Maxygen, (FRA:MYN) Other Current Liabilities : €0.00 Mil (As of Mar. 2013)

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What is Maxygen, Other Current Liabilities?

Maxygen,'s other current liabilities for the quarter that ended in Mar. 2013 was €0.00 Mil.

Maxygen,'s annual other current liabilities declined from Dec. 2010 (€0.00 Mil) to Dec. 2011 (€0.00 Mil) but then stayed the same from Dec. 2011 (€0.00 Mil) to Dec. 2012 (€0.00 Mil).

Maxygen, Other Current Liabilities Historical Data

The historical data trend for Maxygen,'s Other Current 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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Maxygen, Other Current Liabilities Chart

Maxygen, Annual Data

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Other Current Liabilities

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Maxygen, Quarterly Data
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Other Current Liabilities	Get a 7-Day Free Trial															-	-	-	-	-

Maxygen, Other Current Liabilities Calculation

The liability a company needs to pay in the next 12 months, but not assigned to Accounts Payable or Debt. For instance, Wal-Mart (WMT) has accrued wages, salaries, valuation, bonuses, insurance liabilities, accrued tax etc. These are all included in other current liabilities.

Maxygen, Other Current Liabilities Related Terms

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Maxygen, (FRA:MYN) Business Description

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GURUFOCUS.COM » STOCK LIST » Healthcare » Biotechnology » Maxygen, Inc. (FRA:MYN) » Definitions » Other Current Liabilities

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Maxygen, Inc., is incorporated in Delaware. It is a biotechnology company. It discovers and develops improved next-generation protein pharmaceuticals for the treatment of disease and serious medical conditions. The Company's MAXY-G34 product candidate has been designed to be an improved next-generation pegylated, G-CSF for the treatment of chemotherapy-induced neutropenia. G-CSF is a natural protein that functions by stimulating the body's bone marrow to produce more white blood cells. The Company completed a Phase IIa clinical trial for its MAXY-G34 product candidate for the treatment of chemotherapy-induced neutropenia in breast cancer patients in which MAXY-G34 was safe and effective in reducing chemotherapy-induced neutropenia with no serious adverse events, drug-related grade 3 or 4 adverse events or immunogenicity reported in any patient receiving MAXY-G34. Adverse events were consistent with known side effects of G-CSF molecules. The Company is subject to regulation by the FDA and comparable regulatory agencies in foreign countries with respect to any development and commercialization of its MAXY-G34 product candidate or any other products it may acquire in the future.