A Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of AG2304T and AG2304R
- Registration Number
- NCT06717360
- Lead Sponsor
- Ahn-Gook Pharmaceuticals Co.,Ltd
- Brief Summary
A Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of AG2304T and AG2304R in Patients with Primary Hypercholesterolemia
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
- Adults aged 19-80
- Patients with primary hypercholesterolemia
- Those who voluntarily written consent to participate in this clinical trial
Exclusion Criteria
- The subject not meet the specified LDL-C level
- Other exclusions applied
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description AG2304T AG2304T - AG2304R AG2304R -
- Primary Outcome Measures
Name Time Method LDL-C level 8 weeks
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular targets do AG2304T and AG2304R modulate in primary hypercholesterolemia treatment?
How does AG2304T/AG2304R efficacy compare to PCSK9 inhibitors in reducing LDL-C levels?
Which biomarkers predict response to AG2304T/AG2304R in familial hypercholesterolemia patients?
What are the safety profiles and management strategies for AG2304T/AG2304R adverse events?
Are there combination therapies or competitor drugs targeting similar pathways as AG2304T/AG2304R?