New drug aims to protect kidneys in rare genetic disease
NCT ID NCT06274489
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new drug, setanaxib, in 20 people with Alport syndrome, a genetic condition that damages kidneys. The goal was to see if the drug is safe and can help preserve kidney function when added to standard care. Participants took either setanaxib or a placebo for 24 weeks, and researchers monitored side effects and kidney health through blood and urine tests.
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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
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Locations
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AP-HP Hopital Necker-Enfants Malades
Paris, 75015, France
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Fakultni Nemocnice Hradec Kralove
Hradec Králové, Czechia
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Fakultni Nemocnice Olomouc
Olomouc, Czechia
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Fundacio Puigvert
Barcelona, 08025, Spain
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Great Ormond Street Hospital for Children
London, WC1N 3JH, United Kingdom
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Hospital Clinic Barcelona
Barcelona, 08036, Spain
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Hospital Fundacion Jimenez Diaz
Madrid, 28040, Spain
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Hospital Universitario 12 de Octubre
Madrid, Usera, 28041, Spain
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Hospital Universitario Reina Sofia
Córdoba, 14004, Spain
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Hospital Universitario Vall d'Hebron
Barcelona, Spain
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Hospital Universitario Virgen de las Nieves
Granada, 18014, Spain
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Institut Klinicke a Experimentalni Mediciny
Prague, Czechia
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Medizinische Universitaet Wien
Vienna, State of Vienna, 1090, Austria
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Nottingham City Hospital
Nottingham, United Kingdom
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Royal Free London NHS Foundation Trust
London, NW3 2QG, United Kingdom
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Royal Manchester Children's Hospital
Manchester, M13 9WL, United Kingdom
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Vseobecna Fakultni Nemocnice v Praze
Prague, Czechia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Study links gum health to rare kidney diseases
- Alport patients needed: join a registry to speed up research
- Kidney hope: drug combo may slow alport disease
- New drug aims to slow kidney damage in rare alport syndrome
- Experimental drug targets genetic cause of alport syndrome in tiny pilot