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

Generation of Skin Fibroblast Banks, Urine-derived Cells and Biomarker Isolation From Patients With Amyotrophic Lateral Sclerosis (Als)

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07099066
Acronym
HCD-SLA
Enrollment
50
Registered
2025-08-01
Start date
2025-09-01
Completion date
2026-06-30
Last updated
2025-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amyotrophic Lateral Sclerosis (ALS)

Keywords

Amyotrophic Lateral Sclerosis (ALS)

Brief summary

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

Detailed description

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.

Interventions

3 types of sampling : urine, skin and blood.

Sponsors

Human Cell Design
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Cell banking8 monthsNumber of cell batches cryopreserved that meet predefined quality criteria (cell viability ≥ 80%, absence of mycoplasma). Data will be summarized as percentage of compliant batches over total batches produced.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026