- First submitted
- 1 Sep 2006
- Last updated
- 19 Aug 2013
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 19 Aug 2013. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective, Open-label, Controlled Multicenter Trial to Assess the Efficacy and Safety of an Induction Regimen of Cyclosporine Micro Emulsion, Enteric-coated Mycophenolate Sodium (EC-MPS) and Corticosteroids, Followed by Administration of Everolimus and Enteric-coated Mycophenolate Sodium (EC-MPS), With Either the Withdrawal of Cyclosporine Micro Emulsion or Corticosteroids in de Novo Kidney Transplant Recipients
- ClinicalTrials.gov ID
- NCT00371826
- Acronym / sponsor ID
- CRAD001A2421
- Conditions
- Renal Transplanted Recipients
- Keywords
- Renal transplantation, everolimus, Immunosuppressants
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 126 participants (actual)
- Lead sponsor
- Novartis PharmaceuticalsIndustry (pharma, biotech, devices)
- Study start
- Mar 2006
- Primary completion
- Jun 2012 (actual)
- Study completion
- Jun 2012 (actual)
- First posted
- 4 Sep 2006 (estimated)
- Results
- Posted 19 Aug 2013
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to assess the safety and efficacy of corticosteroid discontinuation versus cyclosporine micro emulsion discontinuation in recipients receiving reduced exposure cyclosporine micro emulsion and corticosteroids plus enteric-coated mycophenolate sodium (EC-MPS) initially, changed to everolimus at 2 weeks post-transplant. These two groups will be compared to a third control group, who will receive treatment consisting of cyclosporine micro emulsion, enteric-coated mycophenolate sodium (EC-MPS) and steroids.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Calcineurin Inhibitor (CNI) Withdrawal | Experimental | Drug: Everolimus (RAD001), Drug: Cyclosporine (Calcineurin Inhibitor (CNI)), Drug: Methylprednisone/prednisone, Drug: Mycophenolate sodium (MPA)Every randomized patient in this group received Day 1 - Day 14: cyclosporine as Calcineurin Inhibitor (CNI) 5 mg/kg twice daily (b.i.d.), dose adjusted to achieve C2 target of 1,500 ng/mL (range 1,400-1,600 ng/mL) + mycophenolate sodium (MPA)720 mg b.i.d. + methylprednisone/prednisone 500 mg intra-operatively, 250 mg on day 1, then 10-30 mg/day prednisone Day 15 - Day 60: everolimus 1.5 mg b.i.d. to achieve target 6-10 ng/mL + cyclosporine decrease dose as per protocol guideline + MPA 720 mg b.i.d. until everolimus trough >6 ng/mL, then MPA was stopped + prednisone 10-30mg/day Day 61 - Day 120: everolimus dose adjusted to achieve target 6-10 ng/mL + cyclosporine 25% dose reduction per fortnight, to be discontinued by day 120 as per protocol (or commence reduction by day 120 at discretion of investigator, to be completed within 2 months of commencement) + prednisone 10-30mg/day Day 121 - Month 36: everolimus dose adjusted to achieve target 8-12 ng/mL + prednisone 5-10 mg/day |
| Steroid Withdrawal | Experimental | Drug: Everolimus (RAD001), Drug: Cyclosporine (Calcineurin Inhibitor (CNI)), Drug: Methylprednisone/prednisone, Drug: Mycophenolate sodium (MPA)Every randomized patient in this group received Day 1 -14: cyclosporine 5 mg/kg b.i.d., dose adjusted to achieve C2 target as per protocol + mycophenolate sodium (MPA) 720 mg b.i.d. + methylprednisone/prednisone 500 mg intra-operatively, 250 mg on day 1, then 10-30 mg prednisone per day Day 15 - 60: everolimus 1.5 mg b.i.d. to achieve target 6-10 ng/mL + cyclosporine decrease dose as per protocol guideline + MPA 720 mg b.i.d. until everolimus trough >6 ng/mL, then MPA was stopped + prednisone 10-30mg per day Day 61 - 120: Everolimus dose adjusted + cyclosporine adjust dose according protocol guideline (or commence reduction by day 120 at discretion of Investigator, to be completed within 2 months of commencement) + gradual withdrawal of prednisone by 1 mg/week to be discontinued by Day 120. Day 121 - Month 36: At Day 121, Month 7 and Month 13 Everolimus dose was adjusted to achieve target 6-10 ng/mL + Cyclosporine adjust dose to achieve C2 target as per protocol |
| CNI+MPA+ Steroid | Active comparator | Drug: Cyclosporine (Calcineurin Inhibitor (CNI)), Drug: Methylprednisone/prednisone, Drug: Mycophenolate sodium (MPA)Patients randomized to this group received: Day 1 - Month 36: cyclosporine 5 mg/kg b.i.d., dose adjusted to achieve the protocol defined C2 Targets + mycophenolate sodium 720mg b.i.d. + Methylprednisone/prednisone 500mg intra-operatively, 250mg on day 1, 10-30mg prednisone per day until month 12 (as per local practice), 5-10mg/day months 13-36. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Males and females aged 18-65 years inclusive.
- First time recipients of cadaveric, living unrelated or living related donor kidney transplants.
- Patients who are willing and able to participate in the study and from whom written informed consent has been obtained.
Key exclusion criteria (5 listed)
- Patients who are recipients of multiple organ transplants, including more than one kidney, kidney and pancreas, or previous transplant with any organ other than kidney.
- Patients at high immunological risk of graft loss, indicated by peak PRA >50% or loss of a previous renal allograft within the first 6 months of transplantation due to acute rejection.
- Patients who have received an investigational drug within 4 weeks prior to the screening visit.
- Presence of any severe allergy or hypersensitivity to drugs similar to everolimus (e.g. antibiotics such as Clindamycin)
- Other protocol-defined inclusion/exclusion criteria may applied
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 |
|---|---|---|
| Everolimus (RAD001)Also: Certican® | Drug | Calcineurin Inhibitor (CNI) Withdrawal, Steroid Withdrawal |
| Cyclosporine (Calcineurin Inhibitor (CNI))Also: Neoral® | Drug | CNI+MPA+ Steroid, Calcineurin Inhibitor (CNI) Withdrawal, Steroid Withdrawal |
| Methylprednisone/prednisone | Drug | CNI+MPA+ Steroid, Calcineurin Inhibitor (CNI) Withdrawal, Steroid Withdrawal |
| Mycophenolate sodium (MPA)Also: myfortic® | Drug | CNI+MPA+ Steroid, Calcineurin Inhibitor (CNI) Withdrawal, Steroid Withdrawal |
Primary outcome
Calculated Glomerular Filtration Rate (cGFR) After Kidney Transplant to Evaluate Kidney Function (12 Months Analysis)
Time frame: At Month 12
The glomerular filtration rate (GFR) was calculated by the Nankivell formula: GFR = 6.7 / Scr + BW / 4 - Surea / 2-100 / (height)^ 2 + C where Scr is the serum creatinine concentration expressed in mmol/L, BW the body weight in kg, Surea the serum urea in mmol/L, height in m, and the constant C is 35 for male and 25 for female patients.
38 secondary outcomes
Calculated Glomerular Filtration Rate (cGFR) After Kidney Transplant to Evaluate Kidney Function (36 Months Analysis)
Time frame: At Month 24 and 36
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Per Treatment Group (12 Months Analysis)
Time frame: At Month 12
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Per Treatment Group (36 Months Analysis)
Time frame: At Month 12, 24 and 36
Number of Participants With Composite Endpoint of Treatment Failure (12 Months Analysis)
Time frame: Month 12
Number of Participants With Composite Endpoint of Treatment Failure (36 Months Analysis)
Time frame: At Month 12, 24 and 36
Number of Participants With Histological Evidence Chronic Allograft Nephropathy (CAN) (12 Months Analysis)
Time frame: At Month 12
Number of Participants With Histological Evidence Chronic Allograft Nephropathy (CAN) (36 Months Analysis)
Time frame: At Month 36
Number of Participants With Sub Clinical Acute Rejection (12 Months Analysis)
Time frame: At Month 12
Number of Participants With Sub Clinical Acute Rejection (36 Months Analysis)
Time frame: At Month 36
Mean Serum Creatinine (12 Months Analysis)
Time frame: At Month 12
Mean Serum Creatinine (36 Months Analysis)
Time frame: At Month 12, 18, 24 and 36
Creatinine Clearance (CrCl) Calculated by the Cockcroft-Gault Formula (12 Months Analysis)
Time frame: At Month 12
Creatinine Clearance Calculated by the Cockcroft-Gault Formula (36 Months Analysis)
Time frame: At Month 12, 24 and 36
Mean Urine Albumin/Creatinine Ratio (ACR) as Measurement of Proteinuria (12 Months Analysis)
Time frame: At Month 12
Mean Urine Albumin/Creatinine Ratio [ACR] as Measurement of Proteinuria (36 Months Analysis)
Time frame: At Month 12, 18, 24 and 36
Number of Participants With Post Transplant Diabetes Mellitus (PTDM) and Impaired Fasting Glucose (12 Months Analysis)
Time frame: At Month 12
Number of Participants With New Onset Diabetes Mellitus After Transplantation (NODAT) and Impaired Fasting Glucose (36 Months Analysis)
Time frame: At Month 36
Number of Participants With Notable Abnormal Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) as Measurement of Effect of Treatment on Cardiovascular Health (12 Months Analysis)
Time frame: Baseline, Overall post-baseline up to 12 month
Number of Participants With Notable Abnormal Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) as Measurement of Effect of Treatment on Cardiovascular Health (36 Months Analysis)
Time frame: Baseline, Overall post baseline up to Month 36
Number of Participants With Erythropoietin Usage (12 Months Analysis)
Time frame: Month 12
Number of Participants With Erythropoietin Usage (36 Months Analysis)
Time frame: Month 36
Mean Short-form 36 Health Survey (SF-36) Score as a Measure of Quality of Life Assessment (12 Months Analysis)
Time frame: At Month 12
Mean Short-form 36 Health Survey (SF-36) Score as a Measure of Quality of Life Assessment (36 Months Analysis)
Time frame: At Month 24
Number of Participants Hospitalized for Reasons Other Than Primary Transplantation (12 Months Analysis)
Time frame: Month 12
Number of Participants Hospitalized for Reasons Other Than Primary Transplantation (36 Months Analysis)
Time frame: Month 36
Number of Participants With Employment Status (12 Months Analysis)
Time frame: At screening (at day 0 +/- 7 days ), At Month 12
Number of Participants With Employment Status (36 Months Analysis)
Time frame: At screening (at day 0 +/- 7 days ), At Month 36
Number of Participants With Wound Problems(12 Months Analysis)
Time frame: At Month 12
Number of Participants With Any Wound Problems (36 Months Analysis)
Time frame: At Month 12, 24 and 36
Number of Participants With Notable Abnormalities in Total Cholesterol and Triglycerides as Measurement of Effect of Treatment on Cardiovascular Health (12 Months Analysis)
Time frame: Overall post baseline up to month 12
Number of Participants With Notable Abnormalities in Total Cholesterol and Triglycerides as Measurement of Effect of Treatment on Cardiovascular Health (36 Months Analysis)
Time frame: Overall Post Baseline up to month 36
Number of Participants With Antibody-mediated Rejection Per Treatment Group (12 Months Analysis)
Time frame: At Month 12
Number of Participants With Antibody-mediated Rejection Per Treatment Group (36 Months Analysis)
Time frame: At Month 12, 24 and 36
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Influenced by Demographic Characteristics and Morbidities (12 Months Analysis)
Time frame: At Month 12
Number of Participants With Biopsy Proven Acute Rejection (BPAR) Influenced by Demographic Characteristics and Morbidities (36 Months Analysis)
Time frame: At Month 36
Number of Patient Survival and Graft Survival (12 Months Analysis)
Time frame: At Month 12
Number of Patient Survival and Graft Survival (36 Months Analysis)
Time frame: At Month 12, 24 and 36
Change in Bone Mineral Density Between Week 2 and Month 24 (36 Months Analysis)
Time frame: Week 2, Month 24
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Aug 2013.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
Related trials for Renal Transplanted Recipients
RecruitingPhase 2
A Study of Mezagitamab in Adults With Late Antibody-Mediated Rejection (AMR) After a Kidney Transplant
Antibody-Mediated Rejection (AMR)
Not yet recruitingEarly Phase 1
Biomarker-Guided Mycophenolate Mofetil Elimination in Low-Risk Older Adult Kidney Transplant Recipients
Kidney Transplant Recipient
Recruiting
Non-Invasive Monitoring of Pediatric Kidney Transplant Recipients and Immunosuppression Personalization: an Open-labeled Multicenter Randomized Controlled Study
Pediatric Kidney Disease, Transplant;Failure,Kidney
Not yet recruitingPhase 2
(TNX-1500) in Kidney Transplant Recipients
Kidney Transplant, Kidney Transplant Failure and Rejection
Active, not recruitingPhase 1/2
Carfilzomib and Belatacept for Desensitization
Highly Sensitized Prospective Kidney Transplant Recipients
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.
Novartis study director
Novartis
7 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Everolimus (RAD001), Cyclosporine (Calcineurin Inhibitor (CNI)) and Methylprednisone/prednisone in people with Renal Transplanted Recipients, run by Novartis Pharmaceuticals at 7 sites in Australia.
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 3 inclusion and 5 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 19 Aug 2013. 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 Australia. 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 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 19 Aug 2013). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
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?
Calculated Glomerular Filtration Rate (cGFR) After Kidney Transplant to Evaluate Kidney Function (12 Months Analysis) (time frame: At Month 12). 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 19 Aug 2013.