Tracers / [161Tb]Tb-DOTA-LM3

[161Tb]Tb-DOTA-LM3

Also written as [Tb-161]Tb-DOTA-LM3
Radionuclide
Tb-161 t½ 9907.2 min
Modality
Therapy
Production route
Stage
Phase 0 clinical study
Syntheses indexed
3

What it is

Compound class
DOTA-conjugated somatostatin receptor antagonist peptide
Target / mechanism
Somatostatin receptor (SSTR) antagonist PMID 39046521
Clinical application
Peptide receptor radionuclide therapy of somatostatin receptor-positive neuroendocrine tumours PMID 41381241
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
SPEat least 95%DOTA-LM341381241
2026 J Nucl Med
[161Tb]Tb-DOTA-LM3 was manufactured by radiolabeling 100 µg of DOTA-LM3 with [161Tb]TbCl3 using an automated synthesis module.
Manual synthesisnone>98%DOTA-LM3
CSBio, California, US
39046521
2024 Eur J Nucl Med Mol Imaging
DOTA-LM3 (CSBio, Silicon Valley Menlo Park, California, United States) and DOTATATE (Bachem, Bubendorf, Switzerland) were labeled with terbium-161 or lutetium-177 at a molar activity of up to 100 MBq/nmol using standard labeling conditions as previously reported
≥ 98%DOTA-LM334625828
2022 Eur J Nucl Med Mol Imaging

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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) -- 4 articles found. 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 41381241: 'DOTA-LM3'. Stage set/updated at stage 23 from PMID 41381241: 'A Phase 0 Study.'.