Stopped: Business decision and not related to safety concerns
To characterize safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of QEQ278 in adult patients with advanced/metastatic non-small cell lung cancer, esophageal squamous cell carcinoma, renal cell carcinoma, and human papilloma virus associated head and neck squamous cell carcinoma.
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Incidence and nature of Dose Limiting Toxicities (DLTs) during the DLT evaluation period for single agent QEQ278
Timeframe: 28 days
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)
Timeframe: Up to 31 months
Frequency of dose interruptions, reductions
Timeframe: Up to 30 months
Dose intensity
Timeframe: Up to 30 months