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Gyre Therapeutics | 10-Q: Quarterly report

Gyre Therapeutics | 10-Q: Quarterly report

Gyre Therapeutics | 10-Q:季度報表
美股SEC公告 ·  08/14 04:07
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Gyre Therapeutics, a commercial-stage biotechnology company, reported a net income of $4.5 million for the three months ended June 30, 2024, and $14.5 million for the six months ended June 30, 2024. This represents an increase from the previous year's figures of $3.8 million and $8.0 million, respectively, for the same periods. The company's accumulated deficit as of June 30, 2024, was $74.5 million, with cash and cash equivalents totaling $16.1 million. Gyre Therapeutics focuses on developing and commercializing anti-inflammatory and anti-fibrotic drugs, with a particular emphasis on organ fibrosis. The company has successfully commercialized ETUARY (Pirfenidone) in multiple regions and is expanding its product portfolio through acquisitions and clinical trials. In May 2024, Gyre acquired rights to nintedanib, a drug for idiopathic pulmonary fibrosis, and received approval...Show More
Gyre Therapeutics, a commercial-stage biotechnology company, reported a net income of $4.5 million for the three months ended June 30, 2024, and $14.5 million for the six months ended June 30, 2024. This represents an increase from the previous year's figures of $3.8 million and $8.0 million, respectively, for the same periods. The company's accumulated deficit as of June 30, 2024, was $74.5 million, with cash and cash equivalents totaling $16.1 million. Gyre Therapeutics focuses on developing and commercializing anti-inflammatory and anti-fibrotic drugs, with a particular emphasis on organ fibrosis. The company has successfully commercialized ETUARY (Pirfenidone) in multiple regions and is expanding its product portfolio through acquisitions and clinical trials. In May 2024, Gyre acquired rights to nintedanib, a drug for idiopathic pulmonary fibrosis, and received approval for avatrombopag maleate tablets for thrombocytopenia associated with chronic liver disease. The company is also advancing its lead candidate, F351, for liver fibrosis treatment, with a Phase 3 trial ongoing in the PRC and plans for a Phase 2a trial in the United States. Gyre Therapeutics has regained compliance with Nasdaq's audit committee composition requirements after recent board appointments. Looking ahead, the company intends to use cash flows from operations to meet financial obligations and fund operations, including clinical trials and potential commercial launches.
生物技術公司Gyre Therapeutics報告2024年6月30日結束的3個月內淨利潤爲450萬美元,6個月內淨利潤爲1450萬美元。這比去年同期的380萬美元和800萬美元分別提高。截至2024年6月30日,該公司累計赤字爲7450萬美元,現金及現金等價物爲1610萬美元。Gyre Therapeutics專注於開發和商業化抗炎和抗成纖維藥物,特別關注器官纖維化。該公司已在多個地區成功商業化ETUARY(Pirfenidone),通過收購和臨床試驗擴大其產品組合。2024年5月,Gyre獲得了治療特發性肺纖維化藥物nintedanib的權利,並獲得了治療慢性肝病血小板減少症的avatro...展開全部
生物技術公司Gyre Therapeutics報告2024年6月30日結束的3個月內淨利潤爲450萬美元,6個月內淨利潤爲1450萬美元。這比去年同期的380萬美元和800萬美元分別提高。截至2024年6月30日,該公司累計赤字爲7450萬美元,現金及現金等價物爲1610萬美元。Gyre Therapeutics專注於開發和商業化抗炎和抗成纖維藥物,特別關注器官纖維化。該公司已在多個地區成功商業化ETUARY(Pirfenidone),通過收購和臨床試驗擴大其產品組合。2024年5月,Gyre獲得了治療特發性肺纖維化藥物nintedanib的權利,並獲得了治療慢性肝病血小板減少症的avatrombopag男酸鹽片的批准。該公司還在推進其首席候選藥F351,用於治療肝纖維化,在中國進行了3期試驗,並計劃在美國進行2a期試驗。Gyre Therapeutics最近的董事會任命後已恢復了納斯達克審計委員會組成要求的合規性。展望未來,該公司打算使用運營現金流來滿足財務義務和資助運營,包括臨床試驗和潛在的商業發佈。

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