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Clinical Trials in Italy / NCT07211685
Active, not recruiting Phase 2

A Study to Learn About How Well BAY 3401016 Works in Adults With Alport Syndrome

NCT07211685 · tracked via the Priya Life Science Italy tracker
Sponsor
Phase
Phase 2
Started
2025-11-19
Last updated
2026-09-18

Condition(s) studied

Alport Syndrome

Investigational drug(s) / intervention(s)

BAY 3401016Placebo

BAY 3401016: BAY 3401016

Placebo: Placebo to BAY 3401016

Study summary

Alport syndrome (AS) is a rare genetic condition that causes kidney disease, hearing loss, and eye abnormalities that occur due to changes in specific genes (COL4A3, COL4A4, and COL4A5). These genes help in producing an important protein called collagen. People with AS have a high risk of developing chronic kidney disease (CKD), a condition in which there is progressive loss in kidney function over time. The kidneys soon lose their ability to remove waste products from the body properly, resulting in end-stage kidney disease. A common sign of decreasing kidney function is the presence of excess protein in the urine that is not usually found with healthy kidneys. This condition is known as proteinuria. The study drug, BAY 3401016 (a monoclonal antibody), is a type of medicine that blocks a protein called Semaphorin 3A (Sema3A), which is thought to be involved in causing kidney damage in AS. By blocking the action of the Sema3A protein, BAY 3401016 may prevent proteinuria and slow down the loss in kidney function due to AS.

The main purpose of this study is to learn more about how well BAY 3401016 works in slowing down the loss in kidney function in adults with a rapidly progressing AS.

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * Participants must be 18 to 45 years of age inclusive * Participants with AS, either XLAS (male) or ARAS (male or female) * eGFR ≥ 45 mL/min/1.73m2 * UACR ≥ 500mg/g Exclusion Criteria: * Chronic kidney disease is different from AS * Clinically significant illness that could have influence on the safety of the participant and/or interfere with the study objectives * History or current existence of malignancy * Participants with history of severe allergies, multiple drug allergies or non-allergic drug reactions including allergies affecting the lower respiratory tract - allergic asthma, allergies requiring therapy with corticosteroids or urticaria * Participants with active skin disorders (e.g. atopic dermatitis, severe acne) * Systolic blood pressure above 140 mmHg * Diastolic blood pressure above 90 mmHg

Primary outcome measure(s)

Trial sites (58)

FacilityCityRegionStatus
Nephrology Clinic at The Kirklin Clinic of UAB Hospital Birmingham Alabama
The Peggy and Harold Katz Family Drug Discovery Center - Nephrology Miami Florida
Center for Advanced Pediatrics - Nephrology Atlanta Georgia
Cardio Renal Institute Chubbuck Idaho
Tufts Medical Center | Nephrology Department Boston Massachusetts
Renal Disease Research Institute | Landry Dallas Texas
Clinica de Nefrologia, Urologia y Enfermedades Cardiovasculares S.A. Santa Fe Santa Fe Province
Hospital Británico Buenos Aires Argentina
Centro de Educacion Medica e Investigaciones Clinicas "Norberto Quirno" (CEMIC) Buenos Aires Argentina
Centro de Rehabilitacion Cardiovascular | San Luis, Argentina San Luis Argentina
St Joseph's Healthcare Hamilton | Cardiology Hamilton Ontario
University Hospital | Nephrology London Ontario
Lakeridge Health | Nephrology Whitby Ontario
Montreal General Hospital | Nephrology Montreal Quebec
Centre hospitalier universitaire de Québec (CHUQ) | Nephrology Québec Canada
Peking University First Hospital - Department of Pediatrics Beijing Beijing Municipality
Children's Hospital of Chongqing Medical University - Department of Nephrology Chongqing Chongqing Municipality
The First Affiliated Hospital, Sun Yat-sen University - Department of Pediatrics Guangzhou Guangdong
Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology - Pediatric Nephrology and Immunology Wuhan Hubei
Children's Hospital, Zhejiang University School of Medicine - Department of Nephrology Hangzhou Zhejiang
Fakultní nemocnice Hradec Kralové - Nefrologická klinika Hradec Králové Hradec Králové Region
Všeobecná fakultní nemocnice v Praze - Klinika nefrologie Prague Prague
CHU de Brest - Hopital La Cavale Blanche - Service de Nephorologie-Hémodialyse-Transplantation Brest Brittany Region
Centre Hospitalier Universitaire (CHU) de Toulouse - Hopital de Rangueil - Nephrologie et transplantation d'organes Toulouse Occitanie
Assistance Publique-Hopitaux de Paris (AP-HP) - Hopital Necker-Enfants Malades - Service d'Hopital De Jour Néphrologie adulte Paris Île-de-France Region
Universitaetsklinikum Erlangen - Medizinische Klinik 4, Nephrologie, Hypertensiologie Erlangen Bavaria
Universitaetsmedizin Goettingen (UMG) - Klinik fuer Nephrologie und Rheumatologie Göttingen Lower Saxony
Universitaetsklinikum Koeln - Klinik II fuer Innere Medizin - Nephrologie, Rheumatologie, Diabetologie, Innere Medizin Cologne North Rhine-Westphalia
Charité Mitte - Nephrologie und Internistische Intensivmedizin Berlin Germany
Mavani Research Center Ahmedabad Gujarat
All India Institute of Medical Sciences (AIIMS) - New Delhi New Delhi National Capital Territory of Delhi
K.G. Hospital Coimbatore Tamil Nadu
The Institute of Post Graduate Medical Education & Research (IPGMER) (SSKM Hospital) Kolkata West Bengal
Azienda Ospedaliero-Universitaria Di Bologna IRCCS_Policlinico Sant'Orsola - Nefrologia, Dialisi e Trapianto Bologna Italy
Azienda Socio Sanitaria Territoriale Degli Spedali Civili Di Brescia - Nefrologia Brescia Italy
IRCCS Istituto Giannina Gaslini - Nefrologia e Trapianto Rene Genova Italy
Ospedale Pediatrico Bambino Gesù - Nefrologia Roma Italy
Japanese RedCross Aichi Medical Center Nagoya Daini Hospital Nagoya Aichi-ken
Kobe University Hospital Kobe Hyōgo
Saitama Prefectural Children's Medical Center Chuo-Ku Tokyo

+ 18 more sites — see the full list on the official registry below.

More Bayer trials in Italy

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07211685 on ClinicalTrials.gov ↗ ← All trials in Italy