drugset / Trial / NCT02022644
Study of Convection-Enhanced, Image-Assisted Delivery of Liposomal-Irinotecan In Recurrent High Grade Glioma
Phase 1
Completed
18 enrolled
University of California, San Francisco
Ipsen · collabNational Cancer Institute (NCI) · collab
Non-randomizedSingle-groupOpen-labelTreatment
Summary
This is a single center, dose-toleration study designed to investigate and determine the maximum tolerated dose of nanoliposomal irinotecan in adults with recurrent high-grade glioma when administered directly into the tumor using a process called convection-enhanced delivery (CED).
Timeline
- Start
- 2014-10-23
- Primary completion
- 2020-12-31
- Completion
- 2023-05-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Nanoliposomal Irinotecan | Unknown | 20 mg | Other |
| Subject | Nanoliposomal Irinotecan | Unknown | 40 mg | Other |
| Subject | Nanoliposomal Irinotecan | Unknown | 80 mg | Other |
| Subject | Nanoliposomal Irinotecan | Unknown | 140 mg | Other |
| Subject | Nanoliposomal Irinotecan | Unknown | 280 mg | Other |
| Subject | Nanoliposomal Irinotecan | Unknown | 340 mg | Other |
| Subject | Nanoliposomal Irinotecan | Unknown | 680 mg | Other |