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Tacrolimus Versus Prednisolone for the Treatment of Minimal Change Disease (MinTAC)

Primary Purpose

Minimal Change Disease

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
tacrolimus
prednisolone
Sponsored by
Imperial College Healthcare NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Minimal Change Disease focused on measuring nephrotic minimal change tacrolimus prednisolone

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with nephrotic syndrome (hypoalbuminaemia and protein creatinine ratio (PCR) > 100units), secondary to minimal change disease.
  • Age over 18.

Exclusion Criteria:

  • Hepatitis B, hepatitis C or HIV infection.
  • Untreated infection.
  • Females who are pregnant, breast feeding, or at risk of pregnancy and not using a medically acceptable form of contraception.
  • Patients who have been treated with immunosuppression over the last 18 months.
  • Patients who have had more than 3 relapses of nephrotic syndrome within 5 years.
  • Any condition judged by the investigator that would cause the study to be detrimental to the patient.

Sites / Locations

  • Hammersmith Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

prednisolone

tacrolimus

Arm Description

prednisolone tablets

tacrolimus tablets

Outcomes

Primary Outcome Measures

Percentage of Participants Achieving Complete Remission From Nephrotic Syndrome at 8 Weeks
normalisation of serum albumin and urine PCR <50 units

Secondary Outcome Measures

Percentage of Patients Achieving Complete Remission From Nephrotic Syndrome at 16 and 26 Weeks
Percentage of Patients Achieving Remission Who Then Relapse
Number of Serious Adverse Events
Change in Baseline Glomerular Filtration Rate

Full Information

First Posted
September 21, 2009
Last Updated
April 9, 2021
Sponsor
Imperial College Healthcare NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT00982072
Brief Title
Tacrolimus Versus Prednisolone for the Treatment of Minimal Change Disease
Acronym
MinTAC
Official Title
Tacrolimus vs Prednisolone for the Treatment Minimal Change Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
December 2009 (Actual)
Primary Completion Date
October 10, 2019 (Actual)
Study Completion Date
October 10, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College Healthcare NHS Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the effectiveness of tacrolimus (prograf) versus prednisolone for the treatment of nephrotic syndrome secondary to minimal change disease.
Detailed Description
Minimal change disease is a common cause of nephrotic syndrome in adults. Standard treatment is with high dose steroids which is often effective in controlling the nephrotic syndrome but has a high morbidity due to the side effects of the steroids. There is also a high relapse rate,therefore many patients require long term steroid therapy to control their disease which has significant morbidity and mortality. Some patients are or also become steroid resistant. There are studies showing the effectiveness of alkylating agents such as cyclophosphamide but the use of these drugs is limited by their toxicity, including increased rates of infection, cancers and infertility. Tacrolimus (prograf) is a T-cell specific calcineurin inhibitor that shares similar immunosuppressive actions with cyclosporine A.In other glomerular diseases such as focal segmental glomerulosclerosis and membranous glomerulonephritis, prograf has been shown to be a very effective treatment for proteinuria. This may be due to the immunomodulatory effects on the underlying disease, but there may also be a direct effect of tacrolimus (prograf) on the podocyte, stabilising the actin cytoskeleton and therefore decreasing protein leak.Therefore tacrolimus (prograf) is likely to be effective in reducing proteinuria in minimal change disease.It has also been shown to have a good side effect profile when used to allow the avoidance of steroids in transplantation.This study aims to prospectively study if tacrolimus (prograf) is effective as treatment for minimal change disease compared with standard therapy with steroids, and whether it has advantages in terms of side effect profile and prevention of relapse.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Minimal Change Disease
Keywords
nephrotic minimal change tacrolimus prednisolone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
prednisolone
Arm Type
Active Comparator
Arm Description
prednisolone tablets
Arm Title
tacrolimus
Arm Type
Experimental
Arm Description
tacrolimus tablets
Intervention Type
Drug
Intervention Name(s)
tacrolimus
Other Intervention Name(s)
prograff
Intervention Description
tacrolimus0.05mg/kg bd (levels 6-12ng/ml)
Intervention Type
Drug
Intervention Name(s)
prednisolone
Intervention Description
Prednisolone 1mg/kg maximum 60mg od
Primary Outcome Measure Information:
Title
Percentage of Participants Achieving Complete Remission From Nephrotic Syndrome at 8 Weeks
Description
normalisation of serum albumin and urine PCR <50 units
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Percentage of Patients Achieving Complete Remission From Nephrotic Syndrome at 16 and 26 Weeks
Time Frame
16 and 26 weeks
Title
Percentage of Patients Achieving Remission Who Then Relapse
Time Frame
2 years
Title
Number of Serious Adverse Events
Time Frame
3 years
Title
Change in Baseline Glomerular Filtration Rate
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with nephrotic syndrome (hypoalbuminaemia and protein creatinine ratio (PCR) > 100units), secondary to minimal change disease. Age over 18. Exclusion Criteria: Hepatitis B, hepatitis C or HIV infection. Untreated infection. Females who are pregnant, breast feeding, or at risk of pregnancy and not using a medically acceptable form of contraception. Patients who have been treated with immunosuppression over the last 18 months. Patients who have had more than 3 relapses of nephrotic syndrome within 5 years. Any condition judged by the investigator that would cause the study to be detrimental to the patient.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Megan Griffith, MBChBPhDFRCP
Organizational Affiliation
Imperial College NHS Trust
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Tom Cairns, MBBSMRCP
Organizational Affiliation
Imperial College NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hammersmith Hospital
City
London
ZIP/Postal Code
W12 OHS
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35230699
Citation
Azukaitis K, Palmer SC, Strippoli GF, Hodson EM. Interventions for minimal change disease in adults with nephrotic syndrome. Cochrane Database Syst Rev. 2022 Mar 1;3(3):CD001537. doi: 10.1002/14651858.CD001537.pub5.
Results Reference
derived

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Tacrolimus Versus Prednisolone for the Treatment of Minimal Change Disease

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