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Clinical Trial Summary

A Phase 1, open-label, dose-escalation clinical trial of MBQ-167 in participants with advanced Breast Cancer for whom Standard of Care (SOC) has failed or has proven intolerable.


Clinical Trial Description

The main questions this clinical trial aims to answer are: - What, if any, are the side effects of different dose levels in humans? - What is the maximum tolerated dose? - How does the human body process the drug? - Does the drug slow, stop or eliminate cancer in human participants? Participants will be asked to: - provide informed consent - be evaluated by physicians and provide laboratory specimens to determine if eligible - take MBQ-167 orally twice a day for at least 21 days - may continue dosing, if safe to do so, until not effective or other decision to stop is made - participate in multiple visits that include additional evaluations, laboratory tests and diary review until after stopping the investigational drug ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06075810
Study type Interventional
Source MBQ Pharma
Contact Scott Houston
Phone (415) 404 8838
Email scott.houston@mbqpharma.com
Status Recruiting
Phase Phase 1
Start date November 9, 2023
Completion date October 31, 2024

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