Competitive intelligence
CI feed
Conference abstracts + payer decisions interleaved chronologically — the CI team aims to publish a structured briefing within 48 hours of any high-relevance event landing here.
12 items in window · 0 high-relevance
- Congressmediumembargo lifts in 1dJun 1, 2026, 9:15 PMTecentriq plus chemotherapy in previously untreated NSCLC: updated analysis from IMpower-16Median OS 19.6 months. HR 0.75 (95% CI 0.64–0.86). Grade ≥3 AEs consistent with prior reports.Tecentriq () · RocheNSCLCIMpower-16 · NCT45181053Trials in Progress Poster SessionOS19.6 monthsHR 0.75 (0.64-0.86)PFS10.1 monthsHR 0.74 (0.64-0.88)ORR51.2 percent
- Congressmediumembargo lifts in 1dJun 1, 2026, 10:00 PMKeytruda plus chemotherapy in previously untreated TNBC: updated analysis from KEYNOTE-560Median OS 18 months. HR 0.83 (95% CI 0.71–0.95). No new safety signals identified.Keytruda () · MerckTNBCKEYNOTE-560 · NCT60389648Poster Discussion SessionOS18 monthsHR 0.83 (0.71-0.95)PFS11 monthsHR 0.81 (0.74-0.94)ORR41.2 percent
- Congressmediumembargo lifts in 2dJun 2, 2026, 3:30 PMCheckMate-957: Opdivo (nivolumab) neoadjuvant in HCCMedian OS 19.2 months. HR 0.62 (95% CI 0.51–0.73). No new safety signals identified.Opdivo () · Bristol-Myers SquibbHCCCheckMate-957 · NCT64844073Education SessionOS19.2 monthsHR 0.62 (0.51-0.73)PFS8.6 monthsHR 0.64 (0.54-0.74)ORR32.5 percent
- Congressmediumembargo lifts in 2dJun 2, 2026, 4:45 PMReal-world effectiveness of Opdivo vs standard of care in RCCMedian OS 51.4 months. HR 0.83 (95% CI 0.74–0.92). No new safety signals identified.Opdivo () · Bristol-Myers SquibbRCCCheckMate-903 · NCT76925924Oral Abstract SessionOS51.4 monthsHR 0.83 (0.74-0.92)PFS23.3 monthsHR 0.83 (0.75-0.92)ORR55.7 percent
- Congressmediumembargo lifts in 2dJun 2, 2026, 9:30 PMReal-world effectiveness of Keytruda vs standard of care in TNBCMedian OS 24 months. HR 0.81 (95% CI 0.69–0.93). No new safety signals identified.Keytruda () · MerckTNBCKEYNOTE-968 · NCT24586311Poster SessionOS24 monthsHR 0.81 (0.69-0.93)PFS7.2 monthsHR 0.79 (0.7-0.97)ORR40.4 percent
- Congressmediumembargo lifts in 3dJun 3, 2026, 3:00 PMDESTINY-Breast-179: Enhertu (trastuzumab deruxtecan) adjuvant in gastricMedian OS 18.8 months. HR 0.88 (95% CI 0.74–0.99). No new safety signals identified.Enhertu () · Daiichi SankyogastricDESTINY-Breast-179 · NCT43607208Publication OnlyOS18.8 monthsHR 0.88 (0.74-0.99)PFS7.9 monthsHR 0.89 (0.72-0.97)ORR49.7 percent
- Congressmediumembargo lifts in 3dJun 3, 2026, 4:45 PMLong-term follow-up of Opdivo neoadjuvant for NSCLC: CheckMate-845Median OS 29.2 months. HR 0.58 (95% CI 0.48–0.68). Grade ≥3 AEs consistent with prior reports.Opdivo () · Bristol-Myers SquibbNSCLCCheckMate-845 · NCT53991773Late-Breaking Oral Abstract SessionOS29.2 monthsHR 0.58 (0.48-0.68)PFS10.6 monthsHR 0.55 (0.44-0.65)ORR47.7 percent
- Congressmediumembargo lifts in 4dJun 4, 2026, 8:15 PMReal-world effectiveness of Lynparza vs standard of care in HR+ breast cancerMedian OS 38 months. HR 0.62 (95% CI 0.48–0.76). No new safety signals identified.Lynparza () · AstraZenecaHR+ breast cancerOlympiA-594 · NCT43314812Poster Discussion SessionOS38 monthsHR 0.62 (0.48-0.76)PFS23.1 monthsHR 0.61 (0.47-0.76)ORR63.1 percent
- Congressmediumembargo lifts in 4dJun 4, 2026, 9:00 PMLong-term follow-up of Tecentriq 3L+ for NSCLC: IMpower-860Median OS 20.7 months. HR 0.88 (95% CI 0.76–0.99). No new safety signals identified.Tecentriq () · RocheNSCLCIMpower-860 · NCT14419528Education SessionOS20.7 monthsHR 0.88 (0.76-0.99)PFS11.4 monthsHR 0.85 (0.76-0.96)ORR40.1 percent
- Congressmediumembargo lifts in 4dJun 4, 2026, 9:30 PMLong-term follow-up of Verzenio 1L for HR+ breast cancer: MONARCH-252Median OS 33.1 months. HR 0.68 (95% CI 0.6–0.76). No new safety signals identified.Verzenio () · Eli LillyHR+ breast cancerMONARCH-252 · NCT49268597Poster SessionOS33.1 monthsHR 0.68 (0.6-0.76)PFS21.5 monthsHR 0.65 (0.6-0.78)ORR74.8 percent
- Congressmediumembargo lifts in 5dJun 5, 2026, 3:15 PMBiomarker subgroup analysis of Imfinzi in NSCLC (the PACIFIC-569 study)Median OS 16.4 months. HR 0.85 (95% CI 0.75–0.95). No new safety signals identified.Imfinzi () · AstraZenecaNSCLCPACIFIC-569 · NCT82451698Education SessionOS16.4 monthsHR 0.85 (0.75-0.95)PFS9.1 monthsHR 0.87 (0.78-0.99)ORR50.7 percent
- Congressmediumembargo lifts in 5dJun 5, 2026, 7:15 PMLong-term follow-up of Trodelvy 3L+ for urothelial carcinoma: ASCENT-421Median OS 12.5 months. HR 0.8 (95% CI 0.72–0.88). Grade ≥3 AEs consistent with prior reports.Trodelvy () · Gileadurothelial carcinomaASCENT-421 · NCT53826507Poster SessionOS12.5 monthsHR 0.8 (0.72-0.88)PFS8.7 monthsHR 0.8 (0.69-0.84)ORR31.6 percent