Source-defined biomarker
HepQuant DSI as a Reasonably Likely Surrogate Endpoint (RLSE) for Clinical Outcome in Compensated Cirrhosis due to Metabolic Dysfunction-Associated Steatohepatitis (MASH)
This exact source name has not been reconciled to a broader biomarker identity.
HepQuant DSI as a Reasonably Likely Surrogate Endpoint (RLSE) for Clinical Outcome in Compensated Cirrhosis due to Metabolic Dysfunction-Associated Steatohepatitis (MASH) is a source-defined biomarker in the evidence tier "FDA qualification project". This page lists evidence by type: FDA biomarker qualification projects (1), each linked to its source.
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FDA qualification project
Source-level evidence only
FDA biomarker qualification projects (1)
Shown in this order: most recent snapshot first.
| Project | DDT number | Source status | Submitter | Biomarker role |
|---|---|---|---|---|
| HepQuant DSI as a Reasonably Likely Surrogate Endpoint (RLSE) for Clinical Outcome in Compensated Cirrhosis due to Metabolic Dysfunction-Associated Steatohepatitis (MASH) | DDT-BMQ-000175 | Project status: Not accepted | HepQuant LLC | Not assigned |
Not on this page
Checked, with nothing recorded for this biomarker: fda companion diagnostic assertions and assay-provider ledger.