Amgen reports 58 percent lower death risk in trial for Amgen stock
π Amgen reported a 58 percent lower risk of death in the DeLLphi-305 Phase 3 trial for an Imdelltra and Imfinzi combination in extensive-stage small cell lung cancer.
β±οΈ Median overall survival reached 21.10 months with the combination versus 12.70 months with Imfinzi alone, while progression-free survival improved to 7.40 months from 1.90 months.
π₯ Nearly 80 percent of patients in the combination group were alive after one year compared to 53 percent for those receiving Imfinzi alone.
β οΈ The combination therapy resulted in a higher incidence of Grade 3 or higher treatment-related adverse events at 20.90 percent versus 10.80 percent for Imfinzi monotherapy.
π° Amgen's second-quarter oncology portfolio generated approximately USD 2 billion, with Imdelltra sales rising 115 percent year over year to USD 288 million.
π The company raised its full-year 2026 revenue outlook to a range of USD 38.2 billion to USD 39.4 billion following the strong second-quarter performance.
π’ Amgen reported second-quarter adjusted earnings per share of USD 6.29 on total revenue of USD 10.05 billion.
π The stock traded at EUR 395.63 with a market capitalization of USD 237.5 billion as of October 23, 2026.
- Amgen demonstrated a 58 percent lower risk of death in the DeLLphi-305 Phase 3 trial for its Imdelltra and Imfinzi combination therapy.
- Median overall survival in the trial reached 21.10 months with the combination versus 12.70 months with Imfinzi alone, indicating a significant efficacy boost.
- Nearly 80 percent of patients in the combination group survived past one year compared to 53 percent for the monotherapy group.
- Amgen raised its full-year 2026 revenue outlook to USD 38.2 billion-USD 39.4 billion following a strong second quarter.
- The company achieved second-quarter revenue of USD 10.05 billion and adjusted earnings per share of USD 6.29.
- The Imdelltra and Imfinzi combination therapy was associated with a higher rate of Grade 3 or higher treatment-related adverse events at 20.90 percent compared to 10.80 percent for Imfinzi alone.
- Regulatory review and commercial execution remain critical next steps required before the new indication can materially reshape the company's growth.