drugset / Trial / NCT07619131

A Phase III Study to Assess the Effect of FDC Laroprovstat/Rosuvastatin Compared With Laroprovstat, Rosuvastatin and Placebo on LDL-C in LLT-naïve Patients.

NCT07619131

Phase 3 Not yet recruiting 600 enrolled AstraZeneca
RandomizedFactorialQuadruple-blindTreatment

Summary

This is a study to evaluate the effect on LDL-C and the safety and tolerability of FDC laroprovstat/rosuvastatin in LLT-naïve patients. Laroprovstat is a small molecule that reduces the amount of LDL-C in the blood. Laroprovstat and FDC laroprovstat/rosuvastatin are being developed for the treatment of hypercholesterolaemia.

Timeline

Start
2026-08-17
Primary completion
2027-07-30
Completion
2027-07-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Laroprovstat Small molecule Oral
Comparator Rosuvastatin Small molecule Oral

Indications