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Hyperion Therapeutics Announces Enrollment of First Patient in Phase 2 Clinical Trial in Patients With Hepatic Encephalopathy
Date:2/25/2008

ministering to patients with hepatic or renal insufficiency. AMMONUL may cause nausea and vomiting. An antiemetic may be administered during infusion. See the prescribing information for a complete listing of warnings, precautions, and drug interactions.

About Hyperion Therapeutics

Hyperion Therapeutics is a fully-integrated specialty therapeutics company focused on becoming a global leader in hepatology and gastrointestinal (GI) therapeutic programs and products that address orphan or underserved patient populations with unmet medical needs. 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(R) is exclusively licensed from Ucyclyd Pharma, Inc. No milestones are payable upon initiation of the trial described in this release.

AMMONUL(R) is a registered trademark of Ucyclyd Pharma, Inc.

Full Prescribing Information for AMMONUL(R) is available at http://www.Ammonul.com or by contacting Hyperion Therapeutics, Inc.


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SOURCE Hyperion Therapeutics, Inc.
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