Generation of Cell Banks and Biomarker Isolation From Patients With Amyotrophic Lateral Sclerosis (ALS) (HCD-SLA)

NCT ID: NCT07099066

Last Updated: 2025-08-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-01

Study Completion Date

2026-06-30

Brief Summary

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The aim of this research is to establish different cell banks from patients with amyotrophic lateral sclerosis (ALS).

Detailed Description

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The objective of this research is to:

* Create banks of skin fibroblasts from skin biopsy samples
* Create banks of urine-derived cells (UDCs) from urine samples
* Build a collection of blood samples to enable isolation of biomarkers.

Conditions

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Amyotrophic Lateral Sclerosis (ALS)

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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ALS patients

sampling blood

Intervention Type OTHER

3 types of sampling : urine, skin and blood.

Interventions

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sampling blood

3 types of sampling : urine, skin and blood.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Subjects over 18 years old;
* Subjects who have given their consent and signed an informed, free and express consent form;
* Subjects with diagnosed ALS;
* Subjects affiliated to or benefiting from a social security scheme.

Exclusion Criteria

* Subjects with contraindications to the collection of biological samples (blood, skin, urine).
* Subjects undergoing treatment likely to affect hemostasis (anticoagulants, platelet anti-aggregants, etc.) in the month prior to inclusion and during the study;
* Subjects with hereditary or acquired haemostasis disorders;
* Subjects who have undergone physical treatment (radiotherapy, etc.) on the area to be biopsied in the last 6 months;
* Lidocaine-intolerant subjects;
* Subjects who have reached the age of majority and are subject to a protective measure or are unable to express their consent.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Human Cell Design

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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2025-A00776-43

Identifier Type: -

Identifier Source: org_study_id

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