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CompletedNCT01649609Updated Feb 28, 2018Results posted

Using mTOR Inhibitors in the Prevention of BK Nephropathy

An interventional study of Tacrolimus and Mycophenolate acid in BK Viremia and BK Nephropathy, sponsored by Columbia University. Completed at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-02-28.

Sponsored by Columbia University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

BK virus infections after kidney transplant are increasing and can result in damage to the transplanted kidney. Currently, the universally accepted treatment is to decrease the strength of the antirejection medications but it is unclear what medications should be lowered and to what extent. The investigators propose to perform a study with patients who have BK virus detected in their blood during routine screening that appears to be increasing. The investigators will use two different strategies that involve different combinations of standard anti-rejection medications at lower dosages. Patients will be assigned to one of the two groups in a random manner across the two hospitals participating in the study. Patients will be followed for at least a year to determine if one strategy was more effective than the other in preventing an increase in the number of viruses in the blood stream and whether either one was more effective in reducing the negative impact of the infection on the functioning of the transplanted kidney.

Read the detailed description

The incidence of BK viremia, an early complication after renal transplantation and the associated rates of graft loss resulting from BK nephropathy have been steadily rising since a series of cases that were reported in the mid-1990's. While this is at least partly related to the introduction of newer immunosuppressive agents, recent United Network for Organ Sharing (UNOS) data analyses suggest that there is a continuing rise in the incidence of BK viremia and associated nephropathy with a 3.5% incidence rate in 2009 representing a dramatic rise from just 0.9% only 4 years earlier. Single center data reports have suggested much lower rates of BK viremia and nephropathy in cohorts treated with mTOR (mammalian target of rapamycin) based immunosuppressive regimens when compared to the overall national incidence rates. Recent data has demonstrated that calcineurin inhibitors at concentrations routinely used in clinical practice interfere with the BK virus specific T cell responses; an interference that is not seen to occur with mTOR inhibitors. Further, recent evidence that inhibition of the mTOR pathway has a direct and consequential negative impact on BK infected cells provides additional insight into the observed benefit associated with mTOR inhibitors. The growing problem of BK viremia among renal transplant patients is further compounded by the absence of effective management strategies that have been tested in a rigorous or controlled setting - a fact that was highlighted in a recent systematic review. The cornerstone for management so far has been the reduction of immunosuppression, largely based on the outcome of a single center study of screening patients for viremia and following with preemptive lowering of immunosuppression. Conversion from calcineurin inhibitors to mTOR inhibitors has been reported in small case series to be an effective measure that appears to be superior to merely lowering immunosuppression; however, this approach has not been tested with a robust clinical study design.

Currently, the diagnosis of BK nephropathy requires a renal biopsy, an invasive procedure with its own risks. In addition, identification of patients with viremia who progress to nephropathy and subsequent graft failure i.e. prognostication does not appear possible with the renal biopsy results at present. Validation of potential non-invasive biomarkers provides a unique opportunity for both detection and risk stratification of patients with BK viremia subsequent failure, which could lead to more informed therapeutic interventions while supporting the development of newer therapies.

02

Conditions studied

  • BK Viremia
  • BK Nephropathy

Keywords

  • BK Viremia
  • BK Nephropathy
  • mTOR inhibitor
  • renal transplant
03

In context

Viremia

82 studies on the registry are indexed under Viremia; 11 are open to participants now.

This study's enrollment of 40 is below the median of 58 across 59 interventional studies indexed under Viremia.

Browse Viremia studies →

Lead sponsor

Columbia University is the lead sponsor of 1,103 studies on the registry; 193 are open to participants now.

Of its 172 completed or terminated interventional studies of FDA-regulated products, 142 (83%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Renal transplant recipients age 18 years or over

Exclusion criteria

Exclusion Criteria:

  • Patients with multiorgan transplants
  • Patients on immunosuppressive regimens that include steroids or Sirolimus at the time of detection of viremia
  • ABO incompatible renal transplants
  • Three or more previous renal transplants
  • Patients with contraindications to tacrolimus, sirolimus, mycophenolate mofetil or mycophenolic acid.
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (actual)

Study arms

  • Active comparator
    Reduction of standard immunosuppression

    Low dose Tacrolimus with low dose Mycophenolate acid

    Drug: Tacrolimus · Drug: Mycophenolate acid

  • Active comparator
    mTOR Arm

    Low dose Sirolimus with low dose Mycophenolate acid (mTOR Substitution)

    Drug: Mycophenolate acid · Drug: Sirolimus

Interventions

  • DrugTacrolimus

    Reduction of standard immunosuppression - The standard of care immunosuppression treatment commonly used for renal transplant patients

    Also known as: Prograf

  • DrugMycophenolate acid

    Myfortic or CellCept - The standard of care immunosuppression treatment most commonly used for renal transplant patients

    Also known as: mycophenolate antimetabolite

  • DrugSirolimus

    mTOR Substitution - Replacing tacrolimus (a calcineurin inhibitor) with sirolimus (an mTOR inhibitor) along with reduction of mycophenolic acid

    Also known as: Rapamune

06

What researchers measure

Primary outcomes

  1. Number of Participants With BK Viral Load <600 Copies/mL

    A Viral load of \<600 copies/mL for at least 3 months indicates sustained clearance of BK viremia, confirmed by blood test

    Time frame: Up to 12 months from enrollment

Secondary outcomes

  1. Number of Participants With Incidence of BK Nephropathy

    The number of people with incidence of BK Nephropathy in each of the two Arms

    Time frame: Up to 24 months from randomization

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Results

Posted Feb 28, 2018

Participant flow

Participant flow — Overall Study
MilestoneStandard Immunosuppression Reduction ArmmTOR Substitution Arm
Started2020
Completed2020
Not completed00

Outcome measures

PrimaryNumber of Participants With BK Viral Load <600 Copies/mL

A Viral load of \<600 copies/mL for at least 3 months indicates sustained clearance of BK viremia, confirmed by blood test

Time frame:
Up to 12 months from enrollment
Reported as:
Count of participants · Participants
Number of Participants With BK Viral Load <600 Copies/mL
ParticipantsStandard Immunosuppression Reduction ArmmTOR Substitution Arm
Number of Participants With BK Viral Load <600 Copies/mL1317
SecondaryNumber of Participants With Incidence of BK Nephropathy

The number of people with incidence of BK Nephropathy in each of the two Arms

Time frame:
Up to 24 months from randomization
Reported as:
Count of participants · Participants
Number of Participants With Incidence of BK Nephropathy
ParticipantsStandard Immunosuppression Reduction ArmmTOR Substitution Arm
Number of Participants With Incidence of BK Nephropathy31

Adverse events

Collected over Up to 24 months. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Standard Immunosuppression Reduction Arm0/20 (0%)1/20 (5%)0/20 (0%)
mTOR Substitution Arm0/20 (0%)1/20 (5%)0/20 (0%)
Most frequent serious events
Most frequent serious events
EventStandard Immunosuppression Reduction ArmmTOR Substitution Arm
ProteinuriaRenal and urinary disorders1/200/20
Rapa PneumonitisRespiratory, thoracic and mediastinal disorders0/201/20

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Standard Immunosuppression Reduction ArmmTOR Substitution ArmTotal
<=18 years000
Between 18 and 65 years101828
>=65 years10212
Age, Continuous
Age, Continuous(Years)Standard Immunosuppression Reduction ArmmTOR Substitution ArmTotal
Mean61.04 ± 14.1252.39 ± 12.6956.7 ± 13.76
Sex: Female, Male
Sex: Female, Male(Participants)Standard Immunosuppression Reduction ArmmTOR Substitution ArmTotal
Female6814
Male141226
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Standard Immunosuppression Reduction ArmmTOR Substitution ArmTotal
Hispanic or Latino415
Not Hispanic or Latino151833
Unknown or Not Reported112
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Standard Immunosuppression Reduction ArmmTOR Substitution ArmTotal
American Indian or Alaska Native101
Asian448
Native Hawaiian or Other Pacific Islander011
Black or African American369
White10818
More than one race000
Unknown or Not Reported213
Region of Enrollment
Region of Enrollment(participants)Standard Immunosuppression Reduction ArmmTOR Substitution ArmTotal
United States202040
Delayed Graft Function
Delayed Graft Function(Participants)Standard Immunosuppression Reduction ArmmTOR Substitution ArmTotal
Count of participants8816
08

Study locations

2 sites
  • Columbia University Medical Center
    New York, New York 10032, United States
  • Weill Cornell Medical Center
    New York, New York 10065, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 28, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01649609
Lead sponsor
Columbia University
Collaborators
Pfizer, Cornell University
Responsible party
Sumit Mohan, MD (Assistant Professor of Clinical Medicine, Columbia University) — Principal investigator
First posted
Jul 25, 2012
Start date
Mar 2012
Primary completion
Dec 2016
Completion
Dec 2016
Results posted
Feb 28, 2018
Last update
Feb 28, 2018

Study contacts

Sumit Mohan, MD
principal investigator · Columbia University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2018. You cannot join it, but the record below documents what was studied.

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