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.
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.
A Phase 1/1b Study of IAM1363 in HER2 Cancers
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USC Norris Comprehensive Cancer Center, Los Angeles, California, United States, 90089
Comprehensive Hematology Oncology, Saint Petersburg, Florida, United States, 33709
University of Michigan, Ann Arbor, Michigan, United States, 48109
START - Midwest Cancer Research Center, Grand Rapids, Michigan, United States, 49546
Cleveland Clinic, Cleveland, Ohio, United States, 44195
OU Health Stephenson Cancer Center, Oklahoma City, Oklahoma, United States, 73104
SCRI Oncology Partners, Nashville, Tennessee, United States, 37203
NEXT Oncology - Austin, Austin, Texas, United States, 78758
NEXT Oncology - Dallas, Dallas, Texas, United States, 75039
Mary Crowley Cancer Research, Dallas, Texas, United States, 75230
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
For general information about clinical research, read Learn About Studies.
18 Years to
ALL
No
Iambic Therapeutics, Inc,
Iambic Therapeutics, Inc., Senior Medical Director, STUDY_DIRECTOR, Iambic Therapeutics, Inc
2028-03