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Puma Biotechnology(PBYI-Q)
NASDAQ

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Day Low6.07
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Open:6.14
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Top Stories: Puma Biotechnology

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Puma Biotechnology Balances Growth, Trials and Profitability
Analysts Are Neutral on Top Healthcare Stocks: Puma Biotechnology (PBYI), Cytek Biosciences (CTKB)
Puma Biotechnology’s Earnings Call: Balancing Growth and Challenges
Puma Biotechnology (PBYI) Receives a Sell from Barclays
Puma Biotechnology Reports Q3 2025 Financial Results
Puma Biotechnology Reports Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
Puma Biotechnology Reports Third Quarter 2025 Financial Results
Puma Biotechnology’s Phase 2 Study of Alisertib: A Promising Update for Investors
Puma Biotechnology to Host Conference Call to Discuss Third Quarter Financial Results
Puma Biotechnology Reports Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
Puma Biotechnology Reports Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
Puma Biotechnology to Present at the H.C. Wainwright 27th Annual Global Investment Conference
Puma Biotechnology Reports Strong Q2 2025 Earnings
Puma Biotechnology Reports Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
Puma Biotechnology Reports Second Quarter Financial Results
Puma Biotechnology to Host Conference Call to Discuss Second Quarter 2025 Financial Results
Puma Biotechnology Reports Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
The Future of Medicine: Key Biotech Stocks to Watch
Puma Biotechnology Reports Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
Puma Biotechnology Reports First Quarter Financial Results
Puma Biotechnology to Host Conference Call to Discuss First Quarter 2023 Financial Results

Profile

Puma Biotechnology, Inc. is a small cancer biotech whose only marketed product, Nerlynx (neratinib) was launched in the United Statesfor the treatment of early stage HER2-positive breast cancer in patients who have been previously treated with Roche's Herceptin-based adjuvant therapy. The drug was also approved in the European Union. Nerlynx in combination with Roche's Xeloda was approved'by the Food and Drug Administration for third-line HER2-positive metastatic breast cancer. Meanwhile, several additional studies on Nerlynx targeting different types of breast cancer patient populations as well as other types of cancers are currently underway. A key analysis of Nerlynx is the phase II SUMMIT basket study for treating solid tumors in patients with activating EGFR, HER2 or HER4 mutated cancers. Puma markets Nerlynx in the United States and has several sub-licenses in various regions outside the United States to commercialize Nerlynx in some international markets.