This study will evaluate the recommended dose for further clinical development, safety, tolerability, anti-tumor activity, immunogenicity, pharmacokinetics and pharmacodynamics of IKS014, a HER2 targeting antibody-drug conjugate, in patients with advanced solid tumors.
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Recommended Phase 2 Dose (Part 1)
Timeframe: Up to 24 months
Objective Response Rate (Part 2)
Timeframe: Up to 24 months