Nabriva Therapeutics (STU:NTY) Cash Flow from Discontinued Operations : €0.00 Mil (TTM As of Jun. 2023)

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What is Nabriva Therapeutics Cash Flow from Discontinued Operations?

Cash flow from discontinued operations is the cash received by a company that comes from the sale of part of business.

Nabriva Therapeutics's cash flow from discontinued operations for the three months ended in Jun. 2023 was €0.00 Mil. It means Nabriva Therapeutics received €0.00 Mil from the sale of part of business quarterly. Nabriva Therapeutics's cash flow from discontinued operations for the trailing twelve months (TTM) ended in Jun. 2023 was €0.00 Mil.

Nabriva Therapeutics Cash Flow from Discontinued Operations Historical Data

The historical data trend for Nabriva Therapeutics's Cash Flow from Discontinued Operations 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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Nabriva Therapeutics Cash Flow from Discontinued Operations Chart

Nabriva Therapeutics Annual Data

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Cash Flow from Discontinued Operations

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Nabriva Therapeutics Quarterly Data
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Nabriva Therapeutics Cash Flow from Discontinued Operations Calculation

Cash received by a company that comes from the sale of part of business.

Cash Flow from Discontinued Operations for the trailing twelve months (TTM) ended in Jun. 2023 adds up the quarterly data reported by the company within the most recent 12 months, which was €0.00 Mil.

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Nabriva Therapeutics (STU:NTY) Business Description

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Alexandra House, Office 225/227, The Sweepstakes, Dublin, IRL, 4

Website

https://www.nabriva.com

Nabriva Therapeutics PLC is a clinical stage biopharmaceutical company. Nabriva is engaged in the research and development of novel anti-infective agents to treat serious infections, with a focus on the pleuromutilin class of antibiotics. The company has developed a product candidate, XENLETA, a semi-synthetic pleuromutilin antibiotic that is the first in its class for oral and IV administration in humans. XENLETA is designed to inhibit the synthesis of a specific protein on the bacterial ribosome. It operates in one reportable segment, which comprises the research and development of novel anti-infective agents to treat serious infections. The firm has commercial rights to two approved products, SIVEXTRO and XENLETA, as well as one development product candidate, CONTEPO.

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