Bruce Hammock to Speak on Pioneeering Inflammation Research

Nov. 7, 2007

Bruce Hammock

Bruce Hammock

DAVIS Bruce Hammock, distinguished professor of entomology with the Department of Entomology and the Cancer Research Center at the University of California, Davis,  will speak on his pioneering inflammation research at an hourlong talk at 12:10 a.m., Friday, Nov. 9 in the Genome Center. His lecture is part of the Emerging Challenges in Microbiology and Immunology Series.

Hammock’s talk, “The Soluble Epoxide Hydrolase as a New Target to Treat Inflammation,”  takes place in Room 1005 of the Genome Center, located on West Health Sciences Drive.

Epoxide hydrolase inhibitors are novel first-in-class drugs that block an immune system protein known to play a role in inflammatory diseases of the heart, kidneys and other organs. .“The compounds are not only more potent than nonsteroidial anti-inflammatory drugs; they synergize with them and reduce side effects.”

 “The research offers a powerful new avenue for drug development,” said Hammock, whose inflammation research sprang from studies on fundamental insect development.

The lecture is timely in that the first of these compounds just entered human clinical trials. “It is rare,” said Hammock, “that a compound made and tested in an academic lab makes it all the way to clinical trials (through Arête  Therapeutics).” See below

Hammock directs the UC Davis Superfund Basic Research Program of the National Institute of Environmental Health Sciences (NIEHS). The UC Davis Genome Center integrates experimental and computational approaches to address key problems at the forefront of genomics.

Map to Genome Center

Arête Therapeutics Initiates Phase 1 Clinical Trial For AR9281 as a First-in-Class Antihypertensive Agent

HAYWARD, Calif. (Nov. 1 /PRNewswire) — Arête Therapeutics Inc. today announced the initiation of a phase 1 clinical trial for its lead compound, AR9281, for the treatment of hypertension.  AR9281 is a "first-in-class," orally-active inhibitor of soluble epoxide hydrolase (s-EH), a novel target for the treatment of hypertension.  The trial will enroll up to 32 healthy adult volunteers and will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics for single ascending doses of AR9281.

"AR9281 inhibits s-EH, an enzyme that plays a key role in the cytochrome P450 pathway of arachidonic acid metabolism, and offers a unique mechanism of action as an antihypertensive agent," said Dinesh V. Patel, Ph.D., president and chief executive officer of ArêteTherapeutics Inc. "We believe this first-in-class compound has great potential to be a unique 'antihypertensive-plus' drug that not only lowers blood pressure but also offers end organ protection of the heart and kidney, and protection against vascular inflammation."

"The preclinical safety and efficacy profile of AR9281 is very encouraging and provided a solid basis for the initiation of the clinical development phase of this new compound class," commented Randall Whitcomb, M.D., chief medical officer of Arête Therapeutics Inc.  "We look forward to reporting results from the initial phase 1 clinical trial in 2008."

Arête Therapeutics' phase 1 single ascending dose, placebo-controlled clinical trial in healthy volunteers will obtain initial safety and tolerance information as well as detailed blood pressure measurements. Levels of s-EH specific biomarkers will be analyzed together with typical inflammatory markers as part of the pharmacodynamic assessment. Following successful completion of the single dose study, Arête plans to initiate a multiple dose phase 1 study, a food effect study, and studies in special populations. 

About AR9281
AR9281 is a novel small molecule inhibitor of soluble epoxide hydrolase (s-EH), an enzyme which plays a key role in arachidonic acid metabolism, and has the potential to be a first-in-class antihypertensive agent with end organ protection and anti-inflammatory properties.  AR9281 has shown activity in multiple animal models of hypertension and vascular inflammation.  In addition, Arête has evaluated AR9281 in numerous in vitro and in vivo assays for potency, selectivity, efficacy, ADME, toxicity and safety with very favorable results.

Over the past decade, various academic institutions have proven the therapeutic utility of s-EH inhibitors in multiple models of hypertension, demonstrating that they lower elevated blood pressure, provide a protective effect on the kidney, heart and brain, and possess anti-inflammatory properties.  Based on positive preclinical data, Arête is pursuing additional studies to explore the impact of s-EH inhibition on inflammation and the metabolic syndrome.

About Hypertension
 Hypertension impacts more than 50 million people in the US and over 1 billion people worldwide. The risk of hypertension increases with age and is likely to represent one of the single most common chronic diseases in an aging population.  The relationship between high blood pressure and the risk of cardiovascular disease is continuous, consistent, and independent of all other risk factors.  The aggressive management of elevated blood pressure has consistently been shown to reduce the rates of stroke, heart attack, and heart failure.  Current therapies are often changed or discontinued within the first 6 months in most medical practices, likely reflecting a combination of adverse drug effects, poor efficacy, and a lack of understanding of target organ damage. 

About Arête Therapeutics Inc.
Arête Therapeutics Inc. is a privately held pharmaceutical company discovering and developing first-in-class small molecule drugs directed at soluble epoxide hydrolase (s-EH), a novel target for cardiovascular, metabolic and inflammatory diseases. By targeting s-EH which plays a key role in the arachidonic acid pathway, the company is addressing the very large market need for a unique anti-hypertensive drug with renal sparing, cardio-protective and anti-inflammatory properties.  Arête has discovered and developed a series of proprietary and chemically diverse molecules with preclinical efficacy in various animal models of hypertension, metabolic syndrome, and inflammation, and is conducting a phase 1 clinical trial with its first-in-class antihypertensive drug AR9281. The company has raised a total of $51 million in Series A financing led by Frazier Healthcare Ventures, Alta Partners), Three Arch Partners, Burrill & Company and Altitude Life Science Ventures). See more information on Arête Therapeutics Web site.


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--Kathy Keatley Garvey
Communications specialist
UC Davis Department of Entomology
(530) 754-6894