Tracers / [177Lu]Lu-LNC1010

[177Lu]Lu-LNC1010

Also written as [Lu-177]Lu-LNC1010; Lu-177-LNC1010
Radionuclide
Lu-177 t½ 9584.6 min
Modality
Therapy
Production route
Stage
first-in-human
Syntheses indexed
1

What it is

Compound class
SSTR2-targeting somatostatin analog peptide with Evans blue albumin-binding moiety (long-acting somatostatin analog)
Target / mechanism
SSTR2 agonist (somatostatin receptor subtype 2) PMID 40177560
Clinical application
Peptide receptor radionuclide therapy (PRRT) in patients with advanced/metastatic neuroendocrine tumors PMID 40177560
Theranostic pair

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 synthesisLNC101040177560
2025 Acta Pharm Sin B
370–740 MBq 177LuCl3 was mixed with LNC1010 (100–200 μg) and diluted with 0.2 mL of 0.5 mol/L NaOAc (pH = 5.5) and heated reaction at 95 °C for 30 min.

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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) -- 2 articles found. Target/mechanism, clinical application, indications, approval and precursor fields still need per-agent research and are intentionally left empty. Stage set/updated at stage 23 from PMID 40177560: 'we presented the first-in-human dose escalation study of 177Lu-LNC1010 in patients with advanced/metastatic NETs'.