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.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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
Iambic Therapeutics, Inc., Senior Medical Director
Incidence of ECG abnormalities
Timeframe: Through 30 days after the last dose of study drug