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Puma Biotechnology to Participate in Breast Cancer Panel at Cowen’s Annual Health Care Conference
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Rhea-AI Summary
Puma Biotechnology, Inc. (NASDAQ: PBYI) announced that Alan H. Auerbach, its CEO, will participate in a breast cancer panel at Cowen's 42nd Annual Health Care Conference. This virtual event is scheduled for Wednesday, March 9, at 2:10 p.m. ET. A live webcast will be available on Puma's website and archived for 30 days. Puma focuses on developing innovative cancer treatments, with products like NERLYNX® (neratinib) aimed at HER2-positive breast cancer.
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LOS ANGELES--(BUSINESS WIRE)--
Puma Biotechnology, Inc. (Nasdaq: PBYI), a biopharmaceutical company, announced that Alan H. Auerbach, Chairman, Chief Executive Officer, President and Founder of Puma, will participate in a panel discussion on breast cancer at Cowen’s 42nd Annual Health Care Conference, which will be held virtually. The Breast Cancer Panel will take place on Wednesday, March 9, at 2:10 p.m. ET.
A live webcast of the presentation will be available on the Company’s website at https://www.pumabiotechnology.com. The presentation will be archived on the website and available for 30 days.
About Puma Biotechnology
Puma Biotechnology, Inc. is a biopharmaceutical company with a focus on the development and commercialization of innovative products to enhance cancer care. The Company 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 (FDA) 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-positive 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.