C3 Glomerulopathy (C3G)

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Review clinical trials related to C3 Glomerulopathy (C3G). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Real-World Effectiveness and Safety of Pegcetacoplan in Patients With C3G or IC-MPG: A Multi-Country Study

The purpose of this study is to evaluate the effectiveness and safety of Pegcetacoplan in patients with C3G and primary IC-MPGN in the real-world setting. This study will also assess biomarkers not routinely measured in clinical practice. Results will support the long-term evaluation of the benefit-risk profile of pegcetacoplan in a broad patient population, informing clinical decision-making.

Participants needed: 150
Trial details
Phase: Phase 4Biological sex: AllType: InterventionalSponsor: Swedish Orphan BiovitrumUpdated: Aug 5, 2026Locations: 101
Eligibility criteria

Have received or plan to receive pegcetacoplan for the treatment of C3G or prima... [+1]

Receiving an investigational treatment for C3G or primary IC-MPGN at the time of... [+1]

Status: Recruiting

A Clinical Trial to Test the Safety, Tolerability, and How the Body Processes CPV-104 in Healthy People and Patients With C3-Glomerulopathy

This study is the first time the new medicine CPV-104 is being tested in people. CPV-104 is designed to regulate the complement system, which can be overactive in diseases such as C3 glomerulopathy (C3G), an ultra-rare kidney disorder. The study includes healthy adults and adult patients with C3G to assess safety, tolerability, how the body processes the medicine, and whether the immune system reacts to it. The study is divided in two part; in Part 1 (SAD), healthy volunteers receive one IV dose of CPV-104 or a placebo while in Part 2 (MAD) patients with C3G receive four weekly IV doses of CPV-104 (no placebo). Participants will have close monitoring, including side-effect checks, blood and urine tests, ECGs, vital signs, and blood samples to measure drug levels and antibodies. For those with C3G, researchers will also observe kidney function, although the main goal is safety, not testing effectiveness. A Safety Review Committee will regularly review results to ensure it is safe to continue to the next dose or study group.

Participants needed: 39
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: eleva GmbHUpdated: Jul 31, 2026Locations: 17
Eligibility criteria

Participants must be at least 18 years old and no more than 50 years old, at the... [+1]

Body weight within 50 kg for male/ 45 kg for female to 110 kg and BMI within the... [+52]

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: Available

Managed Access Programs for LNP023, Iptacopan

The purpose of this registration form is to list all Managed Access Programs (MAPs) related to LNP023, Iptacopan

Trial details
Age: 18+Biological sex: AllType: Expanded AccessSponsor: Novartis PharmaceuticalsUpdated: Dec 5, 2025
Eligibility criteria

An independent request should be received from a licensed physician (in some ins... [+6]