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Puma Biotechnology to Present at the H.C. Wainwright Global Life Sciences Conference

Puma Biotechnology to Present at the H.C. Wainwright Global Life Sciences Conference

彪馬生物技術公司將在H.C.Wainwright全球生命科學大會上發言
Business Wire ·  2021/03/02 21:20

Puma Biotechnology, Inc. (NASDAQ: PBYI), a biopharmaceutical company, announced that Alan H. Auerbach, Chairman, Chief Executive Officer, President and Founder of Puma, will provide an overview of the Company at the H.C. Wainwright Global Life Sciences Conference, which will be held virtually on March 9-10, 2021. The presentation will be available on demand beginning at 7:00 a.m. EST on March 9, 2021.

彪馬生物技術公司。生物製藥公司(納斯達克股票代碼:PBYI)宣佈,彪馬董事長、首席執行官、總裁兼創始人艾倫·H·奧爾巴赫將在2021年3月9日至10日舉行的H.C.温賴特全球生命科學大會上介紹公司概況。演示文稿將於上午7:00開始按需提供。美國東部時間2021年3月9日。

The virtual presentation will be available for 30 days on the Company’s website at www.pumabiotechnology.com .

該虛擬演示文稿將在該公司的網站上發佈,為期30天,網址為:www.PumabioTechnology.com。

About Puma Biotechnology

關於彪馬生物技術

Puma Biotechnology, Inc. is a biopharmaceutical company with a focus on the development and commercialization of innovative products to enhance cancer care. Puma in-licenses the global development and commercialization rights to PB272 (neratinib, oral), PB272 (neratinib, intravenous) and PB357. Neratinib, oral was approved by the U.S. Food and Drug Administration in 2017 for the extended adjuvant treatment of adult patients with early stage HER2-overexpressed/amplified breast cancer, following adjuvant trastuzumab-based therapy, and is marketed in the United States as NERLYNX® (neratinib) tablets. In February 2020, NERLYNX was also approved by the FDA in combination with capecitabine for the treatment of adult patients with advanced or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2-based regimens in the metastatic setting. NERLYNX was granted marketing authorization by the European Commission in 2018 for the extended adjuvant treatment of adult patients with early stage hormone receptor-positive HER2-overexpressed/amplified breast cancer and who are less than one year from completion of prior adjuvant trastuzumab-based therapy. NERLYNX is a registered trademark of Puma Biotechnology, Inc.

彪馬生物技術公司是一家生物製藥公司,專注於創新產品的開發和商業化,以加強癌症護理。彪馬In-授權PB272(口服奈拉替尼)、PB272(奈拉替尼靜脈注射)和PB357的全球開發和商業化權利。奈拉替尼口服於2017年被美國食品和藥物管理局批准,用於繼以曲妥珠單抗為基礎的輔助性治療之後,用於早期her2過度表達/放大的成年乳腺癌患者的擴展輔助治療,並在美國以奈拉替尼(®)片劑的形式銷售。2020年2月,NERLYNX還被FDA批准與卡培他濱聯合用於治療晚期或轉移性HER2陽性乳腺癌的成年患者,這些患者之前在轉移環境中接受了兩種或更多基於HER2的抗化療方案。NERLYNX於2018年獲得歐盟委員會的營銷授權,可擴大對早期激素受體陽性HER2過度表達/擴增的成年乳腺癌患者的輔助治療,這些患者的年齡小於從之前的基於曲妥珠單抗的佐劑治療完成起一年。NERLYNX是彪馬生物技術公司的註冊商標。

Further information about Puma Biotechnology may be found at www.pumabiotechnology.com .

欲瞭解有關彪馬生物技術公司的更多信息,請訪問www.PumabioTechnology.com。

譯文內容由第三人軟體翻譯。


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