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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

Protocol Number: 052501
Phase: Phase I
Applicable Disease Sites: Any Site
Drugs Involved: IAM1363
Principal Investigator: Coral Omene
Scope: National
Therapies Involved: Chemotherapy single agent systemic
Participating Institutions:
  • Rutgers University
Inclusion & Exclusion Criteria

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.

For further information about clinical trials, please contact us at 732-235-7356.