Tracers / [177Lu]Lu-BL02

[177Lu]Lu-BL02

Also written as [Lu-177]Lu-BL02
Radionuclide
Lu-177 t½ 9584.6 min
Modality
Therapy
Production route
Stage
preclinical study
Syntheses indexed
1

What it is

Compound class
CXCR4-targeting radioconjugate derived from LY2510924 (CXCR4 antagonist peptide/small molecule)
Target / mechanism
CXCR4 antagonist targeting CXCR4-expressing tumor cells PMID 42653659
Clinical application
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 synthesiscustom manifoldSPE>99%>99%BL02
Pepmic Co., Ltd., Suzhou, China
42653659
2026 Pharmaceuticals (Basel)
[177Lu]Lu-BL02 and [161Tb]Tb-BL02 were manually labeled with radiochemical conversions (RCC) exceeding 99% for both tracers on iTLC. — were manually labeled with radiochemical conversions (RCC) exceeding 99% for both tracers on iTLC

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Notes

Added at stage 22: promoted from 'Reported once' (single-article, no diagnostic pair at discovery) because a full-text synthesis with extracted data exists in parsed-therapy.xlsx -- PMID(s): 42653659. 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 42653659: 'In vivo biodistribution and pharmacokinetics were evaluated in MM.1S xenograft mouse models, supported by longitudinal SPECT imaging.'. | Stage 28: added indication(s) onc-myeloma from consolidated missing-rubric review.