Study Evaluating Patients With Cystinuria

PHASE2/PHASE3WithdrawnINTERVENTIONAL
0
Timeline

Start Date

May 1, 2024

Primary Completion Date

June 30, 2025

Study Completion Date

August 31, 2025

Conditions
Cystinuria
Interventions
DRUG

ADV7103

Patients receive ADV7103 twice a day at optimal dose.

DRUG

Standard of Care

Cohort of patients with cystinuria, matching-pair for age category to the patients of ADV7103 Cohort, will receive their own alkalinising treatment (SoC) taken at the usual dose and frequency and will follow their usual first intention treatment (hydration and diet) for a 2-year-period.

Trial Locations (13)

15013

CHU Pitié-Salpétrière, Paris

31059

CHU Purpan, Toulouse

33076

CHU de Bordeaux - Hôpital Pellegrin, Bordeaux

38043

CHU Grenoble, Grenoble

51092

Hôpital Américain CHU de Reims, Reims

51100

CHU Reims, Reims

59000

CHRU Lille, Lille

69500

Centre Hospitalier Universitaire de Lyon, Bron

75015

Hôpital Necker AP-HP, Paris

Hôpital Necker Enfants Malades, Paris

75020

Hôpital Ténon - Explorations fonctionnelles Mutlidisciplinaires et INSERM UMR S 1155, Paris

Unknown

Cliniques Universitaires Saint-Luc, Brussels

UZ Leuven, Gasthuisberg Hospital, Leuven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Advicenne Pharma

INDUSTRY

NCT04137978 - Study Evaluating Patients With Cystinuria | Biotech Hunter | Biotech Hunter