Treating to Reduce Albuminuria and Normalize Hemodynamic Function in Focal ScLerosis With dApagliflozin Trial Effects (TRANSLATE)
Treating to Reduce Albuminuria and Normalize Hemodynamic Function in Focal ScLerosis With dApagliflozin Trial Effects: "The TRANSLATE Study"
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 4
Contacts and Locations
Study Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M5G 2N2
- Renal Physiology Laboratory, University Health Network
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Male or female subjects diagnosed with FSGS ≥1 month prior to informed consent
- eGFR≥45 ml/min/1.73m2
- Age 18 years or greater
- No history of diabetes
- Body Mass Index (BMI) 18.5 - 45.0 kg/ m2
- Blood pressure ≥ 100/60 at screening
- Stable therapy with either an ACEi or angiotensin II receptor blocker or direct renin inhibitor for > 1 month
- >30 mg/day and <6 g/day of proteinuria unless the patient is not a candidate for immunosuppressive therapy
Exclusion Criteria:
- Leukocyte and/or nitrite positive urinalysis that is untreated;
- History of organ transplantation, cancer, liver disease;
- Bariatric surgery or other gastrointestinal surgeries that induce chronic malabsorption within the past two years;
- Current treatment with systemic corticosteroids, calcineurin inhibitors, or other immunosuppressant medications;
- Blood dyscrasias or any disorders causing hemolysis or unstable red blood cells;
- Pre-menopausal women who are nursing, pregnant, or of child-bearing potential and not practising an acceptable method of birth control;
- Participation in another therapeutic trial with an investigational drug within 30 days prior to informed consent;
- Alcohol or drug abuse within three months prior to informed consent that would interfere with trial participation or any ongoing clinical condition that would jeopardize subject safety or study compliance based on investigator judgement;
- Liver disease, defined by serum levels of alanine transaminase, aspartate transaminase, or alkaline phosphatase >3 x upper limit of normal as determined during screening;
- Cardiac, lung or peripheral vascular disease or stroke;
- Pancreas, pancreatic islet cells or renal transplant recipient;
- Medical history of cancer or treatment for cancer in the last five years prior to screening;
- History of allergy or angioedema with RAAS inhibitor exposure;
- Kidney disease due primarily to another condition aside from FSGS;
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Dapagliflozin (trade name Farxiga®)
Oral tablet, 10mg, PO, 8 weeks
|
Oral tablet, 10mg, PO, 8 weeks
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The change in Glomerular Filtration Rate (GFR) After an 8 week treatment with dapagliflozin
Time Frame: Before and after an 8 week treatment with dapagliflozin
|
Glomerular Filtration Rate (GFR, based on plasma inulin clearance) will be measured at baseline and after 8 weeks of treatment.
|
Before and after an 8 week treatment with dapagliflozin
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The change in Effective Renal Plasma Flow (ERPF) After an 8 week treatment with dapagliflozin
Time Frame: Before and after an 8 week treatment with dapagliflozin
|
Effective Renal Plasma Flow (ERPF, based on paraaminohippurate plasma clearance) will be measured at baseline and after 8 weeks of treatment.
|
Before and after an 8 week treatment with dapagliflozin
|
|
The change in Blood Pressure After an 8 week treatment with dapagliflozin
Time Frame: Before and after 8 weeks of treatment with dapagliflozin
|
Before and after 8 weeks of treatment with dapagliflozin
|
|
|
The change in albuminuria after 8 weeks of treatment with dapagliflozin
Time Frame: Before and after 8 weeks of treatment with dapagliflozin
|
Before and after 8 weeks of treatment with dapagliflozin
|
|
|
The change in urinary vasoactive mediators after 8 weeks of treatment with dapagliflozin
Time Frame: Before and after 8 weeks of treatment with dapagliflozin
|
Before and after 8 weeks of treatment with dapagliflozin
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Kidney Diseases
- Urologic Diseases
- Urological Manifestations
- Urination Disorders
- Proteinuria
- Nephritis
- Glomerulonephritis
- Albuminuria
- Glomerulosclerosis, Focal Segmental
- Hypoglycemic Agents
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Sodium-Glucose Transporter 2 Inhibitors
- Dapagliflozin
Other Study ID Numbers
Other Study ID Numbers
- REB# 14-8284-B
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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