drugset / Trial / NCT06250244
177Lu-LNC1011 in Patients with Metastatic Castration-resistant Prostate Cancer
NaSingle-groupOpen-labelTreatment
Summary
This study employed an open-label, non-randomized design, representing the first human trial of its kind. It utilized a standard 3+3 dose-escalation approach, focusing on patients with metastatic castration-resistant prostate cancer, initiating treatment at a dose of 1.85 GBq over a 6-week period. Subsequent cohorts underwent sequential 50% dose escalations until the observation of dose-limiting toxicity (DLT).
Timeline
- Start
- 2023-05-01
- Primary completion
- 2025-04-01
- Completion
- 2025-10-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | 177Lu-LNC1011 | Other / unclassified | 1850 mbq | Intravenous |