Development programme
ESSENCE — semaglutide in steatohepatitis
A two-part trial in metabolic dysfunction-associated steatohepatitis. Part 1 reported histological endpoints; the clinical-outcome part had not reported at the assessment date.
A two-part trial in metabolic dysfunction-associated steatohepatitis. Part 1 reported histological endpoints; the clinical-outcome part had not reported at the assessment date.
Sponsor class: Manufacturer-sponsored. First record: 2021.
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Records in this programme
4 documents
Table 1. Trial records on this page. The table sorts on any column and filters on the controls above; both operate on the records shown on this page only.
| Record | Compound | Phase | Status | Design | Randomised | Year | Certainty |
|---|---|---|---|---|---|---|---|
| ESSENCE | Semaglutide | Phase 3 | Reported | Randomised, double-blind, placebo-controlled | 1,197 | 2025 | Moderate |
| ESSENCE-DDIprogramme record | Semaglutide | Phase 1 | Reported | Randomised crossover | — | 2025 | Very low |
| ESSENCE-PKprogramme record | Semaglutide | Phase 1 | Reported | Phase 1 ascending dose | — | 2025 | Very low |
| ESSENCE-RENAL-IMPprogramme record | Semaglutide | Phase 1 | Reported | Phase 1 ascending dose | — | 2025 | Very low |