ClinicalTrials.gg
Not yet recruitingNCT07933497Updated Nov 12, 2026

M4 Receptor PET Radioligand Validation Study in Healthy Adults

An Early Phase 1 interventional study of [11C]ABBV-112i in Healthy Volunteers, sponsored by AbbVie. Not yet recruiting. Open to participants aged 23 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-12.

Sponsored by AbbVie · Early Phase 1, Interventional, and Basic science

Updated Nov 12, 2026Newly registeredGo to Updates ↓
Phase
Early Phase 1
Study type
Interventional
Enrollment
6
Allocation
Not applicable
Ages
23 Years to 55 Years
Sex
All
01

Study summary

A radioligand is a small amount of a radioactive imaging compound used during a positron emission tomography (PET) scan. This study aims to validate a new positron emission tomography (PET) ligand for measuring M4 receptors in the brain. M4 receptors are proteins that may play a role in various psychiatric and neurological conditions. This study will evaluate the PET ligand [11C]ABBV-112i in healthy adult participants to assess how well the ligand can measure the distribution of the M4 receptors across brain regions and the test-retest variability of the binding measurements.

02

Conditions studied

  • Healthy Volunteers

Keywords

  • Healthy Volunteers
  • [11C]ABBV-112i
03

In context

Lead sponsor

AbbVie is the lead sponsor of 976 studies on the registry; 135 are open to participants now.

Of its 357 completed or terminated interventional studies of FDA-regulated products, 214 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
23 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • is >= 18.5 to \<= 29.9 kg/m2 after rounding to the tenths decimal at Screening. BMI is calculated as weight in kg divided by the square of height measured in meters.
  • A condition of general good health, based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead .

Exclusion criteria

Exclusion Criteria:

  • History of previous radiation exposure for research purposes such that participation in this study will result in cumulative ionizing radiation exposure >10 mSv in the past 12 months, in addition to normal background exposure
  • Unable or unwilling to undergo CT, PET, or arterial cannulation procedures.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

05

Study design

Phase
Early Phase 1
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
6 participants (estimated)

Study arms

  • Experimental
    [11C]ABBV-112i

    Participants will receive two single intravenous bolus doses of \[11C\]ABBV-112i, with each dose followed by up to approximately 90 minutes dynamic PET scan.

    Drug: [11C]ABBV-112i

Interventions

  • Drug[11C]ABBV-112i

    Intravenous Bolus

06

What researchers measure

Primary outcomes

  1. Regional brain volume of distribution (VT) of ABBV-112i across brain regions

    VT defined as the ratio of radioligand concentration in the tissue region of interest to that observed in plasma at equilibrium.

    Time frame: Up to Approximately Up to Day 1

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Feb 2027, 3 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 6, 2026
First posted
Nov 12, 2026
StartEst.
Nov 10, 2026
Primary completionEst.
Feb 2027
CompletionEst.
Feb 2027
Last update
Nov 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 12, 2026
Show all 1 update
  1. Nov 12, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07933497
Lead sponsor
AbbVie
Responsible party
Sponsor
First posted
Nov 12, 2026
Start date
Nov 10, 2026 (estimated)
Primary completion
Feb 2027 (estimated)
Completion
Feb 2027 (estimated)
Last update
Nov 12, 2026

Study contacts

ABBVIE CALL CENTER
Contact
abbvieclinicaltrials@abbvie.com
844-663-3742
ABBVIE INC.
study director · AbbVie

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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