IgAN - IgA Nephropathy

3

Review clinical trials related to IgAN - IgA Nephropathy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Phase II Clinical Study on the Efficacy and Safety of QLS7305 in Patients With Kidney Disease (Part A)

QLS7305 injection is a chemically synthesized double-stranded small interfering RNA (siRNA) targeting complement C3, covalently linked to a ligand containing N-acetylgalactosamine (GalNAc) residues. After subcutaneous (SC) administration, it can inhibit C3 synthesis through the RNA interference (RNAi) mechanism, reduce circulating C3 protein levels, decrease the generation of complement-activated C5 convertase, and inhibit complement pathway activation. It is expected to become an effective treatment for complement-mediated kidney diseases and hematological disorders.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Qilu Pharmaceutical Co., Ltd.Updated: Jul 28, 2026Locations: 1
Eligibility criteria

Body weight ≥ 40 kg, Body Mass Index (BMI) < 32.5 kg/m² [+6]

Renal biopsy pathology indicates tubular atrophy or interstitial fibrosis exceed... [+21]

Status: Not yet recruiting

RD06-05 Universal CD19/BCMA CAR-T for Refractory Pediatric Autoimmune Diseases

This is a single-arm, open-label, phase I clinical study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of RD06-05, a universal CD19/BCMA dual-targeting chimeric antigen receptor T-cell (CAR-T), in pediatric and adolescent patients with refractory autoimmune diseases, including systemic lupus erythematosus/lupus nephritis (SLE/LN), systemic sclerosis (SSc), idiopathic inflammatory myopathy (IIM), multidrug-resistant nephrotic syndrome (MDR-NS), and refractory IgA nephropathy (IgAN). Approximately 30 eligible patients will be enrolled and receive a single intravenous infusion of RD06-05 at an initial dose of 6×10⁶ CAR+ T cells/kg, with a potential dose escalation to 10×10⁶ CAR+ T cells/kg following review by a Safety Review Committee (SRC).

Participants needed: 30
Trial details
Phase: Early Phase 1Age: 5-20Biological sex: AllType: InterventionalSponsor: The Children's Hospital of Zhejiang University School of MedicineUpdated: Jun 29, 2026Locations: 2
Eligibility criteria

Voluntary participation with signed informed consent from patient or legal guard... [+20]

Co-existing autoimmune disease that may interfere with disease activity attribut... [+38]

Status: Recruiting

Anti-CD19/BCMA CAR-NK Cells in Patients With B Cell Mediated Autoimmune Disease

this is an investigator-initiated trial aimed at evaluating the efficacy and safety of anti-CD19/BCMA CAR-NK Cells in Patients With B cell mediated autoimmune disease.

Participants needed: 36
Trial details
Phase: Early Phase 1Age: 3+Biological sex: AllType: InterventionalSponsor: The Children's Hospital of Zhejiang University School of MedicineUpdated: Dec 1, 2025Locations: 1
Eligibility criteria

Patients or their legal guardians must acknowledge the risks and procedures invo... [+22]

Subjects with known severe allergic reactions, hypersensitivity, contraindicatio... [+17]