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Validation of Ella Platform for Serum Nfl And GFAP Measures In Multiple Sclerosis Patients

Multi-Site Validation of Ella Platform for Serum Nfl And GFAP Measures In Multiple Sclerosis Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05352971
Acronym
Nf-Ella Loca
Enrollment
664
Registered
2022-04-29
Start date
2022-09-15
Completion date
2023-09-30
Last updated
2023-10-10

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

Conditions

Multiple Sclerosis

Brief summary

Serum neurofilament-light chain (NfL) and glial fibrillary acidic protein (GFAP) measured by single molecule array (SIMOA) are novel biomarkers of multiple sclerosis patients (MS) activity and progression. Its use is limited due to low availability and high costs. ELLA is a cheaper platform with increasing availability. Recently, we compared SIMOA and ELLA platforms to assess serum NfL levels in 203 MS patients from the OFSEP-HD study. There was a strong correlation (Spearman r = 0.86, p \< 0.0001) between both platforms. As for SIMOA, serum NfL levels measured by ELLA were correlated with age and EDSS and were significantly higher in active MS, suggesting that these assays are equivalent and can be used in any center for routine care. However, the accuracy of local measures acquired with ELLA has not been determined. The aim os this study is to assess the concordance of multi-site ELLA instruments, accuracy of GFAP measures as compared to SIMOA, and the predictive value of NfL and GFAP measured by ELLA in MS.

Interventions

OTHERBiomarker quantification

Patient blood samples will be tested on 2 different platforms

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients from the OFSEP HD cohort. * At least one native (no thaw-freeze cycle) serum sample in local or in centralized Biological Resource Center

Exclusion criteria

* No bio-collection or insufficient sample volume * No OFSEP minimal sheet at baseline

Design outcomes

Primary

MeasureTime frameDescription
Inter-laboratory reproducibility of neurofilament-light chain level measurementsDay 0Coefficients of variation will be calculated in 30 patients
Inter-laboratory repeatability of neurofilament-light chain level measurementsDay 0Serum from 3 patients with low, medium or high levels of NfL will be tested 10 times
Inter-laboratory reproducibility and repeatability of glial fibrillary acidic protein level measurementsDay 0Coefficients of variation will be calculated in 30 patients
Inter-laboratory repeatability of glial fibrillary acidic protein level measurementsDay 0Serum from 3 patients with low, medium or high levels of GFAP will be tested 10 times

Secondary

MeasureTime frameDescription
to build a global disease activity scoreDay 0Logistic regression to predict active multiple sclerosis
to build a global disability scoreDay 0Logistic regression to predict Expanded Disability Status Scale score
compare the GFAP values obtained using the ELLA and SIMOA platforms in MS patientsDay 0Intraclass concordance correlation coefficient and Passing-Bablock analysis calculated in 210 patients

Countries

France

Outcome results

None listed

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