Adaptive Biotechnologies (FRA:1HM) Current Deferred Taxes Liabilities : €0.0 Mil (As of Jun. 2024)

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What is Adaptive Biotechnologies Current Deferred Taxes Liabilities?

Current Deferred Taxes Liabilities represent future tax liabilities, resulting from temporary differences between book (accounting) value of assets and liabilities and their tax value, or timing differences between the recognition of gains and losses in financial statements and their recognition in a tax computation. Deferred tax liabilities generally arise where tax relief is provided in advance of an accounting expense, or income is accrued but not taxed until received.

Adaptive Biotechnologies's current deferred tax liabilities for the quarter that ended in Jun. 2024 was €0.0 Mil.

Adaptive Biotechnologies Current Deferred Taxes Liabilities Historical Data

The historical data trend for Adaptive Biotechnologies's Current Deferred Taxes 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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Adaptive Biotechnologies Current Deferred Taxes Liabilities Chart

Adaptive Biotechnologies Annual Data

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Current Deferred Taxes Liabilities

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Adaptive Biotechnologies Quarterly Data
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Adaptive Biotechnologies Business Description

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GURUFOCUS.COM » STOCK LIST » Healthcare » Biotechnology » Adaptive Biotechnologies Corp (FRA:1HM) » Definitions » Current Deferred Taxes Liabilities

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ADPT:USA 1HM:Germany

Address

1165 Eastlake Avenue East, Seattle, WA, USA, 98109

Website

https://www.adaptivebiotech.com

Adaptive Biotechnologies Corp is a company advancing the field of immune-driven medicine by harnessing the inherent biology of the adaptive immune system to transform the diagnosis and treatment of disease. Its clinical diagnostic product, clonoSEQ, is test authorized by the FDA for the detection and monitoring of minimal residual disease (MRD) in patients with multiple myeloma (MM), B cell acute lymphoblastic leukemia (ALL) and chronic lymphocytic leukemia (CLL) and is also available as a CLIA-validated laboratory developed test (LDT) for patients with other lymphoid cancers, including diffuse large B-cell lymphoma (DLBCL).

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