Thank you! We will contact you soon.

Close

Radiopharmaceuticals

We deliver ready-for-injection radiopharmaceuticals on a weekly basis throughout the Nordic region

LUTATHERA

LUTATHERA®, 370 MBq/mL, solution for infusion is a ready-to-use product, indicated for the treatment of resectable or metastatic, progressive, well differentiated (G1 and G2), somatostatin receptor positive gastroenteropancreatic neuroendocrine tumors (GEP NETs) in adults.

The pivotal phase III study NETTER-1 compared 177Lu-DOTATATE and octreotide LAR 60 mg (double label dose) in patients with locally advanced or metastatic inoperable, grade 1 or grade 2 neuroendocrine tumors of the small intestine, progressing under treatment with octreotide LAR 20-30 mg every 21 to 28 days. The study showed a statistically significant 82% reduction in the risk of progression or death (Median PFS: octreotide LAR, 8.5 months LUTATHERA®, not reached. Hazard ratio: 0.18 (95% CI: [0.11-0.29] p<0.0001).

In the LUTATHERA® arm, patients also experienced an overall response rate of 18% (vs 3% in comparator arm p=0.0008) which is rarely seen with systemic therapies in the NETs population. LUTATHERA® demonstrates a favorable safety profile, with rare clinically relevant findings.

For more information see Summary of product characteristics (SmPC).

http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/004123/human_med_002163.jsp&mid=WC0b01ac058001d124

FDG (Fludeoxyglucose [18F])

This medicinal product is for diagnostic use only. Fludeoxyglucose (18F) is intended for use with positron emission tomography (PET). We deliver FDG from the cyclotron in Berlin, and it is available in Sweden only. FDG Eckert & Ziegler is a registered radiopharmaceutical since 2008