12 Participants NeededMy employer runs this trial

Granzyme-B Radiotracers for Healthy Volunteers

NP
EC
AC
Overseen ByAnna Carberry
Age: 18 - 65
Sex: Any
Trial Phase: Phase < 1
Sponsor: Ratio Therapeutics, Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This is an exploratory clinical study of copper-64 \[Cu-64\]-labeled granzyme B (GzmB)-targeted compounds for PET/CT imaging. The goal is to determine how GzmB-Targeted \[Cu-64\]-labeled compounds are distributed in the body by assessing PET/CT images and blood samples, and to assess the safety profile after a single intravenous dose.

Up to 6 healthy volunteers (3 female, 3 male) will receive one injection of a GzmB-targeted \[Cu-64\]-labeled compound, then undergo multiple whole-body PET/CT scans, blood and urine tests over about 24 hours, and a follow-up phone call around Day 7. Up to 2 GzmB-Targeted \[Cu-64\]-labeled compounds may be assessed (i.e. maximum of 12 healthy volunteers in total in the study).

Researchers will look at the blood activity of GzmB-Targeted \[Cu-64\]-labeled compound and the organ distribution and movement of the product in the body. They will also evaluate any changes in physical examination assessments, vital signs, ECG, and clinical laboratory measurements from pre-administration to post-administration.

Are You a Good Fit for This Trial?

This trial is for healthy adults who are willing to receive a single injection of an experimental imaging compound and undergo several scans and tests over about 24 hours. Participants must not have any health conditions that could interfere with the study.

Inclusion Criteria

I am between 18 and 60 years old and in good health.
My liver and kidney function tests are normal.
I am able to understand and sign the consent form for this study.
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Exclusion Criteria

Known allergy/hypersensitivity to PET/CT tracers or compounds similar to GzmB-Targeted Compounds
Concurrent participation in a clinical trial of investigational product(s)
I have or may have an inflammatory, autoimmune, or fibrotic disease.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants receive a single intravenous dose of a GzmB-targeted [Cu-64]-labeled compound followed by serial whole-body PET/CT imaging, blood and urine sampling for pharmacokinetics and excretion, and safety assessments over approximately 24 hours post-dose.

24 hours
Multiple visits within 24 hours (in-person)

Follow-up

Participants receive a follow-up phone call to monitor safety and effectiveness approximately 7 days after the treatment.

7 days
1 visit (phone call)

What Are the Treatments Tested in This Trial?

Interventions

  • Granzyme-B targeted [64Cu]-labeled PET radiotracer

Trial Overview

Researchers are testing how a new PET/CT imaging agent, which targets granzyme B and contains copper-64, moves through and is processed by the body after one injection. Up to two similar compounds may be studied in small groups of healthy volunteers.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: [Cu-64]RTX-4002Experimental Treatment1 Intervention
Group II: [Cu-64]RTX-4001Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Ratio Therapeutics, Inc.

Lead Sponsor

Trials
1
Recruited
20+