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Clinical Translation of a Novel FAPI Dimer [68Ga]Ga-LNC1013

C

Central South University

Status

Completed

Conditions

Gastrointestinal Cancer

Treatments

Diagnostic Test: 68Ga-FAPI dimer(68Ga-LNC1013)

Study type

Observational

Funder types

Other

Identifiers

NCT06159049
PETcenter

Details and patient eligibility

About

Fibroblast activation protein (FAP) emerges as a highly promising target for cancer diagnostic imaging and targeted radionuclide therapy. To exploit the therapeutic potential of current FAP inhibitors (FAPIs), this study presented the design and synthesis of a series of FAPI dimers to increase tumor uptake and retention. Preclinical evaluation and a pilot clinical PET imaging study were conducted to screen the lead compound with the potential for radionuclide therapy.

Full description

Three new FAPI dimers were synthesized by linking two quinoline-based FAPIs with different spacers. The in vitro binding affinity and preclinical small animal PET imaging of the compounds were compared with their monomeric counterparts, FAPI-04 and FAPI-46. The lead compound, 68Ga-LNC1013, was then evaluated in a pilot clinical PET imaging study involving seven patients with gastrointestinal cancer.

Enrollment

7 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Histologically and/or clinically confirmed and/or suspicious of gastrointestinal cancer.
  2. Signed informed consent.

Exclusion criteria

  1. pregnancy;
  2. breastfeeding;
  3. any medical condition that in the opinion of the investigator may significantly interfere with study compliance.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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