Tracers / [177Lu]Lu-BPAMD

[177Lu]Lu-BPAMD

Also written as [Lu-177]Lu-BPAMD
Radionuclide
Lu-177 t½ 9584.6 min
Modality
Therapy
Production route
Stage
Syntheses indexed
2

What it is

Compound class
DOTA-conjugated bisphosphonate
Target / mechanism
Bone-seeking bisphosphonate with hydroxyapatite affinity for skeletal targeting PMID 41900797
Clinical application
Theranostic pair
<a href="/tracers/ga68-bpamd/">ga68-bpamd</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 synthesisnone>98%>98%BPAMD
ABX
41900797
2026 Pharmaceutics
Briefly, 74 MBq of [177Lu]LuCl3 was added in an aqueous solution containing 100 µg of BPAMD in 0.5 mL of sodium acetate buffer (0.4 M, pH 4.5). — Both complexes achieved a radiochemical yield of greater than 98%.
almost quantitativeBPAMD25714451
2015 Cancer Biother Radiopharm
An automated synthesis unit was designed for the production of therapeutic doses of [(177)Lu]BPAMD up to 5 GBq. — A Kit formulation combining BPAMD, acetate buffer, and ethanol resulted in almost quantitative labeling yields.

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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) -- 1 articles found. Target/mechanism, clinical application, indications, approval and precursor fields still need per-agent research and are intentionally left empty. Diagnostic pair signal at discovery: YES - Ga-68. Compound class inferred from precursor name (not stated outright) -- PMID 41900797: 'The ligand (4-{[(bis(phosphonomethyl))carbamoyl]methyl}-7,10-bis(carboxymethyl)-1,4,7,10-tetraazacyclododec-1-yl) acetic acid (BPAMD) was purchased from ABX (Radeberg, Germany).'.