Nabriva Therapeutics (STU:NTY) Short-Term Debt : €0.18 Mil (As of Jun. 2023)

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What is Nabriva Therapeutics Short-Term Debt?

Nabriva Therapeutics's Short-Term Debt for the quarter that ended in Jun. 2023 was €0.18 Mil.

Nabriva Therapeutics's quarterly Short-Term Debt declined from Dec. 2022 (€4.56 Mil) to Mar. 2023 (€0.18 Mil) and declined from Mar. 2023 (€0.18 Mil) to Jun. 2023 (€0.18 Mil).

Nabriva Therapeutics's annual Short-Term Debt increased from Dec. 2020 (€1.68 Mil) to Dec. 2021 (€3.33 Mil) and increased from Dec. 2021 (€3.33 Mil) to Dec. 2022 (€4.56 Mil).

Nabriva Therapeutics Short-Term Debt Historical Data

The historical data trend for Nabriva Therapeutics's Short-Term Debt 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 Short-Term Debt Chart

Nabriva Therapeutics Annual Data

Trend

Dec13

Dec14

Dec15

Dec16

Dec17

Dec18

Dec19

Dec20

Dec21

Dec22

Short-Term Debt

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1.68

3.33

4.56

Nabriva Therapeutics Quarterly Data
	Sep18	Dec18	Mar19	Jun19	Sep19	Dec19	Mar20	Jun20	Sep20	Dec20	Mar21	Jun21	Sep21	Dec21	Mar22	Jun22	Sep22	Dec22	Mar23	Jun23
Short-Term Debt	Get a 7-Day Free Trial															6.27	5.79	4.56	0.18	0.18

Nabriva Therapeutics Short-Term Debt Explanation

Short-Term Debt represents the total amount of Long-Term Debt such as bank loans and commercial paper, which is due within one year.

Nabriva Therapeutics Short-Term Debt Related Terms

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Nabriva Therapeutics (STU:NTY) Business Description

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NBRVF:USA

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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