ZIIHERA Plus TEVIMBRA and Chemotherapy: A Potential New Standard for First-Line HER2+ Advanced GEA
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced full results from the Phase 3 HERIZON-GEA-01 trial evaluating ZIIHERA® (zanidatamab), a HER2-targeted bispecific antibody, in combination with chemotherapy, with and without PD-1 inhibitor TEVIMBRA® (tislelizumab), as a first-line treatment for HER2-positive (HER2+) locally advanced or metastatic gastroesophageal adenocarcinoma (GEA). These data, includin
Sonrotoclax Data at ASH 2025 Confirm Foundational Potential Across B-cell Malignancies
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced new data on sonrotoclax, a next-generation investigational BCL2 inhibitor, demonstrating meaningful clinical benefit as monotherapy and in combination across B-cell malignancies. These data were featured at the 67th American Society of Hematology (ASH) Annual Meeting & Exposition in Orlando, Florida. The five presentations highlight durable responses
BeOne Medicines Announces Positive Topline Results for Sonrotoclax in Relapsed or Refractory Mantle Cell Lymphoma (MCL)
ONC(NASDAQ:ONC) SAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced positive topline results from a Phase 1/2 study (BGB-11417-201) of sonrotoclax, a next-generation and potentially best-in-class investigational BCL2 inhibitor, in adult patients with relapsed/refractory (R/R) mantle cell lymphoma (MCL), following treatment with a Bruton’s tyrosine kinase inhibitor (BTKi) and anti-CD20 therapy. BeOne plans to present the f
European Commission Approves TEVIMBRA® as Neoadjuvant/Adjuvant NSCLC Treatment Ahead of Late-Breaking Data Presentation at WCLC 2025
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that the European Commission (EC) has approved TEVIMBRA (tislelizumab), in combination with platinum-containing chemotherapy as neoadjuvant treatment followed by TEVIMBRA monotherapy as adjuvant treatment, for adult patients with resectable non-small cell lung cancer (NSCLC) at high risk of recurrence. The EC approval is based on results from the Phase 3
BeOne to Present at the Morgan Stanley 23rd Annual Global Healthcare Conference
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced it will participate in the Morgan Stanley 23rd Annual Global Healthcare Conference on September 8, 2025, with a fireside chat at 1:50 p.m. EDT. The live webcast of this event can be accessed from the investors section of the Company’s website at https://ir.beonemedicines.com, https://hkexir.beonemedicines.com, https://sseir.beonemedicines.com. An archived
BeOne Medicines Announces IMDELLTRA Royalty Purchase Agreement for up to $950 Million
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced it has entered into an agreement to sell its royalty rights on the worldwide sales, excluding China, of Amgen’s IMDELLTRA® (tarlatamab-dlle) for up to $950 million to Royalty Pharma (Nasdaq: RPRX). Under the terms of the agreement, BeOne will receive an upfront payment of $885 million, with the option to sell remaining royalties within 12 months for up to
Biotech Stocks Rally as Oncology Market Targets $866B by 2034
ONCEquity Insider News Commentary Issued on behalf of Oncolytics Biotech Inc. VANCOUVER, BC, Aug. 14, 2025 /PRNewswire/ -- Equity Insider News Commentary – Despite alarming federal budget cuts that stand to potentially harm the national battle against cancer, it appears that the private...
BeOne Medicines Announces Second Quarter 2025 Financial Results and Business Updates
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced financial results and corporate updates from the second quarter of 2025. “Our strong second quarter performance reinforces our trajectory as a global oncology powerhouse and underscores our proven ability to deliver sustainable, long-term growth,” said John V. Oyler, Co-Founder, Chairman and CEO of BeOne. “We are executing with purpose and advancing our m
BeOne Medicines Showcases Breakthrough Data in CLL and MCL at EHA 2025
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company, will present new clinical data from three cornerstone hematology assets at the European Hematology Association (EHA) Congress. Four oral presentations highlight the promising clinical activity of BeOne’s next-generation BCL2 inhibitor sonrotoclax, BTK protein degrader BGB-16673, and the backbone of our hematology franchise, BTK inhibitor BRUKINSA (zanubrutinib), which ha
BeOne Medicines Showcases Breakthrough Data in CLL and MCL at EHA 2025
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company, will present new clinical data from three cornerstone hematology assets at the European Hematology Association (EHA) Congress. Four oral presentations highlight the promising clinical activity of BeOne’s next-generation BCL2 inhibitor sonrotoclax, BTK protein degrader BGB-16673, and the backbone of our hematology franchise, BTK inhibitor BRUKINSA (zanubrutinib), which ha
BeOne Medicines Receives FDA Approval For A New Tablet Formulation Of BRUKINSA For All Five Approved Indications
ONCU.S. FDA Approves Tablet Formulation of BeOne’s BRUKINSA® for All Approved Indications
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that the U.S. Food and Drug Administration (FDA) has approved a new tablet formulation of BRUKINSA® (zanubrutinib) for all five approved indications. BRUKINSA remains the leader in new chronic lymphocytic leukemia (CLL) patient starts across all lines of therapy in the U.S., and for the first time, has become the overall BTK inhibitor market share leader.
BeOne Medicines to Host Investor R&D Day Webcast on June 26, 2025
ONCSAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that it will host an Investor R&D Day in New York City and via webcast on June 26, 2025 at 8:30 am ET. John V. Oyler, Co-Founder, Chairman, and CEO of BeOne, along with the Company's leadership team and distinguished key opinion leaders, will provide an update on BeOne’s extensive global innovation pipeline and platforms, including new assets, targets
BeOne Medicines Announced New Clinical Data From Its Breast Cancer Pipeline At The American Society Of Clinical Oncology Annual Meeting, Poster Presentations Feature Preliminary Results Of The Dose Escalation Studies Of: BG-C9074 For Advanced Solid Tumors
ONCReported Saturday, BeOne's SEQUOIA Trial Shows BRUKINSA Plus Venetoclax Yields Deep, Durable Responses Across CLL Risk Groups Including del(17p) And TP53
ONCThe Committee For Medicinal Products For Human Use Of The European Medicines Agency Issued A Positive Opinion Recommending Approval Of BeiGene's Tevimbra (Tislelizumab), In Combination With Gemcitabine And Cisplatin, For Adult Patients With Recurrent, Not
ONCBeiGene to Present 23 Cancer Drug Studies at ASCO, Including Data on BRUKINSA and Breast Cancer Treatments
ONCEarnings Preview: BeiGene
ONCRBC Capital Maintains Outperform on BeiGene, Lowers Price Target to $311
ONCGuggenheim Maintains Buy on BeiGene, Raises Price Target to $350
ONCCORRECTION: BeiGene Affirms FY2025 Sales Guidance of $4.90B-$5.30B Vs. $5.09B Estimate
ONCCORRECTION: BeiGene Q1 Adj. EPADS $1.22 Beats $(0.74) Estimate, Sales $1.12B Miss $1.14B Estimate
ONCBeiGene Affirms FY2025 Sales Guidance of $4.90B-$5.30B vs $36.54B Est
ONCBeiGene Q1 Adj. EPS $1.22 Beats $(0.74) Estimate, Sales $1.12B Miss $8.09B Estimate
ONCUSPTO Renders Final Decision, Invalidating All Challenged Pharmacyclics Patent Claims Against BeiGene
ONCRBC Capital Reiterates Outperform on BeiGene, Maintains $312 Price Target
ONCTD Securities Reiterates Buy on BeiGene, Maintains $334 Price Target
ONCJP Morgan Maintains Overweight on BeiGene, Raises Price Target to $317
ONCGuggenheim Reiterates Buy on BeiGeneto Buy
ONCForecasting The Future: 4 Analyst Projections For BeiGene
ONCGuggenheim Reiterates Buy on BeiGene, Maintains $348 Price Target
ONCRBC Capital Initiates Coverage On BeiGene with Outperform Rating, Announces Price Target of $312
ONCBeiGene Has Discontinued Its Clinical Development Program For Ociperlimab (BGB-a1217), An Anti-TIGIT Antibody, As A Potential Treatment For Lung Cancer
ONCBeiGene Secures Positive CHMP Opinion For TEVIMBRA As First-Line Treatment For Extensive-Stage Small Cell Lung Cancer
ONCChina-Based Biotech BeiGene Scores FDA Approval For Tevimbra/Chemo Combo For Untreated Patients With Esophageal Cancer
ONCBeiGene's Tevimbra wins FDA approval for first-line metastatic ESCC treatment, showing significant survival benefits in PD-L1-positive patients.
FDA Approves TEVIMBRA In US For The First-Line Treatment Of Adults with Unresectable Or Metastatic Esophageal Squamous Cell Carcinoma (ESCC)
ONCMacquarie Maintains Outperform on BeOne Medicines, Raises Price Target to $313
ONCCitizens Capital Markets Maintains Market Outperform on BeOne Medicines, Raises Price Target to $348
ONCBeiGene Expects 2025 Total Revenue Of $4.9B-$5.3B Versus $3.81B YoY
ONCBeiGene Q4 2024 GAAP EPADS $(1.43) Up From $(3.53) YoY, Sales $1.13B Versus $634.41M YoY
ONC