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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

彪马生物技术公司将在H.C.Wainwright全球生命科学大会上发言
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.

彪马生物技术公司。生物制药公司(纳斯达克股票代码:PBYI)宣布,彪马董事长、首席执行官、总裁兼创始人艾伦·H·奥尔巴赫将在2021年3月9日至10日举行的H.C.温赖特全球生命科学大会上介绍公司概况。演示文稿将于上午7:00开始按需提供。美国东部时间2021年3月9日。

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

该虚拟演示文稿将在该公司的网站上发布,为期30天,网址为:www.PumabioTechnology.com。

About Puma Biotechnology

关于彪马生物技术

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.

彪马生物技术公司是一家生物制药公司,专注于创新产品的开发和商业化,以加强癌症护理。彪马In-授权PB272(口服奈拉替尼)、PB272(奈拉替尼静脉注射)和PB357的全球开发和商业化权利。奈拉替尼口服于2017年被美国食品和药物管理局批准,用于继以曲妥珠单抗为基础的辅助性治疗之后,用于早期her2过度表达/放大的成年乳腺癌患者的扩展辅助治疗,并在美国以奈拉替尼(®)片剂的形式销售。2020年2月,NERLYNX还被FDA批准与卡培他滨联合用于治疗晚期或转移性HER2阳性乳腺癌的成年患者,这些患者之前在转移环境中接受了两种或更多基于HER2的抗化疗方案。NERLYNX于2018年获得欧盟委员会的营销授权,可扩大对早期激素受体阳性HER2过度表达/扩增的成年乳腺癌患者的辅助治疗,这些患者的年龄小于从之前的基于曲妥珠单抗的佐剂治疗完成起一年。NERLYNX是彪马生物技术公司的注册商标。

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

欲了解有关彪马生物技术公司的更多信息,请访问www.PumabioTechnology.com。

译文内容由第三方软件翻译。


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