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Allarity Therapeutics | 8-K: Current report

Allarity Therapeutics | 8-K: Current report

Allarity Therapeutics | 8-K:重大事件
美股SEC公告 ·  2024/09/17 20:04

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Allarity Therapeutics announced that two patients in its Phase 2 clinical trial of stenoparib for advanced, recurrent ovarian cancer have surpassed one year of treatment. These patients were pre-screened using Allarity's Drug Response Predictor (DRP®) companion diagnostic, which identified them as likely responders to the dual PARP/Tankyrase inhibitor treatment.The trial, conducted at multiple sites in the US and UK, implements a revised protocol with twice-daily dosing of stenoparib (200mg morning, 400mg evening). The enrolled patients, who had previously undergone multiple treatments including platinum, taxanes, and PARP inhibitors, demonstrated sustained clinical benefit with confirmed complete response and long-term disease stability.CEO Thomas Jensen emphasized the significance of extending life by 52 weeks in heavily pre-treated patients. The company is actively planning to accelerate stenoparib's path toward regulatory approval, with additional program updates expected in the coming months.
Allarity Therapeutics announced that two patients in its Phase 2 clinical trial of stenoparib for advanced, recurrent ovarian cancer have surpassed one year of treatment. These patients were pre-screened using Allarity's Drug Response Predictor (DRP®) companion diagnostic, which identified them as likely responders to the dual PARP/Tankyrase inhibitor treatment.The trial, conducted at multiple sites in the US and UK, implements a revised protocol with twice-daily dosing of stenoparib (200mg morning, 400mg evening). The enrolled patients, who had previously undergone multiple treatments including platinum, taxanes, and PARP inhibitors, demonstrated sustained clinical benefit with confirmed complete response and long-term disease stability.CEO Thomas Jensen emphasized the significance of extending life by 52 weeks in heavily pre-treated patients. The company is actively planning to accelerate stenoparib's path toward regulatory approval, with additional program updates expected in the coming months.
Allarity Therapeutics宣佈,其針對晚期複發性卵巢癌的stenoparib二期臨牀試驗中有兩名患者的治療超過了一年。這些患者通過Allarity的藥物反應預測器(DRP®)伴隨診斷進行預先篩選,識別爲對雙PARP/Tankyrase抑制劑治療可能有反應者。該試驗在美國和英國的多個地點進行,實施了修訂的方案,每日兩次服用stenoparib(早晨200mg,晚上400mg)。註冊的患者之前已接受多種治療,包括鉑金、紫杉烯和PARP抑制劑,顯示出持續的臨牀益處,確認完全響應和長期疾病穩定。首席執行官托馬斯·延森強調,在重度預處理患者中延長生命52周的重要性。公司正積極計劃加速stenoparib的監管批准路徑,並預計在未來幾個月內提供更多項目更新。
Allarity Therapeutics宣佈,其針對晚期複發性卵巢癌的stenoparib二期臨牀試驗中有兩名患者的治療超過了一年。這些患者通過Allarity的藥物反應預測器(DRP®)伴隨診斷進行預先篩選,識別爲對雙PARP/Tankyrase抑制劑治療可能有反應者。該試驗在美國和英國的多個地點進行,實施了修訂的方案,每日兩次服用stenoparib(早晨200mg,晚上400mg)。註冊的患者之前已接受多種治療,包括鉑金、紫杉烯和PARP抑制劑,顯示出持續的臨牀益處,確認完全響應和長期疾病穩定。首席執行官托馬斯·延森強調,在重度預處理患者中延長生命52周的重要性。公司正積極計劃加速stenoparib的監管批准路徑,並預計在未來幾個月內提供更多項目更新。
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