drugset / Trial / NCT04652349

Efficacy and Safety of HGP1910 and HCP1903 in Patients With Primary Hypercholesterolemia

NCT04652349 ↗

Phase 3 Completed 279 enrolled Hanmi Pharmaceutical Company Limited
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to investigate the safety and clinical efficacy of HGP1910 and HCP1903 in patients with primary hypercholesterolemia

Timeline

Start
2020-07-06
Primary completion
2020-12-17
Completion
2021-01-14

Outcome

Met primary endpoint

paper A greater decrease in the LDL cholesterol levels (primary endpoint) were found in the R2.5+E10 group (-45.7±18.6%) than in the E10 group (-16.7±14.7%, p<0.0001) PMID 34429197 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject HCP1903 Unknown — Oral
Comparator HGP1909 Unknown — Oral
Subject HGP1910 Unknown — Oral
Comparator HGP1911 Unknown — Oral

Indications