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NCT04943978

Prospective Studies on Immunopathogenesis of Liver Fibrosis

Status unknown Last updated 29 June 2021
What this trial tests

trial in Chronic Liver Disease in 1,000 participants. Status unknown.

Timeline
1 February 2014
Primary endpoint
31 January 2023
31 January 2026

Quick facts

Lead sponsorUniversity of Regensburg
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment1,000
Start date1 February 2014
Primary completion31 January 2023
Estimated completion31 January 2026
Sites1 location across Germany

Conditions studied

Sponsor

University of Regensburg

Who can join

18 and older, any sex, with Chronic Liver Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The immune system is thought to play a key role in the development of liver inflammation and subsequent liver fibrosis or cirrhosis. In the case of viral hepatitis and autoimmune hepatitis, for example, numerous studies have focused on the acquired antigen-specific immunity. However, the liver is the site of increased occurrence of the components of the innate immune response (NK and NKT cells) and, in contrast to T cells, these T cells, these do not require antigen presentation. Therefore, the present study was designed to determine which cellular components of the (NK, NKT, dendritic cells, macrophages) or the acquired immune response (CD4, CD8) or which network of immune cells is involved in the immunopathogenesis of progressive liver inflammation or the development of liver fibrosis. The aim is to identify lymphocyte populations that exhibit either prognostically favorable or unfavorable characteristics. This should allow conclusions to be drawn for a more targeted and individualized therapy of the respective chronic liver diseases.

Publications & conference data

3 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Soluble CD46 as a diagnostic marker of hepatic steatosis.
    Bitterer F, Kupke P, Adenugba A, Evert K, et al · · 2024 · cited 5× · PMID 38838471 · DOI 10.1016/j.ebiom.2024.105184
  2. Proteolytic shedding of CD46 from human hepatocytes indicates liver stress.
    Kupke P, Yang Zhou J, Glehr G, Riquelme P, et al · · 2024 · cited 1× · PMID 39698100 · DOI 10.1016/j.heliyon.2024.e40841
  3. Soluble CD46 improves detection of hepatic steatosis by contrast-enhanced computed tomography before liver surgery.
    Kupke P, Kupke LS, Glehr G, Evert K, et al · · 2025 · PMID 40277388 · DOI 10.1097/js9.0000000000002422

Verify or expand the search:

Other recruiting trials for Chronic Liver Disease

Currently open trials in the same condition.

Other University of Regensburg trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04943978.

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