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Gyre Therapeutics | 8-K: Gyre Therapeutics Reports Second Quarter 2024 and Year-To-Date Financial Results and Provides Business Update

Gyre Therapeutics | 8-K: Gyre Therapeutics Reports Second Quarter 2024 and Year-To-Date Financial Results and Provides Business Update

Gyre Therapeutics | 8-K:Gyre Therapeutics公佈2024年第二季度和年初至今的財務業績,並提供業務最新情況
美股SEC公告 ·  2024/08/14 02:38

牛牛AI助理已提取核心訊息

On August 13, 2024, Gyre Therapeutics, Inc., a commercial-stage biotechnology company, announced its financial results for the second quarter and first half of the year ended June 30, 2024. The company reported a net income of $4.5 million for the quarter and $14.5 million for the six months, with revenues of $25.2 million and $52.4 million, respectively. These figures represent a decrease in quarterly revenue compared to the previous year, attributed to normalized sales of their anti-fibrosis drug ETUARY following a temporary surge due to COVID-19 in the PRC. Gyre Therapeutics highlighted several business updates, including the NMPA approval of avatrombopag maleate tablets for CLD-associated thrombocytopenia and the IND approval to evaluate F230 for pulmonary arterial hypertension. The company also expects to submit a U.S...Show More
On August 13, 2024, Gyre Therapeutics, Inc., a commercial-stage biotechnology company, announced its financial results for the second quarter and first half of the year ended June 30, 2024. The company reported a net income of $4.5 million for the quarter and $14.5 million for the six months, with revenues of $25.2 million and $52.4 million, respectively. These figures represent a decrease in quarterly revenue compared to the previous year, attributed to normalized sales of their anti-fibrosis drug ETUARY following a temporary surge due to COVID-19 in the PRC. Gyre Therapeutics highlighted several business updates, including the NMPA approval of avatrombopag maleate tablets for CLD-associated thrombocytopenia and the IND approval to evaluate F230 for pulmonary arterial hypertension. The company also expects to submit a U.S. IND for F351 in MASH-associated liver fibrosis by late 2024 and anticipates Phase 3 trial data for CHB-associated liver fibrosis by early 2025. Gyre's cash and cash equivalents totaled $16.1 million as of June 30, 2024. The report also included the appointment of David M. Epstein to the Board of Directors and the company's addition to the Russell 2000 and Russell 3000 Indexes.
2024年8月13日,商業化階段的生物技術公司Gyre Therapeutics公司公佈了截至2024年6月30日的第二季度和上半年財務業績。公司第二季度淨利潤450萬美元,上半年淨利潤1450萬美元,分別實現了2520萬美元和5240萬美元的營業收入。這些數字相對於去年同期均出現營業收入下降的情況,歸因於在PRC因COVID19出現短暫增長後,他們的抗纖維化藥物ETUARY的銷售趨於正常化。Gyre Therapeutics公司突出了幾個業務更新,包括NMPA批准用於慢性肝病相關血小板減少症的avatrombopag maleate片劑,以及審批用於肺動脈高壓的F230的IND申請。公司還計...展開全部
2024年8月13日,商業化階段的生物技術公司Gyre Therapeutics公司公佈了截至2024年6月30日的第二季度和上半年財務業績。公司第二季度淨利潤450萬美元,上半年淨利潤1450萬美元,分別實現了2520萬美元和5240萬美元的營業收入。這些數字相對於去年同期均出現營業收入下降的情況,歸因於在PRC因COVID19出現短暫增長後,他們的抗纖維化藥物ETUARY的銷售趨於正常化。Gyre Therapeutics公司突出了幾個業務更新,包括NMPA批准用於慢性肝病相關血小板減少症的avatrombopag maleate片劑,以及審批用於肺動脈高壓的F230的IND申請。公司還計劃在2024年底前提交用於MASH相關肝纖維化的F351的美國IND,並預計在2025年初獲得CHb相關肝纖維化的第三階段試驗數據。截至2024年6月30日,Gyre Therapeutics的現金及現金等價物總計1610萬美元。報告還包括任命David m. Epstein爲董事會成員和該公司加入Russell 2000和Russell 3000指數。

譯文內容由第三人軟體翻譯。


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