PET and MRI Imaging of Brain Tumors Using [18F]PARPi
Early Phase 1
Active, not recruiting
- Conditions
- Brain CancerBrain Tumor
- Interventions
- Diagnostic Test: PET/MR with [18F]PARPiDrug: [18F]PARPi
- Registration Number
- NCT04173104
- Lead Sponsor
- Memorial Sloan Kettering Cancer Center
- Brief Summary
This study is to collect data about how 18FPARPi can be used together with PET/positron emission tomography and MRI/magnetic resonance imaging scans to take pictures of brain cancer
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
- Patients with new or suspected recurrent brain tumors (including suspected recurrent brain tumors showing growth from any preceding scan)
- Age >/= 18 years
- Minimum at least one brain lesion size >/= 1.5cm diameter
- Scheduled to undergo treatment at MSK
- Willingness to sign informed consent
- Able to receive intravenous gadolinium contrast per MSK Department of Radiology guidelines
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Exclusion Criteria
- Any contraindication to 3T MRI (PET/MR scanner is 4.0 Tesla)
- Pregnancy or breast-feeding women
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Participants with Brain Cancer PET/MR with [18F]PARPi Participants with new or suspected recurrent brain tumors Participants with Brain Cancer [18F]PARPi Participants with new or suspected recurrent brain tumors
- Primary Outcome Measures
Name Time Method SUVmax measurements Up to 24 weeks \[18F\]PARPi updtake in lesions will be quantified by standard SUVmax measurements from PET/MR scans
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Memorial Sloan Kettering Cancer Center
🇺🇸New York, New York, United States