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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04766736
Other study ID # 69HCL19_0258
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2019
Est. completion date December 31, 2022

Study information

Verified date February 2021
Source Hospices Civils de Lyon
Contact Fabien ZOULIM, Pr
Phone 4 26 10 93 55
Email fabien.zoulim@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Netrin-1 is a dependence receptor ligand participating in the pathology of several cancer types. It is up-regulated in chronic liver diseases, cirrhosis and HCC. We hypothesize that netrin-1 may play a detrimental role in HCC. The goal of this project is to characterize netrin-1 signals in HCC samples with ad hoc controls, to investigate the benefit of capturing netrin-1 in preclinical models of HCC and to try to define patients groups the most likely to benefit from this targeting approach in the clinic.


Recruitment information / eligibility

Status Recruiting
Enrollment 320
Est. completion date December 31, 2022
Est. primary completion date June 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - any patient suffering from HCC - age >18 - informed consent provided Exclusion Criteria: - absence of informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Quantification of netrin-1 signals by antibody-based approaches
Samples have been obtained upon curative surgery without any other therapy administered and subsequently characterized by pathologists after FFPE inclusion.

Locations

Country Name City State
France Hepatogastroenterology service of the Croix-Rousse Hospital Lyon

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Netrin-1 expression patterns in HCC samples Netrin-1 expression levels will be quantified by immunoblotting with ad hoc internal standards. Positivity threshold by IHC will be evaluated using ad hoc positive and negative control tissues. The densitometry approach will be used. Outcome measure is to be performed after surgery of the tumors (at least 1 year later). It has no impact on the patient's care.
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