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Tim Mayleben on clinical data

From Esperion CEO on safety of new cholesterol drug · · CNBCTelevision

“We have roughly 4,000 patients enrolled who have taken our drug, most for more than a year, and when we've put all of that data together our drug looks as good as the sugar pill or placebo in those analyses.”

Tim Mayleben
Former CEO, Esperion Therapeutics
Controversial clinical datatrial sizesafety signal

On , Tim Mayleben, Former CEO at Esperion Therapeutics, spoke about clinical data during Esperion CEO on safety of new cholesterol drug on CNBCTelevision.

Esperion CEO on safety of new cholesterol drug
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Esperion CEO on safety of new cholesterol drug
CNBCTelevision
Watch on YouTube at 3:13
CNBC's Meg Tirrell reports on Esperion shares heading higher on its new cholesterol drug. Esperion CEO and President Tim Mayleben joins 'Power Lunch' to discuss the new drug and drug pricing. » Subscribe to CNBC: http://cnb.cx/SubscribeCNBC About CNBC: From 'Wall Street' to 'Main Street' to award winning original documentaries and Reality TV series, CNBC has you covered. Experience special sneak peeks of your favorite shows, exclusive video and more. Connect with CNBC News Online Get the latest news: http://www.cnbc.com/ Find CNBC News on Facebook: http://cnb.cx/LikeCNBC Follow CNBC News on Twitter: http://cnb.cx/FollowCNBC Follow CNBC News on Google+: http://cnb.cx/PlusCNBC Follow CNBC News on Instagram: http://cnb.cx/InstagramCNBC #CNBC
Tim Mayleben

About Tim Mayleben

Former CEO · Esperion Therapeutics

In October 2018, Tim Mayleben, then CEO of Esperion Therapeutics, discussed the company's experimental cholesterol drug bempedoic acid on CNBC. He stated that the drug is an oral, once-daily pill that demonstrated a reduction in LDL cholesterol by about 20% on top of statins and was safe and well tolerated. Mayleben said the drug is intended for patients taking the maximum tolerated dose of a statin who still need additional LDL lowering, including those who have had cardiac events. He noted that the drug did not appear to cause the same muscle aches associated with statins. Mayleben also said that in clinical studies involving roughly 4,000 patients, the drug's safety profile looked comparable to a placebo. He expected FDA approval and a market launch in 2020. Regarding business strategy, Mayleben said the company was open to a worldwide or regional partner for commercialization, as well as other strategic considerations, with the goal of benefiting shareholders. He added that his own wife, who has genetic cholesterol issues and cannot take statins, would be a candidate for the drug.

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