Evaluation of Patients With Refractory Dermatomyositis Using [18F] FAPI-74 PET/MRI Imaging

Part of paid clinical trials in Stanford, California.

Sponsor
Farshad Moradi
Study ID
NCT06568783
Phase
PHASE2
Status
Not Yet Recruiting

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Conditions

  • Refractory Dermatomyostitis

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • [18F]-FAPI-74 — DRUG
    \[18F\]-FAPI-74 7 mCi ± 20% administered intravenously.

Study Details

This study proposes the use of a PET isotope, \[18F\]-Fibroblast Activation Protein Inhibitor-74, for a prospective single-center, single-arm study using MRI imaging for participants with Refractory Dermatomyostitis.

Key Dates

Start date
Dec 31, 2024
Status verified
Nov 2024
Primary completion
Oct 31, 2027
Completion
Oct 31, 2028

Study Design

Enrollment
21 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: [18F]-FAPI-74 PET/ MRI
    Participant receive \[18F\]-FAPI-74 injection and approximately 45-60 minutes later receive a MRI scan from vertex to legs, followed by a static PET emission scan over the same area.

Primary Outcome Measure

Rate of [18F]-FAPI-74 uptake. [ Time Frame: up to 1 hour ]

Locations (1)

FacilityCityStateZIPSite coordinators
Stanford UniversityStanfordCalifornia94304-

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