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Overview
The objective of this clinical trial is to determine the safety of an intravenously administered radiotracer, RAD301 ([68Ga]-Trivehexin), in either healthy volunteers or patients with pancreatic cancer. All participants will undergo: Screening, which entails physical examination and blood samples for standard blood testing. Participants that successfully pass screening will undergo: Gallium-68 PET scanning procedures, which will occur during a single day (about 5-6 hours). These participants will return to the clinic at 2 weeks for additional safety labs. All scanned participants will also be evaluated by telephone follow up on a weekly basis for 1 month after scanning.
Sponsor
Radiopharm TheranosticsPhase
Phase 1
Contacts
Lionel S Zuckier, MD
lzuckier@montefiore.org
(+1) 718 405 8454
ClinicalTrials.gov
NCT05799274Drug / Compound
Eligibility
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