Table of Contents
- Trial overview
- Who participated
- What was measured
- Study design and phase
- Condition focus: Crohn’s disease
Trial overview
This article covers one clinical trial of VERCIRNON, identified as 2022-502843-36-00, which was a completed Phase 1 interventional study.[1] The study used a PET scan approach to examine where the radiotracer [11C]AZ14132516 goes in the body after VERCIRNON was given.[1]
Who participated
The trial enrolled 9 healthy participants.[1] Even though the participants were healthy, the study was linked to Crohn’s disease research because the condition was listed in the trial data.[1]
What was measured
The main results were standard uptake value (SUV) and standard uptake value ratio (SUVR) in regions of interest.[1] These scan measures help show how much tracer is taken up and how much total binding occurs to CCR9 in the body areas being studied.[1]
The brief summary says the study aimed to examine the distribution of [11C]AZ14132516 and its binding to CCR9 in anatomical regions of interest in the abdominal area.[1] In simple words, researchers wanted to see where the tracer traveled and how it behaved in the belly area on the scan.[1]
Study design and phase
This was an interventional study, which means researchers gave the study intervention and then observed the results.[1] It was in Phase 1, the earliest stage of clinical research, which is often used to gather first information about how a study test performs in people.[1]
Condition focus: Crohn’s disease
The only condition named in the source data was Crohn’s disease.[1] The trial did not describe treatment of symptoms; instead, it focused on imaging and binding measurements that may help researchers study this condition in the abdominal area.[1]



