This is a Phase 1/1b open-label, multi-center dose escalation and dose optimization study designed to evaluate the safety and preliminary efficacy of IAM1363 in participants with advanced cancers that harbor HER2 alterations.
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Incidence and severity of dose limiting toxicities (DLTs) (Part 1 only)
Timeframe: 21 days
Incidence and severity of adverse events (AEs)
Timeframe: Through 30 days after the last dose of study drug
Pharmacokinetic (PK) parameters
Timeframe: Up to 42 days
Confirmed objective response rate (cORR)
Timeframe: Through study completion, estimated as 46 months
Confirmed central nervous system ORR (CNS-cORR)
Timeframe: Through study completion, estimated as 46 months
Frequency of IAM1363 dose modifications, including treatment discontinuations
Timeframe: Through 30 days after the last dose of study drug
Incidence and severity of clinical laboratory abnormalities
Timeframe: Through 30 days post last dose of study drug
Incidence of ECG abnormalities
Timeframe: Through 30 days after the last dose of study drug
Iambic Therapeutics, Inc., Senior Medical Director