Prescribing information for LUTATHERA® (lutetium (177Lu) oxodotreotide) (external link)
Prescribing information for Pluvicto®▼ (lutetium (177Lu) vipivotide tetraxetan) (external link)
Prescribing information for Locametz®▼ (gozetotide) (external link)
Prescribing information for SomaKit TOC® (edotreotide) (external link)
The science of RLT and Novartis RLT services
RLT is an innovative approach to cancer treatment that delivers targeted ionising radiation directly to tumour cells, wherever they are in the body.1,2
Designed for precision
RLT is a precision-medicine approach that recognises and directly treats a disease by using specific biomarkers expressed on the surface of target cells and delivering radiation with a cytotoxic effect.1,2
Using this approach, RLTs can be engineered to specifically target markers expressed in a variety of cancers, including prostate and neuroendocrine tumours.1,2





From production to patient – powered by manufacturing expertise
We source scarce materials years before they are required, activate them in highly regulated sterile environments, and transfer the radiopharmaceuticals from production to eligible patients.
Our vision for automated lines and expanded capacity will set benchmarks in the manufacturing of RLTs.
Learn how we ensure every dose is delivered with precision from production to eligible patients
Learn more about prostate cancer
Learn more about scanning for PSMA
Learn more about neuroendocrine tumours
DNA, deoxyribonucleic acid; PSMA, prostate-specific membrane antigen; RLI, radioligand imaging; RLT, radioligand therapy.
References
George SJ & Samuel EJJ. Front Chem 2023;11:1218670.
Sgouros G, et al. Nat Rev Drug Discov 2020;19(9):589–608.
Duan H, et al. Nanotheranostics 2022;6(1):103–117.
Yordanova A, et al. Onco Targets Ther 2017;10:4821–4828.
Van der Heide CD & Dalm SU. Eur J Nucl Med Mol Imag 2022;49(13):4616–4641.
Locametz®▼ (gozetotide) Summary of Product Characteristics.
SomaKit TOC® (edotreotide) Summary of Product Characteristics.
UK | December 2025 | FA-11482672
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report, or alternatively email [email protected] or call 01276 698370.