Your session is about to expire
← Back to Search
SGLT2 Inhibitor
Dapagliflozin for Kidney Amyloidosis (FLORAL Trial)
Phase 2
Waitlist Available
Led By Jeffery Zonder, M.D.
Research Sponsored by Jeffrey Zonder
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age ≥18 years
Plateau in any renal response (i.e., reduction in proteinuria) for at least 3 months prior to enrollment, as determined by the enrolling physician
Must not have
Baseline eGFR <25 mL/min/1.73m2
Current or previous use of any SGLT2i
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to month 6
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to test if a pill called dapagliflozin is safe and effective in reducing high protein levels in the urine of patients with renal AL amyloidosis. Participants will be screened
Who is the study for?
This trial is for patients with renal AL amyloidosis, a condition where abnormal proteins build up in the kidneys. Participants must be comfortable using online platforms and telemedicine for screening, consent, instructions, medication delivery, and follow-ups.
What is being tested?
The FLORAL study is testing if dapagliflozin taken orally can lower protein levels in urine of renal AL amyloidosis patients. The trial involves remote monitoring over six months with lab work and side effect assessments at set intervals.
What are the potential side effects?
Potential side effects of dapagliflozin include dehydration, low blood pressure, kidney problems, high cholesterol levels, yeast infections and urinary tract infections. Side effects will be monitored via telemedicine.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
My kidney condition has not improved for at least 3 months.
Select...
I can care for myself and am up and about more than 50% of my waking hours.
Select...
My kidney disease was confirmed by a biopsy and I have significant protein in my urine.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My kidney function is very low.
Select...
I have used SGLT2 inhibitors for my diabetes.
Select...
I do not have any active cancer needing treatment, except for AL amyloidosis or non-melanoma skin cancers.
Select...
I am being treated for diabetes.
Select...
I have or had symptoms of multiple myeloma, such as bone damage or high calcium levels.
Select...
I do not have severe liver problems like fluid buildup, bleeding veins in my esophagus, or blood clotting issues.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to month 6
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to month 6
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Proportion of patients achieving 30% reduction in daily proteinuria.
Secondary study objectives
Completion rate of tele-visits
Other study objectives
Incidence rate of developing dialysis dependent ESRD in patients with Pavia Renal AL Stage II or III involvement.
Proportion of patients experiencing any of the following: (1) sustained decline in eGFR, (2) onset of ESRD, or (3) death from a renal disease-related or cardiovascular cause.
Side effects data
From 2018 Phase 4 trial • 30 Patients • NCT0300647120%
Cervicovaginal infection
13%
Urinary tract infections
100%
80%
60%
40%
20%
0%
Study treatment Arm
Dapagliflozin
Placebo
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: DapagliflozinExperimental Treatment1 Intervention
Dapagliflozin 10mg orally, daily for 6 months
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Dapagliflozin
2014
Completed Phase 4
~64440
Find a Location
Who is running the clinical trial?
Jeffrey ZonderLead Sponsor
Jeffery Zonder, M.D.Principal InvestigatorBarbara Ann Karmanos Cancer Institute
1 Previous Clinical Trials
60 Total Patients Enrolled
Share this study with friends
Copy Link
Messenger