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OncoZenge AB (FRA:8LY) Total Tax Payable : €0.00 Mil (As of Sep. 2024)


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What is OncoZenge AB Total Tax Payable?

OncoZenge AB's Total Tax Payable for the quarter that ended in Sep. 2024 was €0.00 Mil.

OncoZenge AB's annual Total Tax Payable increased from Dec. 2021 (€0.00 Mil) to Dec. 2022 (€0.02 Mil) and increased from Dec. 2022 (€0.02 Mil) to Dec. 2023 (€0.03 Mil).


OncoZenge AB Total Tax Payable Historical Data

The historical data trend for OncoZenge AB's Total Tax 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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OncoZenge AB Total Tax Payable Chart

OncoZenge AB Annual Data
Trend Dec20 Dec21 Dec22 Dec23
Total Tax Payable
- - 0.02 0.03

OncoZenge AB Quarterly Data
Dec20 Mar21 Jun21 Sep21 Dec21 Mar22 Jun22 Sep22 Dec22 Mar23 Jun23 Sep23 Dec23 Mar24 Jun24 Sep24
Total Tax Payable Get a 7-Day Free Trial Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only - 0.03 - - -

OncoZenge AB Total Tax Payable Calculation

Total Tax Payable is the taxes liability owed to federal, state, and local tax authorities. It is the carrying value as of the balance sheet date of obligations incurred and payable for statutory income, sales, use, payroll, excise, real, property and other taxes.


OncoZenge AB Total Tax Payable Related Terms

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OncoZenge AB Business Description

Traded in Other Exchanges
Address
Gustavslundsvagen 34, Bromma, SWE, 167 51
OncoZenge AB is a pharmaceutical company that is developing a new treatment for effective pain relief in patients suffering from oral pain caused by radiation therapy and chemotherapy for cancer. In phase 2 patient studies, the company's product candidate BupiZenge displayed pain relief compared with standard therapy. It focuses on implementing a phase development program as a basis for regulatory approvals and product launches.

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