Drugs / 177Lu-FAP-2286
Trials 2
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 1/21 trial | ||||||
| Phase 1/2 | NCT04939610 | Jul 2021 → Jun 2026 overdue | cancer | Novartis Pharmaceuticals | Recruiting | No outcome recorded |
| Phase 21 trial | ||||||
| Phase 2 | NCT07434180 | Jun 2026 → Jun 2030 expected | cancer of unknown primary site | Peter MacCallum Cancer Centre, Australia | Not yet recruiting | No outcome recorded |
Evidence & citations 3 cited values
Every value below carries the sentence it was read from. 3 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | 177Lu-FAP-2286 | ClinicalTrials.gov intervention name — accepted as the source's own label NCT07434180 ↗ |
| Known as | [177Lu]Lu-FAP-2286 | “Phase I of the LuMIERE study (ClinicalTrials.gov, NCT04939610) investigated the safety of [177Lu]Lu-FAP-2286 (177Lu-FAP-2286) in heavily pretreated patients with advanced solid...” PMID 42223513 ↗ Jun 2026 |
| Route | Intravenous | “Patients with positive uptake of 68Ga-FAP- 2286 will receive a fixed dose of 177Lu-FAP-2286 IV administered every 6 weeks for a maximum of 6 doses.” NCT04939610 ↗ |