drugset / Trial / NCT03647657
177Lu-PP-F11N in Combination With Sacubitril for Receptor Targeted Therapy and Imaging of Metastatic Thyroid Cancer
Phase 0
Completed
8 enrolled
University Hospital, Basel, Switzerland
Center for Proton Therapy, Paul Scherrer Institute, Villigen,Switzerland · collabKrebsforschung Schweiz, Bern, Switzerland · collabUniversity Hospital Freiburg · collabUniversity Hospital, Zürich · collab
RandomizedCrossoverOpen-labelBasic science
Summary
The purpose of this study is to determine the use of 177Lu-PP-F11N for imaging and therapy of patients with advanced medullary thyroid carcinoma (MTC). 177Lu-PP-F11N is a gastrin analogon, binding to cholecystokinin-2 receptors. This receptors show an overexpression on more than 90 % of medullary thyroid carcinomas.
Timeline
- Start
- 2018-12-13
- Primary completion
- 2021-12-14
- Completion
- 2021-12-14
Publications
- Results Sauter AW, Mansi R, Hassiepen U, Muller L, Panigada T, Wiehr S, Wild AM, Geistlich S, Behe M, Rottenburger C, Wild D, Fani M. Targeting of the Cholecystokinin-2 Receptor with the Minigastrin Analog 177Lu-DOTA-PP-F11N: Does the Use of Protease Inhibitors Further Improve In Vivo Distribution? J Nucl Med. 2019 Mar;60(3):393-399. doi: 10.2967/jnumed.118.207845. Epub 2018 Jul 12.
- Rottenburger C, Hentschel M, Furstner M, McDougall L, Kottoros D, Kaul F, Mansi R, Fani M, Vija AH, Schibli R, Geistlich S, Behe M, Christ ER, Wild D. In-vivo inhibition of neutral endopeptidase 1 results in higher absorbed tumor doses of [177Lu]Lu-PP-F11N in humans: the lumed phase 0b study. EJNMMI Res. 2024 Apr 6;14(1):37. doi: 10.1186/s13550-024-01101-w.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PP-F11N LUTETIUM | Protein / enzyme biologic | 1000 mbq | Intravenous |
| Subject | Sacubitril | Small molecule | 48.6 mg | Oral |