Condition: Solid Tumor · Metastatic Cancer · Unresectable Solid Tumor · Sponsor: Spago Nanomedical AB
The purpose of this first-in-human (FIH) study is to determine the maximum tolerated dose (MTD) and to characterize the safety, tolerability, PK, and dosimetry profile of \[177Lu\]Lu-SN201 in adult participants with advanced solid tumors who have no standard of care treatment options. \[177Lu\]Lu-SN201 is a radiolabeled, nanomedical investigational medicinal product (IMP) whose mechanism of delivery is based on the Enhanced Permeability and Retention (EPR) effect.
This description comes directly from the study's public registry record.
Chief Development Officer · +46 46 81188 · info@spagonanomedical.se
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| Cancer Research South Adelaide | Adelaide, South Australia, Australia | Recruiting |
| St Vincent Hospital Melbourne | Melbourne, Victoria, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06184035