A First-in-human Clinical Trial to Evaluate an Alpha-radiation Imaging Agent

EARLY_PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

August 22, 2022

Primary Completion Date

April 30, 2026

Study Completion Date

June 30, 2026

Conditions
Neuroendocrine Tumor Grade 2Neuroendocrine Tumor Grade 1
Interventions
DRUG

[203Pb]VMT-α-NET

3 to 5 miliCuries of \[203\]Pb administered intravenously 60 minutes before the start of the scans.

DEVICE

SPECT/CT

Scans are administered over 3 days: 1 hour post injection, 4 to 8 hours post-injection, 24 to 30 hours post-injection, and 42 to 52 hours post-injection.

Trial Locations (1)

52242

The University of Iowa, Iowa City

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Perspective Therapeutics

INDUSTRY

collaborator

Holden Comprehensive Cancer Center

OTHER

collaborator

National Cancer Institute (NCI)

NIH

lead

Yusuf Menda

OTHER