GSK reports encouraging early Ris-Rez data in small-cell lung cancer

On 18 October 2026, GSK reported global phase Ib results for investigational risvutatug rezetecan in relapsed extensive-stage small-cell lung cancer. The drug produced a 61% objective response rate at 8 mg/kg among evaluable patients, versus 32% at 6 mg/kg. GSK said the findings support use of the higher dose in the ongoing global phase III EMBOLD SCLC-301 study, with further data due at ESMO Congress 2026.

The 8 mg/kg regimen is now being taken forward in a global phase III study, moving Ris-Rez toward a potentially registrational test in relapsed extensive-stage small-cell lung cancer. The reported safety data will remain relevant as development advances, particularly because higher-dose treatment had more grade 3 or higher treatment-related adverse events.

  • 1The phase Ib dose-optimisation analysis included 50 patients who had received a median of two prior therapies.
  • 2Grade 3 or higher treatment-related adverse events affected 42% of patients at 8 mg/kg and 15% at 6 mg/kg.
  • 3Interstitial lung disease occurred in 2% of the overall study population, or 1 out of 50 patients, and the case was grade 2.
  • 4The trial data are scheduled for presentation in a poster session at the ESMO Congress 2026 in Madrid, Spain.

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