GEMINI-PeriOp GC study will assess the safety, tolerability, pharmacokinetics (PK) and preliminary anti-tumor activity of novel agents or novel combinations as perioperative treatment in participants with locally advanced resectable gastric, gastroesophageal junction (GEJ), or esophageal adenocarcinoma who have not received previous treatment for the disease.
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Number of participants with adverse events (AEs) and serious adverse events (SAEs)
Timeframe: Until sub-study completion, up to 38 months
Percentage of participants with pathological complete response (pCR)
Timeframe: Until sub-study completion, up to 38 months
AstraZeneca Clinical Study Information Center