Could a common drug shield kidneys from protein damage?
NCT ID NCT02343094
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether sodium phenylbutyrate, a drug already used for other conditions, can reduce a marker of kidney injury in people with proteinuric kidney disease. 26 participants took the drug for 14 days. The goal was to see a 50% drop in a urine marker called Lcn2, which signals kidney stress.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sodium phenylbutyrate
- What this could lead to
- If it works, this could point toward a new treatment to protect kidneys in people with proteinuric kidney disease.
- What could go wrong
- This is a small, early-phase trial with only 26 participants. It measures a lab marker, not long-term kidney health, so success is uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
26 people
The number who actually took part.
- Start date
-
Feb 2015
- Finished
-
Jul 2016
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Chronic Kidney disease for ore than 3 months * Proteinuria \> 1g/d or 0,1g/mmmol creatinine * eGFR \>30ml/mn/1,73m2 * written informed consent * affiliated with social security health insurance Exclusion Criteria: * Women with childbearing potential * Recent (\<3 months) modification of ACE inhibitors or ARB * Acute renal failure * eGFR \<30ml/mn/1,73m2 * Nephrotic syndrome (albuminélia \<30g/l) * Infection with HIV, HCV, HBV * Liver insufficiency * No affiliated with social security health insurance * inclusion in another protocol of biomedical research * risk of non-adherence to protocol and visits * patients having a cardiac insufficiency of grade 3 or 4 * patient requiring of a strict salt-free diet * patients under corticoids or immunosuppresseurs * clinical intolerance in the treatment * intolerance in the fructose, the syndrome of malabsorption glucose and galactose or a deficit in sucrase / isomaltase * patients treated by Probenecide
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Hôpital Necker Enfants Malades
Paris, 75015, France
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