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Homology Medicines (STU:35H) Other Current Liabilities : €5.28 Mil (As of Dec. 2023)


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What is Homology Medicines Other Current Liabilities?

Homology Medicines's other current liabilities for the quarter that ended in Dec. 2023 was €5.28 Mil.

Homology Medicines's quarterly other current liabilities increased from Jun. 2023 (€3.33 Mil) to Sep. 2023 (€6.24 Mil) but then declined from Sep. 2023 (€6.24 Mil) to Dec. 2023 (€5.28 Mil).

Homology Medicines's annual other current liabilities declined from Dec. 2021 (€6.91 Mil) to Dec. 2022 (€5.62 Mil) and declined from Dec. 2022 (€5.62 Mil) to Dec. 2023 (€5.28 Mil).


Homology Medicines Other Current Liabilities Historical Data

The historical data trend for Homology Medicines's Other Current 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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Homology Medicines Other Current Liabilities Chart

Homology Medicines Annual Data
Trend Dec16 Dec17 Dec18 Dec19 Dec20 Dec21 Dec22 Dec23
Other Current Liabilities
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Homology Medicines Quarterly Data
Mar19 Jun19 Sep19 Dec19 Mar20 Jun20 Sep20 Dec20 Mar21 Jun21 Sep21 Dec21 Mar22 Jun22 Sep22 Dec22 Mar23 Jun23 Sep23 Dec23
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Homology Medicines Other Current Liabilities Calculation

The liability a company needs to pay in the next 12 months, but not assigned to Accounts Payable or Debt. For instance, Wal-Mart (WMT) has accrued wages, salaries, valuation, bonuses, insurance liabilities, accrued tax etc. These are all included in other current liabilities.


Homology Medicines Other Current Liabilities Related Terms

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Homology Medicines (STU:35H) Business Description

Traded in Other Exchanges
Address
One Patriots Park, Bedford, MA, USA, 01730
Homology Medicines Inc is a United States-based genetic medicines company dedicated to transforming the lives of patients suffering from rare genetic diseases with significant unmet medical needs by curing the underlying cause of the disease. Its proprietary platform is designed to utilize its human hematopoietic stem cell derived adeno-associated virus vectors (AAVHSCs) to deliver genetic medicines in vivo either through a gene therapy or nuclease-free gene editing modality across a range of genetic disorders.

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