Tracers / [177Lu]Lu-LuPSMA-617

[177Lu]Lu-LuPSMA-617

Also written as [Lu-177]LuPSMA-617
Radionuclide
Lu-177 t½ 9584.6 min
Modality
Therapy
Production route
Stage
approved
Syntheses indexed
8

What it is

Compound class
PSMA-617, urea-based PSMA-targeting ligand (Glu-urea-Lys pharmacophore) labeled with Lutetium-177
Target / mechanism
Targets prostate-specific membrane antigen (PSMA) PMID 36288537
Clinical application
Radioligand therapy for metastatic castration-resistant prostate cancer (mCRPC) PMID 36288537
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 synthesis>95%PSMA-617 ligand
MedKoo Biosciences
40397137
2025 Eur J Nucl Med Mol Imaging
The PSMA-617 ligand (MedKoo Biosciences) was prepared as described by Stenberg et al.
Manual synthesis≥99%≥99%PSMA-617
ABX
37889298
2024 Eur J Nucl Med Mol Imaging
The administered [177Lu]Lu-PSMA-617 was synthesized in accordance with standard procedures as described by Kratochwil et al. [30]. — Yield and purity of the radio tracer were ≥99%.
PSMA-61736288537
2022 Oncologist
Manual synthesisPSMA-61735807385
2022 Molecules
For the radiolabeling of [177Lu]Lu-PSMA-I&T, a manual synthesis was used.
Scintomics GRP / GRP-3V
Scintomics
vendor cassettenone>90 %92 %PSMA-617
ABX
27090254
2016 EJNMMI Res
Both kinds of synthesis was carried out with a Scintomics GRP synthesizer, sterile single use cassettes and the standard synthesis sequences for 68Ga-peptides respective therapeutic peptides. — The labelling to 177Lu-PSMA-617 was quantitative, there for the yield was >90 %
41642049
2026 Clin Nucl Med
39978808
2025 J Nucl Med
PSMA-61737670407
2023 J Med Chem

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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 36288537: 'This has ultimately led to the approval of this therapy by the US Food and Drug Administration (FDA) on March 23 2022.'.