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Last $105.24 USD
Change Today +12.64 / 13.65%
Volume 2.6M
ESPR On Other Exchanges
As of 8:10 PM 04/1/15 All times are local (Market data is delayed by at least 15 minutes).

esperion therapeutics inc (ESPR) Snapshot

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Day High
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52 Week High
03/19/15 - $118.95
52 Week Low
04/15/14 - $12.75
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Average Volume 10 Days
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esperion therapeutics inc (ESPR) Details

Esperion Therapeutics, Inc., a biopharmaceutical company, focuses on the research, development, and commercialization of oral and low-density lipoprotein cholesterol lowering therapies for the treatment of patients with hypercholesterolemia and other cardiometabolic risk markers. Its products include ETC-1002, an oral molecule therapy that is in Phase 2b clinical trials to treat patients with hypercholesterolemia, as well as to lower levels of LDL-cholesterol, and avoid various side effects associated with LDL-cholesterol lowering therapies. The company’s products also comprise 4WF, a synthetic apoA-I therapy for treating patients with acute coronary syndrome has completed Phase 2a clinical studies; and ESP41091, which is in pre-clinical trials for lipid metabolism and body weight reduction. Esperion Therapeutics, Inc. is headquartered in Ann Arbor, Michigan.

21 Employees
Last Reported Date: 03/10/15

esperion therapeutics inc (ESPR) Top Compensated Officers

Chief Executive Officer, President, Principal...
Total Annual Compensation: $400.0K
Senior Advisor to Chief Executive Officer
Total Annual Compensation: $335.0K
Executive Chairman and Chief Scientific Offic...
Total Annual Compensation: $375.0K
Compensation as of Fiscal Year 2013.

esperion therapeutics inc (ESPR) Key Developments

Esperion Therapeutics, Inc. - Special Call

To discuss positive top-line results from ETC-1002-009, a Phase 2b study evaluating the efficacy and safety of ETC-1002 (bempedoic acid) compared with placebo in patients with hypercholesterolemia on stable statin therapy.

Esperion Therapeutics, Inc. Announces Positive Top-Line Results from ETC-1002-009, a Phase 2b study

Esperion Therapeutics, Inc. announced positive top-line results from ETC-1002-009, a Phase 2b study evaluating the efficacy and safety of ETC-1002 (bempedoic acid) compared with placebo in patients with hypercholesterolemia on stable statin therapy. Top-line results showed the 12-week study met its primary endpoint of greater LDL-cholesterol lowering from baseline with ETC-1002 compared with placebo. ETC-1002-treated patients achieved 17 and 24% incremental reductions in LDL-cholesterol at doses of 120 mg and 180 mg, respectively, compared with patients on stable statin therapy alone. These reductions were significantly different from placebo, occurred within the first two weeks of initiating therapy, and continued throughout the treatment period. Consistent with prior studies, ETC-1002 demonstrated reductions of up to 30% in high-sensitivity C-reactive protein (hsCRP), an important marker of inflammation in coronary disease. ETC-1002-treated patients achieved LDL-cholesterol lowering of up to an additional 24% at 12 weeks compared with 4% in the placebo group. Levels of hsCRP were reduced by up to 30% with ETC-1002. ETC-1002 was safe and well tolerated, with no muscle-related AEs or ETC-1002-related SAEs.

Esperion Therapeutics, Inc. - Special Call

To provide analysis from the study, and a program update on ETC-1002, including the development of a fixed dose combination with ezetimibe


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