A Study of Oral MBQ-167 in Participants With Advanced Breast Cancer
Part of paid clinical trials in Beverly Hills, California.
- Sponsor
- MBQ Pharma
- Study ID
- NCT06075810
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Breast Cancer
- Breast Cancer Stage IV
- Breast Neoplasm
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- MBQ-167 — DRUGMBQ-167, an inhibitor of Rho GTPases Rac and Cdc42
Study Details
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.
Key Dates
- Start date
- Nov 9, 2023
- Status verified
- Dec 2024
- Primary completion
- Oct 1, 2025
- Completion
- Oct 31, 2025
Study Design
- Enrollment
- 48 participants (estimated)
- Allocation
- NA
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: MBQ-167 oral capsuleA dose ranging from 10mg to 400mg BID following a standard 3+3 cohort design
Primary Outcome Measure
Maximum Tolerated Dose (MTD) [ Time Frame: 21 days ]
Central Contacts
- Scott Houston(415) 404 8838
- Jose Rodriguez-Orengo, PhD
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Precision Next Gen Oncology & Research Center | Beverly Hills | California | 90212 | Kumar Sankhala, MD (PRINCIPAL_INVESTIGATOR) |
| Florida Cancer Specialists / Sarah Cannon Research Institute / SCRI | Sarasota | Florida | 34232 | Judy S Wang, MD (PRINCIPAL_INVESTIGATOR) |
| Sarah Cannon Research Institute/SCRI | Nashville | Tennessee | 37203 | Denise Yardley, MD (PRINCIPAL_INVESTIGATOR) |
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