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Puma Biotechnology to Present at the H.C. Wainwright BioConnect Conference
Rhea-AI Impact
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Rhea-AI Sentiment
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Rhea-AI Summary
Puma Biotechnology (NASDAQ: PBYI) will present at the H.C. Wainwright BioConnect Virtual Conference, with CEO Alan H. Auerbach speaking on January 10, 2022, at 7:00 a.m. EST. The presentation will be available on the company’s website for 30 days. Puma focuses on developing innovative cancer therapies, including NERLYNX® (neratinib), approved for specific HER2-positive breast cancer treatments. NERLYNX is also indicated for advanced cases after prior therapies. Further details can be found on www.pumabiotechnology.com.
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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 provide an overview of the Company at the H.C. Wainwright BioConnect Virtual Conference. The presentation will be available on demand beginning at 7:00 a.m. EST on January 10, 2022.
The presentation will be available for replay for 30 days on the Company’s website at www.pumabiotechnology.com.
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. 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.
