Tracers / [177Lu]Lu-FAP-2286

[177Lu]Lu-FAP-2286

Also written as [Lu-177]Lu-FAP-2286; FAP-2286; Lu-177-FAP-2286
Radionuclide
Lu-177 t½ 9584.6 min
Modality
Therapy
Production route
Stage
first-in-human
Syntheses indexed
4

What it is

Compound class
FAP-binding cyclic peptide conjugate (FAP-2286)
Target / mechanism
Targets fibroblast activation protein (FAP) PMID 34168013
Clinical application
Peptide-targeted radionuclide therapy (PTRT) of advanced adenocarcinomas PMID 34168013
Theranostic pair
<a href="/tracers/ga68-fap2286/">ga68-fap2286</a>

Regulatory status

FDA
EMA (centralised)
Other approvals
Brand names

Clinical use

Typical injected activity
Uptake time

Reported in the literature. Not a dosing recommendation.

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
41599688
2026 Pharmaceuticals (Basel)
Manual synthesis≥ 93%FAP-228637261473
2023 Eur J Nucl Med Mol Imaging
177Lu-labeling was performed at different conditions, depending on the ligand (Supplementary Table 1).
36813980
2023 Eur J Nucl Med Mol Imaging
PiRoSyn
Sykam
>98%FAP-228634168013
2022 J Nucl Med
Automated labeling was performed using a PiRoSyn synthesis module (Sykam) (19).

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Notes

Added at stage 21 from therapy-discovered.xlsx (bulk PubMed search by isotope/therapy-type/known-agent, not individually researched yet) -- 10 articles found. Target/mechanism, clinical application, indications, approval and precursor fields still need per-agent research and are intentionally left empty. Diagnostic pair signal at discovery: YES - Ga-68. Compound class inferred from precursor name (not stated outright) -- PMID 37261473: 'cyclic peptide FAP-2286'. Stage set/updated at stage 23 from PMID 34168013: 'We present the first-in-humans results using 177Lu-FAP-2286 for peptide-targeted radionuclide therapy (PTRT).'.