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SGLT-2 Inhibitor
SGLT-2 Inhibitor for Cystinuria
Phase 2
Waitlist Available
Led By Marshall Stoller, MD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
history of previous cystine kidney stones
History of previous cystine kidney stones
Must not have
Unable to give informed consent
Prior diagnosis of diabetes mellitus (type I or type II)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year and 3 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests whether taking dapagliflozin daily can help people with cystinuria, a genetic kidney disorder that causes painful kidney stones. Dapagliflozin increases sugar levels in the urine, which may help stop or break down the stones. The study will monitor patients to see if this treatment works.
Who is the study for?
This trial is for adults over 18 with a history of cystine kidney stones and confirmed cystinuria. Participants must be able to consent and not have diabetes, be pregnant or likely to become so without birth control, seriously ill, non-English speaking, incarcerated, or unable to give informed consent.
What is being tested?
The trial tests if Dapagliflozin, an FDA-approved drug for diabetes and heart failure that increases urine glucose levels can prevent or dissolve cystine stones in the kidneys by introducing enough glucose into the urine.
What are the potential side effects?
While not specified here, common side effects of SGLT-2 inhibitors like Dapagliflozin include yeast infections due to sugar in the urine, urinary tract infections (UTIs), increased urination and risk of dehydration.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have had cystine kidney stones in the past.
Select...
I have had cystine kidney stones in the past.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am unable to understand and agree to the study's procedures and risks.
Select...
I have been diagnosed with diabetes (type I or II).
Select...
My primary language is not English.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year and 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year and 3 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in cystine stone size over time (1 year and 3 months)
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: Study DrugExperimental Treatment1 Intervention
The study drug is Dapagliflozin
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Dapagliflozin
2014
Completed Phase 4
~64440
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Cystinuria is treated by preventing the formation of cystine stones in the kidneys. One common approach is to break or prevent the cystine bond at the molecular level, making it less likely to precipitate in the urine.
SGLT-2 inhibitors, which are being studied for this purpose, work by increasing the concentration of glucose in the urine. This increased glucose may help prevent or reverse the formation of cystine stones by interfering with cystine's ability to form crystals.
This mechanism is crucial for cystinuria patients as it offers a potential non-invasive treatment option to manage and reduce the recurrence of painful kidney stones.
Treatment of clinically normal and cystinuric dogs with 2-mercaptopropionylglycine.
Treatment of clinically normal and cystinuric dogs with 2-mercaptopropionylglycine.
Find a Location
Who is running the clinical trial?
University of California, San FranciscoLead Sponsor
2,580 Previous Clinical Trials
15,177,490 Total Patients Enrolled
2 Trials studying Cystinuria
60 Patients Enrolled for Cystinuria
Marshall Stoller, MDPrincipal InvestigatorUniversity of California, San Francisco
1 Previous Clinical Trials
100 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a serious illness that is likely to cause death within the next 5 years.I am 18 years old or older.I am unable to understand and agree to the study's procedures and risks.I have been diagnosed with diabetes (type I or II).My primary language is not English.People who are in jail or prison.I have had cystine kidney stones in the past.I have had cystine kidney stones in the past.You have been diagnosed with cystinuria based on tests of your urine or kidney stones.
Research Study Groups:
This trial has the following groups:- Group 1: Study Drug
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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