Clinical trial
A Safety, Pharmacokinetic, and Pharmacodynamic Assessment of 28-Day Oral Dosing of RVX000222 in Healthy Subjects and Subjects With Low High Density Lipoprotein (HDL)
NCT00768274 is registered in ClinicalTrials.gov with Resverlogix Corp as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Safety, Pharmacokinetic, and Pharmacodynamic Assessment of 28-Day Oral Dosing of RVX000222 in Healthy Subjects and Subjects With Low High Density Lipoprotein (HDL)
- Lead sponsor
- Resverlogix Corp
- Phase
- Phase 1/2
- Overall status
- Completed
- Start date
- September 30, 2008
- Completion date
- August 31, 2009
- Enrollment
- 72 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
acute coronary syndrome, atherosclerosis, cardiovascular disease, dyslipidemia