A PHASE III RANDOMISED, DOUBLE-BLIND, PARALLEL-GROUP STUDY TO ASSESS THE EFFECT OF FIXED DOSE COMBINATION LAROPROVSTAT/ROSUVASTATIN COMPARED WITH ROSUVASTATIN ON LOW-DENSITY LIPOPROTEIN CHOLESTEROL IN PATIENTS WITH HYPERCHOLESTEROLAEMIA
- Registry ID
- D7961C00001
- Source registry
- HEALTH_CANADA
- Status
- Pending
- Phase
- PHASE3
- Study type
- INTERVENTIONAL
- Sponsor
- ASTRAZENECA CANADA INC
- Last update
- 2026-07-17
Conditions
Related clinical trials
- A PHASE 3, OPEN-LABEL EXTENSION STUDY TO EVALUATE THE SAFETY AND EFFICACY OF
MK-0616 IN ADULTS WITH HYPERCHOLESTEROLEMIA
- "A MULTI-COUNTRY, MULTICENTER, SINGLE-ARM, OPEN-LABEL STUDY TO DOCUMENT THE SAFETY, TOLERABLITY AND EFFECT OF ALIROCUMAB ON ATHEROGENIC LIPOPROTEINS IN HIGH CARDIO-VASCULAR RISK PATIENTS WITH SEVERE HYPERCHOLESTEROLEMIA NOT ADEQUATELY CONTROLLED WITH CONVENTIONAL LIPID-MODIFYING THERAPIES."
- A DOUBLE-BLIND, RANDOMIZED, MULTICENTER STUDY TO EVALUATE THE SAFETY AND EFFICACY OF AMG 145, COMPARED WITH EZETIMIBE, IN HYPERCHOLESTEROLEMIC SUBJECTS UNABLE TO TOLERATE AN EFFECTIVE DOSE OF A HMG-COA REDUCTASE INHIBITOR DUE TO MUSCLE RELATED SIDE EFFECTS
- "A MULTI-CENTER, RANDOMIZED STUDY IN SUBJECTS WITH PRIMARY HYPERCHOLESTEROLEMIA OR MIXED DYSLIPDEMIA TO ASSESS SUBJECTS' ABILITY TO ADMINISTER A FULL DOSE OF AMG 145 IN HOME-USE, USING EITHER A 3.5ML PERSONAL INJECTOR OR A PREFILLED AUTOINJECTOR/PEN."
View on source registry