3 recruiting, 2 completed, 1 not yet recruiting. 1 Not applicable, 1 Phase 2.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 1 | Completed 1 |
| Phase 2 | 1 | Not yet recruiting 1 |
Follow Oculocerebrorenal Syndrome: new trials by email Literature Review of Oculocerebrorenal Syndrome trials Research Report on Oculocerebrorenal Syndrome
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| An Open-label, Phase 2 Pilot Study on the Efficacy and Safety of Piclidenoson in Patients With Lowe Syndrome Piclidenoson - Lowe Syndrome | Phase 2 | Not yet recruiting | Can-Fite BioPharma | 5 | 2026-06-01 | 2026-02-18 |
| Prospective Research Rare Kidney Stones (ProRKS) Hyperoxaluria, Cystinuria | Recruiting | Mayo Clinic | 220 | 2016-05-01 | 2026-08-07 | |
| Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford Rare Disorders, Undiagnosed Disorders | Recruiting | Sanford Health | 20000 | 2010-07-01 | 2025-05-29 | |
| National Registry of Rare Kidney Diseases Adenine Phosphoribosyltransferase Deficiency, AH Amyloidosis | Recruiting | UK Kidney Association | 35000 | 2009-11-06 | 2023-10-04 | |
| Study of the Pathophysiological Mechanisms Involved in Bleeding Events Blood sample - Oculocerebrorenal Syndrome | Not applicable | Completed | Assistance Publique - Hôpitaux de Paris | 30 | 2009-02-01 | 2025-11-20 |
| Genetic Analysis of Oculocerebrorenal Syndrome of Lowe Lowe Syndrome | Completed | National Human Genome Research Institute (NHGRI) | 120 | 2001-02-17 | 2017-07-02 |
Adenine phosphoribosyltransferase deficiency (2) · Atypical Hemolytic Uremic Syndrome (2) · Cystinosis (2) · Cystinuria (2) · Dent Disease (2) · Denys-Drash Syndrome (2) · Hyperoxaluria, Primary (2) · 3-Methylglutaconic Aciduria, Type V (1) · Achalasia Addisonianism Alacrimia syndrome (1) · Acrodysostosis (1) · Addison Disease (1) · Alagille Syndrome (1) · Alstrom Syndrome (1) · Amnesia, Transient Global (1)
Abnormalities, Multiple (6) · Amino Acid Transport Disorders, Inborn (6) · Brain Diseases (6) · Brain Diseases, Metabolic (6) · Brain Diseases, Metabolic, Inborn (6) · Central Nervous System Diseases (6) · Congenital Abnormalities (6) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (6) · Female Urogenital Diseases (6) · Female Urogenital Diseases and Pregnancy Complications (6) · Genetic Diseases, Inborn (6) · Genetic Diseases, X-Linked (6) · Kidney Diseases (6) · Male Urogenital Diseases (6) · Metabolic Diseases (6)
Assistance Publique - Hôpitaux de Paris (1) · Can-Fite BioPharma (1) · Mayo Clinic (1) · National Human Genome Research Institute (NHGRI) (1) · Sanford Health (1) · UK Kidney Association (1)
United States (3) · Australia (1) · Canada (1) · France (1) · Iceland (1) · Israel (1) · Italy (1) · United Kingdom (1)
John Lieske, MD (1)