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Hyperion Therapeutics Secures $40 Million In Series B Round
Date:9/5/2007

forward to working in partnership with Hyperion on shared goals to improve the lives of UCD patients and their families."

Hyperion recently announced their strategic collaboration with Medicis (NYSE: MRX) through which the Company will immediately begin promotion of the only currently FDA approved drugs for the treatment of UCD (AMMONUL and BUPHENYL) and continue developing AMMONUL for acute hepatic encephalopathy (HE) and a compound referred to as GT4P for chronic UCD and HE.

In addition to the Series B financing, Hyperion named the following board members: James Healy of Sofinnova Ventures, Mike Raab of NEA, Bijan Salehizadeh of Highland Capital Partners, and Don Santel, former CEO of CoTherix, Inc.

About Hyperion Therapeutics

Hyperion Therapeutics is a specialty therapeutics company focused on becoming a global leader in gastrointestinal (GI) and hepatology therapeutic programs and products that address underserved patient populations or unmet medical needs to improve patient care. The company has assembled a seasoned executive team with extensive industry experience developing and commercializing specialty pharmaceutical products. Hyperion is headquartered in South San Francisco, CA. For additional information, visit: http://www.hyperiontx.com.

AMMONUL and BUPHENYL are registered trademarks of Ucyclyd Pharma, Inc.

Full prescribing information for AMMONUL(R) and BUPHENYL(R) are available at http://www.Ammonul.com and http://www.Buphenyl.com, respectively, or by contacting Hyperion Therapeutics, Inc.


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SOURCE Hyperion Therapeutics, Inc.
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