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Titan Pharmaceuticals (FRA:TN70) Current Deferred Taxes Liabilities : €0.00 Mil (As of Mar. 2024)


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What is Titan Pharmaceuticals Current Deferred Taxes Liabilities?

Current Deferred Taxes Liabilities represent future tax liabilities, resulting from temporary differences between book (accounting) value of assets and liabilities and their tax value, or timing differences between the recognition of gains and losses in financial statements and their recognition in a tax computation. Deferred tax liabilities generally arise where tax relief is provided in advance of an accounting expense, or income is accrued but not taxed until received.

Titan Pharmaceuticals's current deferred tax liabilities for the quarter that ended in Mar. 2024 was €0.00 Mil.

Titan Pharmaceuticals Current Deferred Taxes Liabilities Historical Data

The historical data trend for Titan Pharmaceuticals's Current Deferred Taxes Liabilities 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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Titan Pharmaceuticals Current Deferred Taxes Liabilities Chart

Titan Pharmaceuticals Annual Data
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Current Deferred Taxes Liabilities
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Titan Pharmaceuticals Quarterly Data
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Titan Pharmaceuticals (FRA:TN70) Business Description

Industry
Traded in Other Exchanges
Address
400 Oyster Point Boulevard, Suite 505, South San Francisco, CA, USA, 94080
Titan Pharmaceuticals Inc is a pharmaceutical company developing therapeutics utilizing its proprietary long-term drug delivery platform, ProNeura, for the treatment of select chronic diseases for which steady state delivery of a drug provides efficacy and/or safety benefit. ProNeura consists of a small, solid implant made from a mixture of ethylene-vinyl acetate, or EVA, and a drug substance. Its first product based on ProNeura technology was the Probuphine (buprenorphine) implant, which was approved in the United States, Canada and the European Union, for the maintenance treatment of opioid use disorder in clinically stable patients taking 8 mg or less a day of oral buprenorphine.

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