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Amgen and AstraZeneca Combo Cuts Death Risk 58% in Small Cell Lung Cancer as ESMO 2026 Produces Wave of Oncology Data
Read this in the Market Flux appAmgen and AstraZeneca reported landmark Phase 3 results at the European Society for Medical Oncology Congress 2026 in Madrid showing that Imdelltra, Amgen's tarlatamab-dlle, combined with AstraZeneca's Imfinzi, durvalumab, reduced the risk of death by 58% compared with Imfinzi alone as a first-line maintenance treatment in patients with extensive-stage small cell lung cancer, one of the fastest-growing and most lethal cancers. The hazard ratio came in at 0.42, and shares of Amgen were up roughly 0.5% in premarket trading on the news.
Xencor emerged as another standout from the Madrid meeting, with shares surging more than 33% before the open after the company selected 400 mcg/kg as the proposed intravenous recommended Phase 3 dose for XmAb819, its ENPP3 x CD3 T-cell engaging bispecific antibody targeting advanced clear cell renal cell carcinoma. Phase 1 expansion-cohort data underpinning that choice showed a 45.5% confirmed objective response rate, a 55% unconfirmed ORR, and an estimated 82% six-month progression-free survival rate. Xencor said it plans to seek FDA discussions on accelerated approval in the first half of 2027 and intends to design a tivozanib-controlled pivotal trial.
Several other companies posted clinical updates across oncology indications at ESMO 2026. Corcept Therapeutics reported positive results from the Phase 2 BELLA trial of Lifyorli combined with nab-paclitaxel and bevacizumab in platinum-resistant ovarian cancer. BioNTech and Bristol Myers Squibb released first Phase 2 data for pumitamig, a PD-L1xVEGF-A bispecific immunomodulator, in combination with docetaxel for metastatic non-small cell lung cancer from the ROSETTA Lung-107 trial. Nuvectis Pharma reported durable responses including complete responses for NXP200 in BRAF V600-mutated recurrent or progressive gliomas in a Phase 1b study. Insilico Medicine disclosed a 40% objective response rate at the 130 mg dose for its AI-designed pan-TEAD inhibitor ISM6331 in heavily pretreated mesothelioma. Amarin shares rose 4.3% premarket after icosapent ethyl showed a survival benefit in a cancer trial, and Nanobiotix was up 5.6% premarket following final Phase 1 data for NBTXR3 with immune checkpoint inhibitors in anti-PD-1-resistant primary cutaneous melanoma.
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- BioStocks$CORT Reports Positive Results from Phase 2 BELLA Trial of Lifyorli Combined with Nab-Paclitaxel and Bevacizumab in Patients with Platinum-Resistant Ovarian Cancer
- Briefingcom$XNCR: Xencor selected 400 mcg/kg as XmAb819’s proposed Phase 3 dose after Phase 1 data showed a 45.5% confirmed response.
- NasdaqBioNTech SE and Bristol Myers Squibb Report Phase 2 Data for Pumitamig in Advanced NSCLC
- OpenOutcrier$AMGN (+0.5% pre) Amgen says drug combo cuts risk of death by 58% in patients with aggressive lung cancer
- BPharmCatalyst$XNCR selected 400 mcg/kg as the Phase 3 XmAb819 dose after Phase 1 ccRCC data showed a 45.5% confirmed ORR, 55% unconfirmed ORR, and 82% estimated 6-month PFS. Xencor plans 1H 2027 FDA talks on accelerated approval and a tivozanib-controlled trial. While early-stage, it offers a key late-stage opportunity. $SPRC $BOLT $ERNA $AARD $XNCR $CPIX $EOCN $MCRB $IBO $LABT See More Pre-market Movers at BioPharmCatalyst in the Articles Menu
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