Stopped: Adjustment of drug development strategy.
This is a Phase 1b/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of D-1553 Combination Therapy in Subjects with KRAS G12C-mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer.
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Subject incidence of Dose-limiting toxicities (DLT)
Timeframe: Through out the DLT period, approximately 21 days
Number of subjects participants with adverse events
Timeframe: Till study completion, approximately 3 years
Antitumor activity of D-1553 in subjects with advanced or metastatic NSCLC with KRASG12C mutation
Timeframe: Till study completion, approximately 3 years