Tracers / [177Lu]Lu-eFAP-6

[177Lu]Lu-eFAP-6

Also written as [Lu-177]Lu-eFAP-6
Radionuclide
Lu-177 t½ 9584.6 min
Modality
Therapy
Production route
Stage
preclinical study
Syntheses indexed
1

What it is

Compound class
FAP-targeting DOTA-conjugated small molecule (quinolinoyl-glycyl-2-cyanopyrrolidine derivative)
Target / mechanism
Fibroblast activation protein (FAP) PMID 39073475
Clinical application
Theranostic pair
<a href="/tracers/in111-efap6/">in111-efap6</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
Manual synthesis>95%>95%eFAP-639073475
2024 EJNMMI Radiopharm Chem
Labeling reactions were performed in a solution containing sodium acetate (1 µL, 2.5 M), ascorbic and gentisic acids (10 µL, 50 mM), ethanol (10 µL), and complemented with Milli-Q water. — Radiolabeling of eFAP-6 with 111-indium and 177-lutetium was performed successfully with high radiochemical yield and purity (> 95%).

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Notes

Added at stage 22: promoted from 'Reported once' (single-article, no diagnostic pair at discovery) because a full-text synthesis with extracted data exists in parsed-therapy.xlsx -- PMID(s): 39073475. Target/mechanism, clinical application, indications, approval and precursor fields still need per-agent research and are intentionally left empty. Compound class inferred from precursor name (not stated outright) -- PMID 39073475: 'eFAP-6 (1 nmol), 50 MBq [111In]InCl3 (Curium Pharma, Petten, The Netherlands) or 13–20 MBq [177Lu]LuCl3'. Stage set/updated at stage 23 from PMID 39073475: 'In vitro and in vivo analyses of eFAP: a novel FAP-targeting small molecule for radionuclide theranostics and other oncological interventions.'.