Prescribing information (external link)

Image
Hero banner. LUTATHERA® (lutetium [177Lu] oxodotreotide) logo.
Image
Hero banner. LUTATHERA® (lutetium [177Lu] oxodotreotide) logo.

Mechanism of action

LUTATHERA® (lutetium [177Lu] oxodotreotide) is indicated for the treatment of unresectable or metastatic, progressive, well-differentiated (G1 and G2), somatostatin receptor (SSTR)-positive gastroenteropancreatic neuroendocrine tumours (GEP-NETs) in adults.1

LUTATHERA® Summary of Product Characteristics (SmPC) can be found here


LUTATHERA® delivers SSTR2-targeted radiation directly to overexpressing malignant cells of GEP-NETs1

Based on pre-clinical data.

GEP-NETs strongly overexpress SSTR22

  • With a high affinity for SSTR2, LUTATHERA® is designed to deliver beta radiation directly to tumour cells, disrupting them from within1

  • The beta radiation is mostly contained within the tumour, limiting damage to neighbouring healthy cells1

Image
Mechanism of action graphic in 4 stages detailing how LUTATHERA® is designed to deliver beta radiation directly to tumour cells, disrupting them from within.1

Stage 1

LUTATHERA® is infused into the bloodstream, where it targets and binds to malignant cells overexpressing SSTR2.1

Stage 2

LUTATHERA® is then internalised into the cell.3

Stage 3

In the cell, it delivers beta radiation, with an average tissue penetration of 0.67mm.1

Stage 4

The radiation disrupts the targeted tumour cell from within, with a limited effect on neighbouring normal cells.1




GEP-NET, gastroenteropancreatic neuroendocrine tumour; RLT, radioligand therapy; SmPC, summary of product characteristics; SSTR, somatostatin receptor.

References

  1. LUTATHERA® Summary of Product Characteristics.

  2. Thundimadathil J. J Amino Acids 2012;2012:967347.

  3. Hennrich U & Kopka K. Pharmaceuticals (Basel) 2019;12(3):114.

 

UK | December 2025 | FA-11462531-1

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.