Tracer library / [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
- Clinical research
- Syntheses indexed
- 2
What it is
Published syntheses
| Module | Cassette | Purification | Yield % | RCP % | Precursor / supplier | Source |
|---|---|---|---|---|---|---|
| Manual synthesis | — | none | — | >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-LM3 | 34625828 2022 Eur J Nucl Med Mol Imaging |
Clinical literature
Clinical studies in the indexed corpus, ordered by design (multicentre, prospective, retrospective, others, case reports last) and then by year. Titles and links only, as published; this is not a summary of the evidence.
- Targeted β--Particle Plus Conversion and Auger-Electron Therapy with 161Tb-Labeled Somatostatin Receptor Antagonist DOTA-LM3: A Phase 0 Study.2026 · J Nucl Med · Prospective · Phase 0
Precursor
- Common precursor
- —
- Suppliers seen in the literature
- —
- Cited suppliers in indexed syntheses
- CSBio
- Typical final purification
- —
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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.'. | Stage 30 (2026-09-18): Stage was 'Phase 0 clinical study'; normalised to 'Clinical research', original wording kept here.