18F-mFBG Cardiac Uptake With Lewy Body Dementia

Last updated: March 25, 2026
Sponsor: Innervate Radiopharmaceuticals LLC (Formerly: Illumina Radiopharmaceuticals LLC)
Overall Status: Active - Recruiting

Phase

2

Condition

Parkinson's Disease

Lewy Body Dementia

Treatment

18F-MFBG

Clinical Study ID

NCT07176286
IRP101-231
  • Ages > 18
  • All Genders

Study Summary

This is a Phase 2 study evaluating the positron-emitting radiopharmaceutical 18F-mFBG as an imaging agent for quantification of the effect of neurodegenerative diseases on myocardial sympathetic innervation. Effectiveness of 18F-mFBG imaging of the heart will be judged in terms of the quantitative difference between results for subjects with Lewy body and non-Lewy body neurologic disease as compared to historical data for healthy control subjects.

Eligibility Criteria

Inclusion

Inclusion Criteria:

    1. ≥18 years of age at study entry. 2. Able and willing to comply with studyprocedures and signed and dated informed consent is obtained.

  1. A male or a female who is either surgically sterile (has had a documentedbilateral oophorectomy and/or hysterectomy), postmenopausal (cessation of menses formore than 1 year), non-lactating, or of childbearing potential for whom the resultof a serum pregnancy test performed at screening is negative.

  2. All subjects: Judged clinically stable for at least 30 days before enrolment intothe study and remains stable to the time of the study imaging procedure.

For Lewy body disease subjects (Study Cohort I):

  1. The subject has a diagnosis of either PD or DLB based on accepted clinical criteria at least 6 months before enrollment into the study.

For non-Lewy body disease subjects (Study Cohort II):

  1. The subject has a diagnosis of neurological or neurodegenerative disease for which neither PD nor DLB is judged likely by a neurologist based on accepted clinical and imaging criteria.

Exclusion

Exclusion Criteria:

    1. Previously entered into this study or has participated in any otherinvestigational product or medical device study within 30 days of enrollment.

  1. History or suspicion of significant allergic reaction or anaphylaxis to anycomponents of the 18F-mFBG imaging agent.

  2. Presents with any other clinically active, serious, life-threatening disease witha life expectancy of less than 1 year or where participation in the study mightcompromise the management of the subject or other reason that in the judgment of theinvestigator(s) makes the subject unsuitable for participation in the study.

  3. Documented ischemic heart disease (prior myocardial infarction, unstable angina,etc) or a diagnosis of heart failure of ischemic or non-ischemic etiology.

  4. Serious non-cardiac medical condition associated with significant elevation ofplasma catecholamines including pheochromocytoma.

  5. The subject is claustrophobic or has a movement disorder that prevents him/herfrom lying still in a supine position for up to 20 minutes.

  6. Renal insufficiency (serum creatinine >3.0 mg/dL). 8. Uses medications that areknown to interfere with uptake of NET-dependent agents and these medications cannotbe safely withheld 24 hours before study procedures.

  7. Participated in a research study using ionizing radiation in the previous 12months such that participation in the study might result in a total effective dosefrom research procedures exceeding 50 milliSieverts during that time interval.

Study Design

Total Participants: 20
Treatment Group(s): 1
Primary Treatment: 18F-MFBG
Phase: 2
Study Start date:
April 15, 2026
Estimated Completion Date:
October 30, 2026

Study Description

Over the past 40 years, significant efforts have been made to develop imaging techniques to monitor the heart's autonomic nervous system, particularly the sympathetic system and its key neurohormone, norepinephrine (NE). In heart disease, NE function is often disrupted, leading to reduced NE uptake and transporter expression, which can contribute to heart failure, arrhythmias, and sudden cardiac death. Similar NE system dysfunction is also seen in neurological conditions like pure autonomic failure (PAF), Parkinson's disease (PD), and Dementia with Lewy Bodies (DLB), which are associated with Lewy body deposits in the nervous system. Most research on myocardial sympathetic neuronal imaging has focused on NE-analogues labeled with gamma- or positron-emitting radioisotopes. The most commonly studied agent is 123I-mIBG, which provides semi-quantitative data. However, its results depend heavily on imaging equipment and techniques, making global standardization difficult. Additionally, accurately measuring myocardial uptake and clearance is challenging with SPECT, even when using correction methods. While most cardiac mIBG research has focused on patients with heart disease, a significant number of studies have examined the effect of Lewy body disease on myocardial sympathetic innervation. These studies have consistently demonstrated a significant reduction in myocardial mIBG uptake. mIBG scintigraphy has high sensitivity (88%) and specificity (85%) for distinguishing Parkinson's disease (PD) from other Parkinsonism disorders. In a study of 123I-mIBG scans, the heart/mediastinum ratio (HMR) showed 68.9% sensitivity and 89.1% specificity for differentiating dementia with Lewy bodies (DLB) from Alzheimer's disease (AD). Neurologists and movement disorder specialists find mIBG imaging helpful for assessing suspected Lewy body disease. Positron-emission tomography (PET) is the preferred method for high-resolution imaging of cellular functions. This study uses 18F-meta-fluorobenzylguanidine (18F-mFBG), a new radiopharmaceutical similar in structure to 123I-mIBG but with faster pharmacokinetics and elimination. Compared to 123I-mIBG, 18F-mFBG clears more quickly from the blood and target organs, resulting in better heart imaging quality and reliability. While most research on 18F-mFBG has focused on imaging neural crest tumors like neuroblastoma and pheochromocytoma, its performance is expected to be strong based on prior experience with 123I-mIBG. With the greater sensitivity and resolution of PET imaging compared to planar and SPECT techniques, it is expected that 18F-mFBG imaging will be less procedure-dependent than 123I-mIBG and provide the reliable and reproducible quantitative accuracy necessary to support use of this agent for clinical patient studies.

Connect with a study center

  • Houston Methodist Neurological Institute

    Houston, Texas 77030
    United States

    Active - Recruiting

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.