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Clinical Trial Summary

This is a first in man study to determine if [203Pb]VMT-α-NET identifies neuroendocrine tumors with SPECT/CT. This is the first step to testing [212Pb]-based alpha radiation therapy in neuroendocrine therapy.


Clinical Trial Description

The goal of this work is to use [203Pb]VMT-α-NET as the imaging agent to create a specialized patient treatment plan using [212Pb]VMT-α-NET as a first-in-human therapy for treatment resistant or refractory neuroendocrine tumors of the foregut or midgut. The first step is to test the imaging agent [203Pb]VMT-α-NET. This requires a very small dose of the drug (microdose) which is then measured by a series of images (like CT scans) over 4 days. Blood samples are also drawn that that time. It is hoped the imaging will identify the tumors so that a therapy using [212Pb]VMT-α-NET can be created. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05111509
Study type Interventional
Source University of Iowa
Contact
Status Enrolling by invitation
Phase Early Phase 1
Start date August 22, 2022
Completion date December 31, 2025

See also
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Active, not recruiting NCT06148636 - A Safety Study of 212Pb-VMT-alpha-NET in Patients With Neuroendocrine Tumors Early Phase 1
Not yet recruiting NCT06395402 - 177Lu-DOTATATE Modified Delivery Based on Individualized Dosimetry Phase 2