A Phase 2 interventional study of JTT-302 and JTT-302 in Dyslipidemia, sponsored by Akros Pharma Inc.. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2013-02-04.
Sponsored by Akros Pharma Inc. · Phase 2, Interventional, and Treatment
The purpose of this study is to determine the effect of JTT-302 on the increase of High Density Lipoprotein-Cholesterol (HDL-C) levels when administered daily for four weeks in subjects with low HDL-C levels.
1,073 studies on the registry are indexed under Dyslipidemias; 158 are open to participants now.
This study's enrollment of 150 is above the median of 99 across 842 interventional studies indexed under Dyslipidemias.
Browse Dyslipidemias studies →Akros Pharma Inc. is the lead sponsor of 25 studies on the registry; none are open to participants now.
Of its 5 completed or terminated interventional studies of FDA-regulated products, 4 (80%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
JTT-302, 200 mg
Drug: JTT-302
JTT-302, 400 mg
Drug: JTT-302
Matching placebo tablets
Drug: Placebo
JTT-302, 100 mg tablets, 200 mg dose, oral, 30 minutes after the start of the morning meal
JTT-302, 100 mg tablets, 400 mg dose, oral, 30 minutes after the start of the morning meal
Matching placebo tablets, oral, 30 minutes after the start of the morning meal
Percent change from baseline in HDL-C at Week 4
Time frame: 4 weeks
Percent change and change from baseline at week 4 in lipid parameters
Time frame: 4 weeks
Evaluate the safety profile of JTT-302 when administered for 4 weeks
Time frame: 4 weeks
This study is completed, as verified in Jan 2013. You cannot join it, but the record below documents what was studied.
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Akros Pharma Inc.