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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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

Other trials in Australia

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.

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 groups in NCT00371826
Study groupRoleWhat they receive
Calcineurin Inhibitor (CNI) WithdrawalExperimentalEvery 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 WithdrawalExperimentalEvery 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+ SteroidActive comparatorPatients 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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. Mean Serum Creatinine (12 Months Analysis)

    Measured: At Month 12

  11. Mean Serum Creatinine (36 Months Analysis)

    Measured: At Month 12, 18, 24 and 36

  12. 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

  13. 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

  14. 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

  15. 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

  16. 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:

    1. Patients receiving glucose lowering treatment
    2. Fasting plasma glucose (FPG) >= 126 mg/dL on 2 separate occasions
    3. Hemoglobin subtype A1c (HbA1c) > 6.5%
    4. Diabetes reported as treatment emergent AE with end date > Day 15

    Measured: At Month 12

  17. 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:

    1. Patients receiving glucose lowering treatment
    2. 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
    3. Diabetes reported as treatment emergent AE with end date > Day 15

    Measured: At Month 36

  18. 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

  19. 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

  20. Number of Participants With Erythropoietin Usage (12 Months Analysis)

    Measured: Month 12

  21. Number of Participants With Erythropoietin Usage (36 Months Analysis)

    Measured: Month 36

  22. 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

  23. 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

  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

  25. 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

  26. 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

  27. 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

  28. 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

  29. 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

  30. 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

  31. 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

  32. Number of Participants With Antibody-mediated Rejection Per Treatment Group (12 Months Analysis)

    Measured: At Month 12

  33. Number of Participants With Antibody-mediated Rejection Per Treatment Group (36 Months Analysis)

    Measured: At Month 12, 24 and 36

  34. 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

  35. 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

  36. Number of Patient Survival and Graft Survival (12 Months Analysis)

    Measured: At Month 12

  37. Number of Patient Survival and Graft Survival (36 Months Analysis)

    Measured: At Month 12, 24 and 36

  38. 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.

  1. First posted4 Sep 2006 (estimated)
  2. Study startMar 2006
  3. Primary completionJun 2012
  4. Study completionJun 2012

Resources

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)
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
Data monitoring committee
Yes

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.

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