Study to Evaluate the Efficacy and Safety of Lomitapide in Japanese Patients with Homozygous Familial Hypercholesterolemia (HoFH) on Concurrent Lipid-Lowering Therapy.
This is a Phase 3, single-arm, open-label, multicenter clinical trial to evaluate both the efficacy and long-term safety of lomitapide in Japanese patients with HoFH receiving maximally-tolerated, stable lipid-lowering therapy. This study is comprised of a run-in period, a primary 26-week Efficacy Phase, and a 30-week Safety Phase.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Unnamed facility
Kurume-shi, Fukuoka, Japan
Unnamed facility
Kanazawa, Ishikawa-ken, Japan
Unnamed facility
Osakashi, Osaka, Japan
Unnamed facility
Suita-shi, Osaka, Japan
Unnamed facility
Percent Change in LDL-C
Mean percent change from baseline
Time frame: Baseline to Week 26
Change in Total Cholesterol
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in Apo B
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in Triglycerides
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in Non-HDL-C
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in VLDL-C
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in Lp(a)
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in HDL-C
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in Apo AI
Mean percent change from baseline
Time frame: Baseline to Week 56
Change in LDL-C
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Tokorozawa, Saitama, Japan
Unnamed facility
Bunkyo-ku, Tokyo, Japan
Mean percent change from baseline
Time frame: Baseline to Week 56