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PhenotYpe Research for ALS ModIfyer Discovery.

PhenotYpe Research for ALS ModIfyer Discovery.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON26294
Enrollment
600
Registered
2013-03-13
Start date
2013-06-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

ALS, MND, amyotrophic lateral sclerosis

Interventions

None listed

Sponsors

University Medical Center Utrecht, the Netherlands Vesalius Research Center, VIB, Leuven, Belgium University Hospital Jena, Germany
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients with ALS.

Exclusion criteria

Exclusion criteria: N/A

Design outcomes

Primary

MeasureTime frame
1. Report on key molecular drivers in transcriptomic data related to disease progression (month 35); 2. Report on key molecular drivers in methylation data related to disease progression (month 35); 3. Report on key molecular drivers in proteomic data related to disease progression (month 35); 4. Report on longitudinal MRI and MUNIX changes related to disease progression (month 35).

Secondary

MeasureTime frame
1. Tender document for appropriate SMEs that describes most promising therapeutic targets, based on differential co-expression, co-methylation and co-translation reports; 2. Tender document for appropriate SMEs that describes most promising molecular disease progression markers based on those markers that best discriminate between fast and slow progressors.

Contacts

Public ContactPetra Berk

UMC Utrecht Dept Neurology, G03.232 Heidelberglaan 100

P.A.Berk@umcutrecht.nl+31 (0)88 7551221

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)