Study Title

lantheusmedicalimaging

A Phase 1/2a Study Utilizing 64Cu-LNTH-1363S (64Cu Radiolabeled FAPi PET/CT Imaging Agent) in Patients With Sarcoma or Gastrointestinal Tract Cancer (PHANTOM Trial)

Study Details

Description:

This is a multicenter, open-label, prospective Phase 1/2a study to assess safety and tolerability, establish dosimetry and to identify an optimal imaging dose (radioactivity and mass dose) and imaging time window of 64Cu-LNTH-1363S (64Cu Radiolabeled FAPi PET/CT Imaging Agent) and to compare its imaging biodistribution with FAP expression by immunohistochemistry (IHC) in patients with sarcomas or GIT cancers.

Contacts:

Eryn Bagley (Clinical Trial Lead)

eryn.bagley@lantheus.com

Drug Details

64Cu-LNTH-1363S
Isotope(s):
    COPPER-64
    Radioisotope: Cu-64
    Theranostic Role: PET Imaging
    T1/2 (Half-Life): 12.7 Hours
    Decay Mode: POSITRON β+, BETA, Electron Capture, GAMMA
    Energy: 0.65 MeV, Gamma 511 keV
    Range: max 2.5mm, mean 0.7mm
    Decay Daughters: Ni64 (Stable), Zn64 (Stable)
    Status: FDA Approval: DETECTNET®
  • COPPER-64
Target(s):
  • FAP

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