Hyperion Therapeutics (FRA:0HY) Total Liabilities : €50.7 Mil (As of Mar. 2015)

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What is Hyperion Therapeutics Total Liabilities?

Hyperion Therapeutics's Total Liabilities for the quarter that ended in Mar. 2015 was €50.7 Mil.

Hyperion Therapeutics's quarterly Total Liabilities declined from Sep. 2014 (€39.81 Mil) to Dec. 2014 (€39.63 Mil) but then increased from Dec. 2014 (€39.63 Mil) to Mar. 2015 (€50.68 Mil).

Hyperion Therapeutics's annual Total Liabilities increased from Dec. 2012 (€12.81 Mil) to Dec. 2013 (€16.67 Mil) and increased from Dec. 2013 (€16.67 Mil) to Dec. 2014 (€39.63 Mil).

Hyperion Therapeutics Total Liabilities Historical Data

The historical data trend for Hyperion Therapeutics's Total Liabilities can be seen below:

* For Operating Data section: All numbers are indicated by the unit behind each term and all currency related amount are in USD.
* For other sections: All numbers are in millions except for per share data, ratio, and percentage. All currency related amount are indicated in the company's associated stock exchange currency.

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Hyperion Therapeutics Total Liabilities Chart

Hyperion Therapeutics Annual Data

Trend

Dec10

Dec11

Dec12

Dec13

Dec14

Total Liabilities

68.59

12.81

16.67

39.63

Hyperion Therapeutics Quarterly Data
	Dec10	Mar11	Jun11	Sep11	Dec11	Mar12	Jun12	Sep12	Dec12	Mar13	Jun13	Sep13	Dec13	Mar14	Jun14	Sep14	Dec14	Mar15
Total Liabilities	Get a 7-Day Free Trial													15.56	111.44	39.81	39.63	50.68

Hyperion Therapeutics Total Liabilities Calculation

Total Liabilities are the liabilities that the company has to pay others. It is a part of the balance sheet of a company that shareholders do not own, and would be obligated to pay back if the company liquidated.

Hyperion Therapeutics's Total Liabilities for the fiscal year that ended in Dec. 2014 is calculated as

Total Liabilities	=	Total Current Liabilities	+	Total Noncurrent Liabilities
	=	Total Current Liabilities	+	(Long-Term Debt & Capital Lease Obligation	+	Other Long-Term Liabilities
	=	24.656	+	(14.699	+	-0.00099999999998435
	+	NonCurrent Deferred Liabilities	+	PensionAndRetirementBenefit)
	+	0.274	+	0)
	=	39.6

Total Liabilities	=	Total Assets (A: Dec. 2014 )	-	Total Equity (A: Dec. 2014 )
	=	146.317	-	106.689
	=	39.6

Hyperion Therapeutics's Total Liabilities for the quarter that ended in Mar. 2015 is calculated as

Total Liabilities	=	Total Current Liabilities	+	Total Noncurrent Liabilities
	=	Total Current Liabilities	+	(Long-Term Debt & Capital Lease Obligation	+	Other Long-Term Liabilities
	=	34.984	+	(15.397	+	-1.4044321261508E-14
	+	NonCurrent Deferred Liabilities	+	PensionAndRetirementBenefit)
	+	0.301	+	0)
	=	50.7

Total Liabilities	=	Total Assets (Q: Mar. 2015 )	-	Total Equity (Q: Mar. 2015 )
	=	180.208	-	129.526
	=	50.7

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Hyperion Therapeutics (FRA:0HY) Business Description

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Traded in Other Exchanges

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Address

Website

http://www.hyperiontx.com

Hyperion Therapeutics Inc., was incorporated in Delaware on November 1, 2006. The Company completed its initial public offering on July 2012. It is a commercial biopharmaceutical company, engaged in the development and commercialization of novel therapeutics to treat disorders in the areas of orphan diseases and hepatology. Its products, RAVICTI (glycerol phenylbutyrate) Oral liquid, BUPHENYL and AMMONAPS (sodium phenylbutyrate) Tablets and Powder, are designed to lower ammonia in the blood. The Company has developed RAVICTI to treat urea cycle disorders including 7 of the 8 prevalent UCD subtypes, and is developing glycerol phenylbutyrate, the active pharmaceutical ingredient in RAVICTI, to treat hepatic encephalopathy. RAVICTI is indicated for use as a nitrogen-binding agent for chronic management of adult and pediatric patients above 2 years of age with urea cycle disorders who cannot be managed by dietary protein restriction and/or amino acid supplementation alone. It distributes RAVICTI through two specialty pharmacies with a single dedicated call center responsible for interfacing with patients, physicians and payors. BUPHENYL is indicated in all patients with neonatal-onset deficiency (complete enzymatic deficiency, presenting within the first 28 days of life). It is also indicated in patients with late-onset disease (partial enzymatic deficiency, presenting after the first month of life) who have a history of hyperammonemic encephalopathy. The Company faces competition from established pharmaceutical and biotechnology companies, as well as from academic institutions, government agencies and private and public research institutions, among others, which may in the future develop products to treat UCD or HE. The Company is subject to numerous federal, state and local laws relating to such matters as safe working conditions, manufacturing practices, environmental protection, fire hazard control, and disposal of hazardous or potentially hazardous substances.

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