Sacituzumab Govitecan and Bevacizumab for NSCLC Brain Metastases
- Sponsor
- Maastricht University Medical Center
- Study ID
- NCT06401824
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Brain Metastases, Adult
- NSCLC Stage IV
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Sacituzumab Govitecan-Hziy 180 MG plus bevacizumab — DRUGSacituzumab govitecan 10mg/kg intravenous day 1 and day 8 of a 21-day cycle, + bevacizumab 15 mg/kg iv day 1 of a 21-day cycle till unacceptable toxicity or disease progression.
Study Details
This study will evaluate whether the combination of sacituzumab govitecan (SG) and bevacizumab will result in shrinkage of brain metastases from patients with non-squamous non-small cell lung cancer (NSCLC), with disease progression on chemotherapy and immunotherapy.
Key Dates
- First listed
- May 7, 2024
- Start date
- Apr 24, 2025
- Status verified
- May 2025
- Primary completion
- Nov 1, 2026
- Completion
- Apr 1, 2027
Study Design
- Enrollment
- 25 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: sacituzumab govitecan (SG) plus bevacizumabSG 10mg/kg intravenous day 1 and day 8 of a 21-day cycle, + bevacizumab 15 mg/kg iv day 1 of a 21-day cycle till unacceptable toxicity or disease progression.
Primary Outcome Measure
brain metastases overall response rate (ORR) [ Time Frame: up to 24 months ]
Central Contacts
- Lizza Hendriks, MD, PhD+31(0)43-3875047
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