Drugs / AAA617
AAA617
Trials 7
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 11 trial | ||||||
| Phase 1 | NCT06531499 | Nov 2024 → Nov 2028 expected | prostate carcinoma | Novartis Pharmaceuticals | Recruiting | No outcome recorded |
| Phase 24 trials | ||||||
| Phase 2 | NCT06894511 | Sep 2025 → Oct 2026 expected | prostate carcinoma | Novartis Pharmaceuticals | Active not recruiting | No outcome recorded |
| Phase 2 | NCT07047118 | Jul 2025 → Jul 2027 expected | castration-resistant prostate carcinoma | Novartis Pharmaceuticals | Active not recruiting | No outcome recorded |
| Phase 2 | NCT06004661 | Apr 2024 → Dec 2026 expected | castration-resistant prostate carcinoma | Novartis Pharmaceuticals | Active not recruiting | No outcome recorded |
| Phase 2 | NCT05849298 | Jan 2024 → Dec 2026 expected | prostate neoplasm | Novartis Pharmaceuticals | Active not recruiting | No outcome recorded |
| Phase 31 trial | ||||||
| Phase 3 | NCT05939414 | Mar 2024 → Apr 2028 expected | prostate carcinoma | Novartis Pharmaceuticals | Recruiting | No outcome recorded |
| Phase 41 trial | ||||||
| Phase 4 | NCT05803941 | Aug 2023 → Jul 2033 expected | prostate cancer | Novartis Pharmaceuticals | Recruiting | No outcome recorded |
| Comparator or background therapy1 trial | ||||||
| Phase 3 | NCT06855277 Comparator | Jul 2025 → Sep 2028 expected | prostate cancer | Novartis Pharmaceuticals | Recruiting | No outcome recorded |
Evidence & citations 4 cited values
Every value below carries the sentence it was read from. 8 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | AAA617 | “The trial doctor will select either an ARPI of enzalutamide or abiraterone, or a taxane based chemotherapy of docetaxel or cabazitaxel or \[177Lu\]Lu-PSMA-617 (AAA617).” NCT06855277 ↗ |
| Known as | [177Lu]Lu-PSMA-617 (AAA617) | “[177Lu]Lu-PSMA-617 (AAA617)” NCT06855277 ↗ |
| Known as | lutetium (177Lu) vipivotide tetraxetan | “This study will address health authorities' requests to determine whether moderate and severe renal impairment have an impact on the biodistribution, dosimetry and safety of...” NCT06004661 ↗ |
| Route | Intravenous | “Administration intravenously once every 6 weeks (1 cycle) for 6 cycles” NCT05849298 ↗ |