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Compound · clinical trials

Meta-fluorobenzylguanidine clinical trials

Also listed in trial records as 18F-metaFluorobenzylguanidine, IRP101, 18F-mFBG for administration
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our USA register that name Meta-fluorobenzylguanidine as an intervention. Synced 29 Sep 2026
2Current trials
1Recruiting now
1Lead sponsor
1Country register
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Meta-fluorobenzylguanidine is named as an intervention in 2 current clinical trials in our USA register. 1 is recruiting patients now. The most common phase is Phase 2. The lead sponsor is Innervate Radiopharmaceuticals LLC (Formerly: Illumina Radiopharmaceuticals LLC). The most-studied condition is Heart Failure.

Trials by status

  • Recruiting150%
  • Active, closed150%

Trials by phase

  • Phase 2150%
  • Phase 1/2150%
01

Clinical trials of Meta-fluorobenzylguanidine

2 trials
StudyPhaseStatusLead sponsorRegisters
18F-mFBG Imaging for Myocardial Sympathetic Innervation
NCT06965621 · ClinicalTrials.gov ↗ · Heart Failure, Ischemic Cardiomyopathy, ICD Patients
Phase 2 Recruiting Innervate Radiopharmaceuticals LLC (Formerly: Illumina Radiopharmaceuticals LLC) USA
Open-Label Study of 18F-mFBG for Imaging Myocardial Sympathetic Innervation
NCT04535193 · ClinicalTrials.gov ↗ · Cardiovascular Diseases
Phase 1/2 Active, closed Innervate Radiopharmaceuticals LLC (Formerly: Illumina Radiopharmaceuticals LLC) USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Meta-fluorobenzylguanidine

4 conditions
Heart Failure1Ischemic Cardiomyopathy1ICD Patients1Cardiovascular Diseases1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Innervate Radiopharmaceuticals LLC (Formerly: Illumina Radiopharmaceuticals LLC)2
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA21

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Meta-fluorobenzylguanidine trials

How many clinical trials are testing Meta-fluorobenzylguanidine?

2 current trials in our USA register name Meta-fluorobenzylguanidine (also registered as 18F-metaFluorobenzylguanidine) as a drug or biological intervention, as of the registry sync on 29 September 2026. Completed and withdrawn studies are not counted.

Are Meta-fluorobenzylguanidine trials recruiting patients?

Yes. 1 of the 2 trials is recruiting: 1 with sites in USA. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Meta-fluorobenzylguanidine clinical trials?

The lead sponsor is Innervate Radiopharmaceuticals LLC (Formerly: Illumina Radiopharmaceuticals LLC). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Meta-fluorobenzylguanidine works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Meta-fluorobenzylguanidine works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Meta-fluorobenzylguanidine (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 29 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.