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Clinical Trial Summary

The primary objective of this protocol is to evaluate [18F]MNI-1054 as a Lysine-specific histone demethylase 1A (LSD1) enzyme targeted radiopharmaceutical.


Clinical Trial Description

The primary objective of this protocol is to evaluate [18F]MNI-1054 as a Lysine-specific histone demethylase 1A (LSD1) enzyme targeted radiopharmaceutical. The specific objectives are:

- To measure the dynamic uptake and washout of [18F]MNI-1054 in brain using positron emission tomography (PET) in healthy volunteers.

- To measure blood metabolites of [18F]MNI-1054 in the healthy volunteers and to perform invasive as well as non-invasive modeling to assess its ability to measure LSD1 in the brain.

- To acquire safety data following injection of [18F]MNI-1054

- Evaluation of [18F]MNI-1054 PET reliability (test/retest) of the tracer parameters in healthy volunteers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03695926
Study type Interventional
Source Invicro
Contact
Status Completed
Phase Early Phase 1
Start date August 9, 2018
Completion date May 2, 2019