Nabriva Therapeutics (STU:NTY) Change In Prepaid Assets : €0.00 Mil (TTM As of Jun. 2023)

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What is Nabriva Therapeutics Change In Prepaid Assets?

Nabriva Therapeutics's Change In Prepaid Assets for the quarter that ended in Jun. 2023 was €0.00 Mil. It means Nabriva Therapeutics's Prepaid Assets stayed the same from Mar. 2023 to Jun. 2023 .

Nabriva Therapeutics's Change In Prepaid Assets for the fiscal year that ended in Dec. 2022 was €0.00 Mil. It means Nabriva Therapeutics's Prepaid Assets stayed the same from Dec. 2021 to Dec. 2022 .

Nabriva Therapeutics Change In Prepaid Assets Historical Data

The historical data trend for Nabriva Therapeutics's Change In Prepaid Assets 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 Change In Prepaid Assets Chart

Nabriva Therapeutics Annual Data

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Change In Prepaid Assets

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Nabriva Therapeutics Quarterly Data
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Nabriva Therapeutics Change In Prepaid Assets Calculation

Change In Prepaid Assets is any increase or decrease between periods of the prepaid assets.

Change In Prepaid Assets 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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Address

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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