Ariceum Therapeutics to Present Outstanding New Preclinical Data at the Society of Nuclear Medicine and Molecular Imaging Annual Meeting 2024

Ariceum Therapeutics to Present Outstanding New Preclinical Data at the Society of Nuclear Medicine and Molecular Imaging Annual Meeting 2024

• SST2 antagonist, ²²⁵Ac-SSO110 (satoreotide), is multiple times more potent than SST2 agonist, ²²⁵Ac-DOTATATE
• Satoreotide demonstrated durable complete response in standard murine xenograft models of Small Cell Lung Cancer in animal models, versus tumor growth delay with ²²⁵Ac-DOTATATE

Berlin, Germany, 10 June, 2024 - Ariceum Therapeutics (Ariceum), a private biotech company developing radiopharmaceutical products for the diagnosis and treatment of certain hard-to-treat cancers, today announces that it will be presenting a poster demonstrating the efficacy of its somatostatin receptor 2 (SST2) antagonist, SS0110 (satoreotide), relative to SST2-targeting agonists, at this year’s Society of Nuclear Medicine and Molecular Imaging (SNMMI) Annual Meeting being held 8-11 June 2024 in Toronto, Canada. 

The poster presentation entitled ‘[²²⁵Ac]Ac-SSO110 and [¹⁷⁷Lu]Lu-SSO110 demonstrate significantly better efficacy than [²²⁵Ac]Ac-DOTA-TATE in the treatment of SST2-positive tumor xenografts’ compares satoreotide with the SST2 agonist, ²²⁵Ac-DOTATATE, and reveals that single doses of 20 MBq ¹⁷⁷Lu-satoreotide or 30 kBq ²²⁵Ac-satoreotide induce significantly better efficacy than a single dose of 30 kBq ²²⁵Ac-DOTATATE.  Most remarkably, 30 kBq ²²⁵Ac-satoreotide induced complete tumor regression in the NCI-H69 model, something not observed with the same or higher doses of ²²⁵Ac-DOTATATE.

These data highlight the significantly higher tumor uptake and longer tumor retention leading to a higher tumor to background and tumor to kidney ratios of satoreotide which translates into higher pre-clinical efficacy than SST2-targeting agonists when labelled with isotopes, ²²⁵Ac-satoreotide and ¹⁷⁷Lu-satoreotide. This demonstrates the potential for satoreotide to clinically outperform SST2-targeting agonists and strongly supports its further clinical development for the treatment of SST2 positive tumors such as Small Cell Lung Cancer (SCLC) and Merkel Cell Carcinoma (MCC).

Manfred Rüdiger, Chief Executive Officer at Ariceum Therapeutics, said: “With this significant data we demonstrate that satoreotide has the potential to be a game changer for the treatment of SCLC and MCC. Satoreotide is multiple times more potent than DOTATATE, irrespective of the isotope, and this confirms the superiority of SST2 antagonist over agonist. We look forward to presenting our findings at this year’s SNMMI meeting.”

Details of the poster presentation are as follow:

Title: [²²⁵Ac]Ac-SSO110 and [¹⁷⁷Lu]Lu-SSO110 demonstrate significantly better efficacy than [²²⁵Ac]Ac-DOTA-TATE in the treatment of SST2-positive tumor xenografts

Authors: Anika Jaekel, Prachi Desai, Germo Gericke, Manuel Sturzbecher-Hoehne, Dennis Mewis & Manfred Rüdiger

Presenter: Anika Jaekel, Senior Director, Head of Translational Biology and Non-Clinical Pharmacology at Ariceum Therapeutics

Session:  MTA07 POPs/Meet the Author: Oncology, Basic & Translational 2
Session Date and Time:  Monday, June 10, 2024, 10:00 - 11:15 DST
Abstract ID: 242038