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.
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% Key
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
Additional locations may be listed on ClinicalTrials.gov for NCT06253871.
Locations matching your search criteria
United States
California
La Jolla
Los Angeles
Colorado
Aurora
Florida
Miami
Massachusetts
Boston
Michigan
Ann Arbor
Missouri
Saint Louis
New Jersey
New Brunswick
Ohio
Cleveland
Oklahoma
Oklahoma City
Texas
Houston
Washington
Seattle
This is a Phase 1/1b open-label, multi-center study, designed to evaluate IAM1363 in
participants with advanced cancers that harbor HER2 alterations.
This study consists of the following 3 parts, which are described in further detail
below:
- Part 1 (Monotherapy Dose Escalation)
- Part 2 (Dose Optimization)
- Part 3 (Simon 2-Stage Evaluation)
Part 1 will enroll participants with a confirmed, relapsed/refractory malignancy with
documented diagnosis of HER2 alterations including participants with brain metastases.
Once a provisional maximum tolerated dose (MTD)/recommended Phase 2 dose (RP2D) has been
determined, Part 2 will enroll additional cohorts to optimize dose selection and to
further evaluate the safety and preliminary efficacy of IAM1363. Following completion of
Dose Optimization, Part 3 will be opened to enroll tumor-specific cohorts utilizing a
Simon 2-Stage Minimax Design to evaluate IAM1363 at the selected dose(s).
Trial PhasePhase I
Trial Typetreatment
Lead OrganizationIambic Therapeutics, Inc
- Primary IDIAM1363-01
- Secondary IDsNCI-2024-02383
- ClinicalTrials.gov IDNCT06253871