Assertio Announces Results Of A Clinical Trial Investigating The Utility Of Rolvedon Injection When Dosed The Same Day Of Chemotherapy For Patients With Early Stage Breast Cancer
Assertio Announces Results Of A Clinical Trial Investigating The Utility Of Rolvedon Injection When Dosed The Same Day Of Chemotherapy For Patients With Early Stage Breast Cancer
Assertio Holdings, Inc. ("Assertio" or the "Company") (NASDAQ:ASRT), a pharmaceutical company with comprehensive commercial capabilities offering differentiated products to patients, announced yesterday results of a clinical trial investigating the utility of Rolvedon (eflapegrastim-xnst) injection when dosed the same day of chemotherapy for patients with early stage breast cancer (ESBC). The results were presented as part of the San Antonio Breast Cancer Symposium by the American Association of Cancer Research and the University of Texas Health Science Center at San Antonio.
Assertio Holdings, Inc.("Assertio"或"公司")(納斯達克:ASRT),是一家擁有綜合商業能力的藥品公司,向患者提供差異化產品,昨日宣佈了一項臨床試驗結果,研究Rolvedon(eflapegrastim-xnst)注射劑在接受化療當天對早期乳腺癌(ESBC)患者的療效。這些結果是在聖安東尼奧抗癌研討會由美國抗癌醫藥協會和德克薩斯大學健康科學中心在聖安東尼奧共同呈現的。
In this open-label, single-arm study (NCT04187898), conducted across 13 sites in the US, individuals received Rolvedon 30 minutes post chemotherapy for ESBC. Rolvedon demonstrated 1.8 days to neutrophil count recovery and a febrile neutropenia rate of 2%. Zero patients required the need for hospitalization and/or intervention for febrile neutropenia. No new safety signals were identified.
在這項開放標籤的單臂研究(NCT04187898)中,共在美國13個地點進行,受試者在化療後30分鐘接受Rolvedon治療。Rolvedon顯示出中性粒細胞計數恢復的時間爲1.8天,以及發熱性中性粒細胞減少症的發生率爲2%。沒有患者需要因發熱性中性粒細胞減少症住院和/或干預。未發現新的安全信號。
譯文內容由第三人軟體翻譯。