A Phase 1a/1b Study of the PI3Ka: RAS Breaker BBO-10203 in Subjects with Advanced Solid Tumors (The BREAKER-101 Trial)
Dose Escalation and Dose Expansion Study of BBO-10203 in Subjects with Advanced Solid Tumors
Sponsor: TheRas Inc., d.b.a. BridgeBio Oncology Therapeutics
Enrolling: Male and Female Patients
IRB Number: AAAV5636
U.S. Govt. ID: NCT06625775
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: The purpose of this study is to find the best dose and effects of BBO-10203 when used alone or in combination with Trastuzumab in HER2-positive advanced breast cancer (aBC) or HR-positive, HER2-negative aBC or advanced non-small cell lung cancer (aNSCLC) with a KRAS (Kirsten rat sarcoma) mutation or advanced colorectal cancer (aCRC) with a KRAS mutation. BBO-10203 has not been approved by the Food and Drug Administration (FDA). Trastuzumab is FDA approved but not in combination with BBO-10203. This is a first in human study.
Do You Qualify?
Are you 18 years old or older? Yes No
Do you have a life expectancy of more than 12 weeks? Yes No
Are you able to swallow tablets intact without chewing or crushing? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162