Clinical trial

Imaging of Pathologic Fibrosis Using 68Ga-FAP-2286

Name
20-32872
Description
This is a single arm prospective pilot trial that evaluates the ability of a novel imaging agent (68Ga-FAP-2286) to identify pathologic fibrosis in the setting of hepatic, cardiac and pulmonary fibrosis. FAP-2286 is a peptide that potently and selectively binds to Fibroblast Activation Protein (FAP). FAP is a transmembrane protein expressed on fibroblasts and has been shown to have higher expression in idiopathic pulmonary fibrosis (IPF), cirrhosis, and cardiac fibrosis.
Trial arms
Trial start
2021-12-09
Estimated PCD
2024-12-31
Trial end
2024-12-31
Status
Recruiting
Phase
Early phase I
Treatment
68Ga-FAP-2286
A dose of 3 - 8 millicurie (mCi) will be given intravenously (IV)
Arms:
Cohort 1: Liver Fibrosis, Cohort 2: Pulmonary Fibrosis, Cohort 3: Myocardial Fibrosis
Other names:
68Gallium-Fibroblast Activation Protein-2286
Positron Emission Tomography (PET)
Imaging will begin 50-100 minutes after injection and last about 45 minutes.
Arms:
Cohort 1: Liver Fibrosis, Cohort 2: Pulmonary Fibrosis, Cohort 3: Myocardial Fibrosis
Other names:
PET Imaging, PET Scan
Size
30
Primary endpoint
Proportion of participants with treatment-related adverse events
Up to 31 days
Median peak standardized uptake value (SUVpeak) in liver region
Up to 1 days
Median peak standardized uptake value (SUVpeak) in lung region
Up to 1 days
Median peak standardized uptake value (SUV) in myocardium region
Up to 1 days
Eligibility criteria
Inclusion Criteria: 1. Age \>= 18 years. 2. Confirmed pathologic fibrosis in one of the following cohorts 1. Cohort 1: Hepatic fibrosis, based on cirrhosis on imaging or hepatic fibrosis on liver biopsy. 2. Cohort 2: Pulmonary fibrosis, based on CT findings or biopsy of lung parenchyma. 3. Cohort 3: High likelihood of cardiac fibrosis as indicated by known cardiac sarcoidosis or amyloidosis (shown on MRI or Fluorodeoxyglucose (FDG) PET), recent myocardial infarction within the last 30 days (as shown by an elevated troponin), known cardiotoxicity (decreased ejection fraction on systemic therapy), or other known inflammatory or infiltrative disease. 3. Ability to understand a written informed consent document, and the willingness to sign it. Exclusion Criteria: 1. Unlikely to comply with protocol procedures, restrictions and requirements and judged by the Investigator to be unsuitable for participation. 2. Known pregnancy.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'DIAGNOSTIC', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 30, 'type': 'ESTIMATED'}}
Updated at
2024-03-12

1 organization

1 product

3 indications

Organization
Thomas Hope