OTHERClinicalTrials.govClinical trialRecruiting
Preliminary Assessment of [18F]BL40 in PET/CT Scans
Official record
- Identifier
NCT06224309- Recruiting locations
country
Canada- Interventions studied
- 18F-BL40 PET/CT18F-FDG PET/CTRoutine Blood Draw - Phase 1 only
- Lead sponsor
- British Columbia Cancer Agency
- Target enrolment
- 30 participants
- Study type
- OBSERVATIONAL
- Phase
- Not provided in the official record
- Status
- Recruiting
- First posted
- Jan 25, 2024
- Last updated on the registry
- Oct 1, 2026
- Age
- 19 Years – 100 Years
- Sex
- ALL
- Study contact
- The official record lists a study contact. Contact details are published there and are intentionally not copied to this page.
- Eligibility criteria
Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.
Inclusion Criteria: 1. Age ≥19 years 2. Life expectancy ≥3 months 3. Eastern Cooperative Oncology Group (ECOG) performance status 0-2 4. Participants with newly diagnosed or documented recurrent malignancy with one of the following cancers: * Diffuse large B-Cell lymphoma * Multiple myeloma * Mantle cell lymphoma * Marginal zone lymphoma * Chronic lymphocytic leukemia/small cell lymphoma * Waldenström Macroglobulinemia Exclusion Criteria: 1. Pregnant or breast-feeding 2. Medically unstable (e.g., acute illness, unstable vital signs) 3. Unable to lie supine for the duration of imaging 4. Unable to provide written consent 5. Exceeds safe weight limit of the PET/CT bed (204.5 kg) or unable to fit through the PET/CT bore (diameter 70 cm) 6. Participants with a history of uncontrolled allergic reactions and/or known or expected hypersensitivity to the peptide diagnostic \[18F\]BL40 or any of its excipients.
- Indexed under
- Leukemia