Adaptive Biotechnologies (FRA:1HM) Cash from Discontinued Operating Activities : €0.0 Mil (TTM As of Mar. 2024)

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What is Adaptive Biotechnologies Cash from Discontinued Operating Activities?

Cash from Discontinued Operating Activities is net cash from all of the entity's discontinued operating activities.

Adaptive Biotechnologies's Cash from Discontinued Operating Activities for the three months ended in Mar. 2024 was €0.0 Mil. It means Adaptive Biotechnologies received €0.0 Mil from discontinued investing activities. Adaptive Biotechnologies's Cash from Discontinued Operating Activities for the trailing twelve months (TTM) ended in Mar. 2024 was €0.0 Mil.

Adaptive Biotechnologies Cash from Discontinued Operating Activities Historical Data

The historical data trend for Adaptive Biotechnologies's Cash from Discontinued Operating Activities 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 Cash from Discontinued Operating Activities Chart

Adaptive Biotechnologies Annual Data

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Cash from Discontinued Operating Activities

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Adaptive Biotechnologies Quarterly Data
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Adaptive Biotechnologies Cash from Discontinued Operating Activities Calculation

Cash from Discontinued Operating Activities is net cash from all of the entity's discontinued operating activities.

Cash from Discontinued Operating Activities for the trailing twelve months (TTM) ended in Mar. 2024 adds up the quarterly data reported by the company within the most recent 12 months, which was €0.0 Mil.

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Adaptive Biotechnologies (FRA:1HM) Business Description

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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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