PET Imaging of Cannabinoid CB1 Receptors Using [18F]FMPEP-d2
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ClinicalTrials.gov Identifier: NCT00598286 |
Recruitment Status
:
Completed
First Posted
: January 21, 2008
Last Update Posted
: October 27, 2017
|
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
CB1 Cannabinoid PET Brain Imaging | Drug: [18F]FMPEP-d2 | Phase 1 |

BRAIN IMAGING
Objective
The central cannabinoid receptor (CB1) is one of the most abundant neuromodulatory receptors in the brain. It is found on glutamatergic, dopaminergic and GABA-ergic synaptic terminals and belongs to G-protein coupled receptor family. The CB1 is a target for drug therapy, including the use of an antagonist as an appetite suppressant. The central cannabinoid receptor CB1 has never been visualized in humans. In collaboration with Eli Lilly, we developed a promising PET ligand for the CB1 receptor: [18F]FMPEP-d2 ((3R,5R)-5-(3-(fluoromethoxy)phenyl)-3-((R)-1-phenylethylamino)-1-(4-(trifluoromethyl)phenyl)pyrrolidin-2-one).
Study Population
In the current protocol, we wish to evaluate [18F]FMPEP-d2 in approximately 10 healthy subjects.
Design
Brain imaging studies will consist of subject evaluation followed by PET and MRI scans.
Outcome Measures
We intend to determine the kinetics of brain uptake and washout, clearance in the plasma, and the distribution volume of [18F]FMPEP-d2 calculated with compartmental modeling. Distribution volume is proportional to the density of receptors and is equal to the ratio at equilibrium of uptake in brain to the concentration of parent radiotracer in plasma.
WHOLE BODY DOSIMETRY
Objective
Should the brain imaging studies prove to be successful, we will continue with whole body dosimetry studies. Preliminary dosimetry studies with [18F]d2-FMPEP have been performed in nonhuman primates; however, these need to be continued in humans before further investigation of this novel tracer can continue.
Study Population
In the current protocol, we wish to evaluate [18F]FMPEP-d2 in approximately 10 additional healthy subjects.
Design
The whole body dosimetry studies will consist of subject evaluation followed by a PET scan.
Outcome Measures
We intend to determine the whole body distribution of activity and thereby calculate radiation exposure to organs of the body.
BRAIN IMAGING WITH TEST/RE-TEST
Objective
Should the brain imaging and dosimetry studies prove to be successful, we will continue with test/retest brain imaging studies. Test/retest studies with [18F]FMPEP-d2 will provide evidence of reproducibility and strengthen the assurance that this radioligand can be used to assess pathology. Previous investigations in developing a CB1 receptor PET tracer have demonstrated the need to test reproducibility (Terry, In Writing; Burns et al 2007).
Study Population
In the current protocol, we wish to evaluate [18F]FMPEP-d2 in approximately 10 additional healthy subjects.
Design
The brain imaging test/retest studies will consist of subject evaluation followed by one MRI and two PET scans.
Outcome Measures
We intend to determine the reproducibility of the outcome measures from the brain imaging, namely, distribution volume.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 18 participants |
Allocation: | Non-Randomized |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Diagnostic |
Official Title: | Imaging of Cannabinoid CB1 Receptors Using [18F]FMPEP-d2 |
Study Start Date : | January 2008 |
Actual Primary Completion Date : | October 2009 |
Actual Study Completion Date : | October 2009 |

- Efficacy of novel PET tracer for CB1 in brain imaging.
- Distribution and variance of CB1 receptors in the brain of healthy controls.

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Ages Eligible for Study: | 18 Years to 65 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
- INCLUSION CRITERIA:
- All subjects must be healthy and aged 18-65 years, with history/physical exam, ECG, and laboratory tests within one year of the PET scan.
- The volunteer must sign an informed consent form.
EXCLUSION CRITERIA:
- Current psychiatric illness, substance abuse including marijuana use, or severe systemic disease based on history and physical exam.
- Laboratory tests with clinically significant abnormalities or positive urine toxicology screen.
- Prior participation in other research protocols in the last year such that radiation exposure would exceed the annual limits.
- Pregnancy and breast feeding.
- Claustrophobia.
- Presence of ferromagnetic metal in the body or heart pacemaker.
- Positive HIV test.
- Employee of the investigative site or an immediate family member of an employee of the investigative site. Immediate family member is defined as a spouse, parent, child, or sibling, whether biological or legally adopted.
- Employee of Eli Lilly and Company.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00598286
United States, Maryland | |
National Institutes of Health Clinical Center, 9000 Rockville Pike | |
Bethesda, Maryland, United States, 20892 |
Additional Information:
Publications:
Responsible Party: | Robert B. Innis, M.D./National Institute of Mental Health, National Institutes of Health |
ClinicalTrials.gov Identifier: | NCT00598286 History of Changes |
Other Study ID Numbers: |
080049 08-M-0049 |
First Posted: | January 21, 2008 Key Record Dates |
Last Update Posted: | October 27, 2017 |
Last Verified: | May 2012 |
Keywords provided by National Institutes of Health Clinical Center (CC):
CB1 Receptor PET Cannabinoid [18F]FMPEP-d2 |
Brain Imaging Healthy Volunteer HV |