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Clinical Trials Search at Vanderbilt-Ingram Cancer Center

A Phase 1/1b Study of IAM1363 in HER2 Cancers

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.
Miscellaneous
Phase I
Adults
Mol. targeted/Immunotherapy/Biologics
IAM1363
Kennedy, Laura
National
Vanderbilt University
11-05-2025
Treatment
VICCPHI24527
NCT06253871

Eligibility

18 Years and older
ALL
false
Inclusion Criteria:

Age 18 years

Have relapsed/refractory HER2-altered malignancy

Have progression of disease after the last systemic therapy, or be intolerant of last systemic therapy

Have radiographically measurable disease by RECIST v1.1 and/or RANO-BM

Eastern Cooperative Oncology Group (ECOG) performance score 0-1

Have adequate baseline hematologic, liver and renal function

Have left ventricular ejection fraction (LVEF) 50%



Exclusion Criteria:

Clinically significant cardiac disease

Infection with human immunodeficiency virus (HIV)-1 or HIV-2. Exception: Patients with well-controlled HIV (e.g., CD4 >350/mm3 and undetectable viral load) are eligible

Current active liver disease including hepatitis A, hepatitis B , or hepatitis C

Refractory nausea and vomiting, malabsorption, external biliary shunt, or significant small bowel resection that would preclude adequate absorption

Uncontrolled diabetes

History of solid organ transplantation

History of Grade 2 CNS hemorrhage, or any CNS hemorrhage within 28 days before C1D1

Patients requiring immediate local therapy for brain metastases

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trials, call 615-936-8422.