Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06854640
PHASE1

A Study to Learn About How Safe BAY 3389934 is, Its Suitable Dose, and How it Affects the Participants With Sepsis Induced Coagulopathy

Sponsor: Bayer

View on ClinicalTrials.gov

Summary

Researchers are looking for a better way to treat people who have sepsis induced coagulopathy. Sepsis happens when bacteria and their toxins spread in the blood, causing an infection. To overcome the infection the body responds activating the immune system, sometimes this immune response is too active and causes uncontrolled blood clot formation, also called sepsis-induced coagulopathy. Sepsis coagulopathy damages blood vessels and organs and leads to low platelet levels in the body. In severe cases, it can even lead to death. The main purpose of this first in patient study is to learn about how safe BAY 3389934 is, its suitable dose, and how it affects the participants with sepsis induced coagulopathy. For this study, researchers will enroll people receiving treatment for sepsis induced coagulopathy in a hospital intensive care unit (ICU). For this, the researchers will collect the number of participants with medical problems during and after receiving BAY 3389934. These medical problems are also known as "adverse events". Doctors keep track of all medical problems that happen in studies, even if they do not think they might be related to the study treatments. Participants will be divided into 2 groups. The first group will receive the lowest starting dose of BAY3389934. The researcher will carefully monitor how the participant responds to the medication and may adjust the dose, either increasing or decreasing it based on the safety and the tolerability of the drug. If no serious side effects are reported from the first group, the second group will receive higher dose of BAY3389934. Each participant will be in the study for around 28 days. During the study, the doctors and their study team will: * Take blood and urine samples, * Do physical examinations, * Check vital signs such as body temperature, blood pressure and heart rate, * Examine heart health using electrocardiogram (ECG)

Official title: First in Patient, Dose Escalation, Open Label Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous Infusion of BAY 3389934 to Patients With Sepsis Induced Coagulopathy

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

36

Start Date

2025-03-12

Completion Date

2027-02-28

Last Updated

2026-03-27

Healthy Volunteers

No

Interventions

DRUG

BAY3389934

Solution for IV infusion

Locations (20)

UZ Antwerpen - Intensive Care

Edegem, Belgium

Centre Hospitalier Universitaire (CHU) de Liege - Domaine Universitaire du Sart Tilman - Intensive Care

Liège, Belgium

Clinique Saint-Pierre d'Ottignies - Intensive Care

Ottignies-Louvain-la-Neuve, Belgium

Universite Catholique de Louvain (UCL) - Cliniques Universitaires Saint-Luc - Intensive Care

Woluwe-Saint-Lambert, Belgium

CHRU de Tours - Hôpital Bretonneau - Médecine Intensive Réanimation

Tours, Centre-Val de Loire, France

Hopitaux Universitaires de Strasbourg Nouvel Hopital Civil - Service de Médecine Intensive Réanimation

Strasbourg, Grand Est, France

Centre Hospitalier Universitaire de Limoges Dupuytren 1 - Service de réanimation polyvalente

Limoges, Nouvelle-Aquitaine, France

Centre Hospitalier Universitaire d'Angers - Médecine Intensive Réanimation et Médecine Hyperbare

Angers, Pays de la Loire Region, France

Centre Hospitalier Départemental Vendée - Service de réanimation polyvalente

La Roche-sur-Yon, Pays de la Loire Region, France

Hopital Hotel Dieu Nantes - Service de Médecine Intensive Réanimation

Nantes, Pays de la Loire Region, France

Hôpital Raymond-Poincaré - Service de Médecine Intensive - Réanimation, Médecine Hyperbare

Garches, Île-de-France Region, France

Kliniken der Stadt Köln gGmbH - Krankenhaus Merheim - Lungenklinik

Cologne, North Rhine-Westphalia, Germany

Universitaetsklinikum Carl Gustav Carus an der Technischen Universitaet Dresden | Medizinische Klinik I - FB Haemostaseologie

Dresden, Germany

Universitätsklinikum Leipzig AöR | Interdisziplinare Internistische Intensivmedizin

Leipzig, Germany

Klinikum der Universität München AöR - Klinik für Anaesthesiologie (Campus Großhadern)

München, Germany

Jeroen Bosch Ziekenhuis - Intensive Care

's-Hertogenbosch, Netherlands

Medisch Spectrum Twente - Intensive Care

Enschede, Netherlands

Universitair Medisch Centrum St. Radboud - Intensive Care

Nijmegen, Netherlands

Canisius WIlhelmina Ziekenhuis - Intensive Care

Nijmegen, Netherlands

Erasmus Medisch Centrum - Intensive Care

Rotterdam, Netherlands