CINJ # 052501 - A Phase 1/1b Study of IAM1363 in Participants with Advanced Cancers Harboring HER2 Alterations
Primary Objectives:
Part 1: To determine the MTD/MAD of IAM1363 as monotherapy.
Part 2: To determine the recommended dose of IAM1363 as monotherapy
Part 3: Part 3: To characterize the efficacy of IAM1363 as monotherapy
Secondary Objective:
Part 1: To further characterize the safety and efficacy of IAM1363 as monotherapy
Part 2: To further characterize the safety, tolerability, and efficacy of IAM1363 as monotherapy
Part 3: To further characterize the efficacy of IAM1363 as monotherapy
Part 3: To further evaluate the safety and tolerability of IAM1363 as monotherapy
Exploratory Objectives:
All Parts: To explore correlations between biomarkers and clinical outcomes
Parts 2 and 3: To evaluate the effect of IAM1363 on ECG parameters, including Concentration-QTc modeling
Part 1: To evaluate the impact of food on the PK of IAM1363
All Parts: To evaluate the concentration of IAM1363 in tumor and CSF samples
- Rutgers University
Key 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
Please note that we have obtained the inclusion and exclusion criteria information from the National Institutes of Health’s clinical trials web site ClinicalTrials.gov. The listed criteria may not necessarily reflect recent amendments to the protocol and the current criteria.
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