An interventional study of No Intervention in Non-alcoholic Steatohepatitis (NASH), sponsored by Regeneron Pharmaceuticals. Terminated at 50 sites in 5 countries. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2023-03-17.
Sponsored by Regeneron Pharmaceuticals · Not applicable, Interventional, and Screening
Collection of clinical and genetic data to help identify individuals that carry genetic variants of known importance in Non-alcoholic Steatohepatitis (NASH)
1,451 studies on the registry are indexed under Fatty Liver; 292 are open to participants now.
This study's enrollment of 5,311 is above the median of 60 across 1,003 interventional studies indexed under Fatty Liver.
Browse Fatty Liver studies →Regeneron Pharmaceuticals is the lead sponsor of 400 studies on the registry; 91 are open to participants now.
Of its 120 completed or terminated interventional studies of FDA-regulated products, 77 (64%) have results posted.
Counted across the registry records on this site, refreshed daily.
Key Inclusion Criteria:
One or more of the following:
Evidence of NAFLD by imaging or liver histology as described in the protocol
A clinical suspicion of NASH based on presence of 2 or more elements of the metabolic syndrome defined by:
Key Exclusion Criteria:
Note: Other protocol-defined Inclusion/ Exclusion Criteria apply
Procedure: No Intervention
Single blood draw
Genotype frequencies of rs72613567 in Hydroxysteroid 17β dehydrogenase 13 (HSD17B13)
Time frame: Day 1
Genotype frequencies of rs738409 in patatin-like phospholipase domain containing 3 (PNPLA3)
Time frame: Day 1
Distribution of fibrosis-4 (FIB-4) scores across participants with different genotypes of rs72613567 in HSD17B13
Time frame: Day 1
Distribution of FIB-4 scores across participants with different genotypes of rs738409 in PNPLA3B13
Time frame: Day 1
This study is terminated, as verified in Mar 2023. You cannot join it, but the record below documents what was studied.
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Regeneron Pharmaceuticals