🔎 Trials Near Me

Home › Breast Cancer › NCT06253871

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

RecruitingPhase 1

A Phase 1/1b Study of IAM1363 in Participants With Advanced Cancers Harboring HER2 Alterations

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Key Inclusion Criteria:

* Age ≥ 18 years
* Have relapsed/refractory HER2-altered malignancy; for selected cohorts, prospective confirmation of HER2 alteration by central testing is required
* 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%
* Able to swallow oral medication

Key Exclusion Criteria:

* Clinically significant cardiac disease
* Infection with human immunodeficiency virus (HIV)-1 or HIV-2. Exception: Participants 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
* Prior history of non-infectious interstitial lung disease (ILD). (Exceptions: participants with prior grade 1 ILD that has completely resolved are eligible)
* Participants requiring immediate local therapy for brain metastases

About the study

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.

What is being tested

Sponsor: Iambic Therapeutics, Inc · Participants: 383 · Started: Mar 25, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06253871

Locations in the U.S.

CaliforniaUCSD Moores Cancer Center, La Jolla
USC Norris Comprehensive Cancer Center, Los Angeles
ColoradoUniversity of Colorado Cancer Center, Aurora
FloridaUniversity of Miami, Miami
Comprehensive Hematology Oncology, St. Petersburg
IllinoisUniversity of Chicago, Chicago
MassachusettsDana Farber Cancer Institute, Boston
Massachusetts General Hospital, Boston
MichiganUniversity of Michigan, Ann Arbor
Henry Ford Cancer Institute, Detroit
START - Midwest Cancer Research Center, Grand Rapids
MissouriSaint Luke's Cancer Institute, Kansas City
Washington University School of Medicine, St Louis
New HampshireDartmouth Hitchcock Medical, Lebanon
New JerseyRutgers Cancer Institute, New Brunswick
New YorkIcahn School of Medicine at Mount Sinai, New York
North CarolinaDuke Cancer Institute, Durham
OhioCleveland Clinic, Cleveland
University Hospital Cleveland Medical Center, Cleveland
OklahomaOU Health Stephenson Cancer Center, Oklahoma City
OregonProvidence Cancer Institute, Portland
TennesseeSCRI Oncology Partners, Nashville
Vanderbilt Ingram Cancer Center, Nashville
TexasNEXT Oncology - Austin, Austin
Mary Crowley Cancer Research, Dallas
MD Anderson Cancer Center - University of Texas, Houston
UtahSTART Mountain Region, West Valley City
VirginiaNEXT Oncology - Virginia Cancer Specialists, Fairfax
WashingtonFred Hutchinson Cancer Center, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.