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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
An Open-Label Phase 2 Study of N-Acetyl-D-Mannosamine (ManNAc) in Subjects With Podocyte DiseasesFemale Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Urination Disorders, Urogenital Diseases, Urological Manifestations, autoimmune disease, focal segmental glomerulosclerosis, glomerulonephritis, immune system disorder, kidney disorder, macular corneal dystrophy, membranous glomerulonephritis, minimal change disease, nephritis, nephrosis, proteinuria, urinary system disorderRecruitingPhase 22026-10-09NCT06664814
Virotherapy and Natural History Study of KHSV-Associated Multricentric Castleman s Disease With Correlates of Disease ActivityBlood-Borne Infections, Genital Diseases, HIV infectious disease, Hemic and Lymphatic Diseases, Infections, Lymphadenopathy, Multi-centric Castleman's Disease, RNA Virus Infections, Urogenital Diseases, cancer, immune system disorder, immunoproliferative disorder, inborn error of immunity, infectious disease, lentivirus infection, lymphatic system disorder, lymphoproliferative syndrome, macular corneal dystrophy, neoplasm, sexually transmitted disease, uterine carcinosarcoma, viral infectious disease, viral sexually transmitted diseaseActive, not recruitingPhase 22026-10-08NCT00092222
A Study to Evaluate the Safety, Tolerability and PK of SK-09focal segmental glomerulosclerosis, macular corneal dystrophyRecruitingPhase 12026-09-03NCT07267026
Sirolimus in Previously Treated Idiopathic Multicentric Castleman DiseaseCastleman disease, Hemic and Lymphatic Diseases, Multi-centric Castleman's Disease, immune system disorder, immunoproliferative disorder, lymphatic system disorder, lymphoproliferative syndrome, macular corneal dystrophyActive, not recruitingPhase 22026-08-20NCT03933904
Fresh Corneal Lenticule Implantation in Macular Corneal Distrophy With Relex Smile SurgeryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, corneal disorder, corneal dystrophy, eye disorder, hereditary disease, macular corneal dystrophyEnrolling by invitationNot applicable2026-07-29NCT04642729
Atacicept in Multiple Glomerular DiseasesFemale Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, IgA glomerulonephritis, Male Urogenital Diseases, Urogenital Diseases, autoimmune disease, focal segmental glomerulosclerosis, glomerulonephritis, immune system disorder, kidney disorder, macular corneal dystrophy, nephritis, nephrosis, nephrotic syndrome, urinary system disorderRecruitingPhase 22026-06-26NCT06983028
NEPTUNE Match StudyAlport syndrome, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Nephrotic Syndrome, Minimal Change, Skin and Connective Tissue Diseases, Urogenital Abnormalities, Urogenital Diseases, autoimmune disease, connective tissue disorder, focal segmental glomerulosclerosis, glomerulonephritis, hereditary nephritis, immune system disorder, kidney disorder, macular corneal dystrophy, membranous glomerulonephritis, minimal change disease, nephritis, nephrosis, nephrotic syndrome, urinary system disorderRecruitingNot applicable2026-06-10NCT04571658
Nephrotic Syndrome Study NetworkFemale Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Urogenital Diseases, autoimmune disease, focal segmental glomerulosclerosis, glomerulonephritis, immune system disorder, kidney disorder, macular corneal dystrophy, membranous glomerulonephritis, minimal change disease, nephritis, nephrosis, nephrotic syndrome, urinary system disorderRecruitingNot stated2026-06-10NCT01209000
Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular DiseasesAlport syndrome, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Hemorrhage, IgA glomerulonephritis, Male Urogenital Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Skin Manifestations, Skin and Connective Tissue Diseases, Urogenital Abnormalities, Urogenital Diseases, autoimmune disease, blood coagulation disease, cardiovascular disorder, connective tissue disorder, focal segmental glomerulosclerosis, glomerulonephritis, hematologic disorder, hemorrhagic disease, hereditary nephritis, immune system disorder, immunoglobulin A vasculitis, kidney disorder, macular corneal dystrophy, minimal change disease, nephritis, nephrosis, purpura, skin disorder, skin vascular disease, type III hypersensitivity disease, urinary system disorder, vascular disorder, vascular hemostatic disease, vasculitisRecruitingPhase 22026-05-12NCT05003986
Recurrence Post-transplant Observational Study in Focal Segmental Glomerulosclerosis and Minimal Change DiseaseDisease Attributes, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Recurrence, Urogenital Diseases, focal segmental glomerulosclerosis, glomerulonephritis, kidney disorder, macular corneal dystrophy, minimal change disease, nephritis, nephrosis, urinary system disorderRecruitingNot stated2026-04-29NCT05650619
International Registry for Patients With Castleman DiseaseCastleman disease, Hemic and Lymphatic Diseases, Multi-centric Castleman's Disease, immune system disorder, immunoproliferative disorder, lymphatic system disorder, lymphoproliferative syndrome, macular corneal dystrophyRecruitingNot stated2026-03-03NCT02817997
The FOrMe Registry (The German Focal Segmental Glomerulosclerosis and Minimal Change Disease Registry)Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Urogenital Diseases, focal segmental glomerulosclerosis, glomerulonephritis, idiopathic nephrotic syndrome, kidney disorder, macular corneal dystrophy, minimal change disease, nephritis, nephrosis, nephrotic syndrome, urinary system disorderRecruitingNot stated2025-09-17NCT03949972