Nabriva Therapeutics (STU:NTY) Accounts Payable : €12.95 Mil (As of Jun. 2023)

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What is Nabriva Therapeutics Accounts Payable?

Nabriva Therapeutics's Accounts Payable for the quarter that ended in Jun. 2023 was €12.95 Mil.

Nabriva Therapeutics's quarterly Accounts Payable increased from Dec. 2022 (€5.13 Mil) to Mar. 2023 (€6.52 Mil) and increased from Mar. 2023 (€6.52 Mil) to Jun. 2023 (€12.95 Mil).

Nabriva Therapeutics's annual Accounts Payable increased from Dec. 2020 (€2.38 Mil) to Dec. 2021 (€3.87 Mil) and increased from Dec. 2021 (€3.87 Mil) to Dec. 2022 (€5.13 Mil).

Nabriva Therapeutics Accounts Payable Historical Data

The historical data trend for Nabriva Therapeutics's Accounts Payable 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 Accounts Payable Chart

Nabriva Therapeutics Annual Data

Trend

Dec13

Dec14

Dec15

Dec16

Dec17

Dec18

Dec19

Dec20

Dec21

Dec22

Accounts Payable

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2.90

4.21

2.38

3.87

5.13

Nabriva Therapeutics Quarterly Data
	Sep18	Dec18	Mar19	Jun19	Sep19	Dec19	Mar20	Jun20	Sep20	Dec20	Mar21	Jun21	Sep21	Dec21	Mar22	Jun22	Sep22	Dec22	Mar23	Jun23
Accounts Payable	Get a 7-Day Free Trial															1.02	3.93	5.13	6.52	12.95

Nabriva Therapeutics Accounts Payable Calculation

Accounts Payable represents any money that a company owes its suppliers for goods and services purchased on credit and is expected to pay within the next year or operating cycle.

Nabriva Therapeutics Accounts Payable 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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