Study of Convection-Enhanced, Image-Assisted Delivery of Liposomal-Irinotecan In Recurrent High Grade Glioma
Part of paid clinical trials in San Francisco, California.
- Sponsor
- University of California, San Francisco
- Study ID
- NCT02022644
- Phase
- PHASE1
- Status
- Completed
Conditions
- High Grade Glioma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- nanoliposomal irinotecan — DRUGThe drug named here (nanoliposomal irinotecan) will be used in varying amounts, based on tumor volume.
Study Details
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).
Key Dates
- Start date
- Oct 23, 2014
- Status verified
- Jun 2023
- Primary completion
- Dec 31, 2020
- Completion
- May 31, 2023
Study Design
- Enrollment
- 18 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Group 1 - 20 mgTumor diameter: 1 cm, Tumor volume: \~0.5cm3, Infusion Volume: 2-3 ml, Irinotecan conc.: 20 mg/ml, Infusion time: 6-24 hours, no more than 48
- Experimental: Group 2 - 40 mgTumor diameter: 2 cm,Tumor volume: \~4.1cm3, Infusion Volume: 3-4 ml, Irinotecan conc.: 40 mg/ml, Infusion Time: 6-24 hours, no more than 48
- Experimental: Group 3 - 140 mgTumor diameter: 3 cm, Tumor volume: \~14cm3, Infusion Volume: 6-7 ml, Irinotecan conc.: 140 mg/ml, Infusion Time: 6-24 hours, no more than 48
- Experimental: Group 4 - 340 mgTumor diameter: 4 cm, Tumor volume: \~34cm3, Infusion Volume: ≤17 ml, Irinotecan conc.: 340 mg/ml, Infusion Time: 6-24 hours, no more than 48
- Experimental: Group 5 - 40 mgTumor diameter: 1 cm, Tumor volume: \~0.5cm3, Infusion Volume: 2-3 ml, Irinotecan conc.: 40 mg/ml, Infusion Time: 6-24 hours, no more than 48
- Experimental: Group 6 - 80 mgTumor diameter: 2 cm, Tumor volume: \~4.1cm3, Infusion Volume: 3-4 ml, Irinotecan conc.: 80 mg/ml, Infusion Time: 6-24 hours, no more than 48
- Experimental: Group 7 - 280 mgTumor diameter: 3 cm, Tumor volume: \~14cm3, Infusion Volume: 6-7 ml, Irinotecan conc.: 280 mg/ml, Infusion Time: 6-24 hours, no more than 48
- Experimental: Group 8 - 680 mgTumor diameter: 4 cm, Tumor volume: \~34cm3, Infusion Volume: ≤17 ml, Irinotecan conc.: 680 mg/ml, Infusion Time: 6-24 hours, no more than 48
Primary Outcome Measure
Maximum tolerated dose [ Time Frame: 30 days post-infusion ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California, San Francisco | San Francisco | California | 94143 | - |
Find similar trials in San Francisco, CA
By research site
Related Studies
- A Study to Learn About the Study Medicine Called PF-07799544 as Monotherapy or in Combination in People With Advanced Solid TumorsPHASE1 · Recruiting · Pfizer · Birmingham, Alabama
- DB107-RRV, DB107-FC, and Radiation Therapy With or Without Temozolomide (TMZ) for High Grade GliomaPHASE1/PHASE2 · Recruiting · University of California, San Francisco · Los Angeles, California
- Dabrafenib and/or Trametinib Rollover StudyPHASE4 · Recruiting · Novartis Pharmaceuticals · Scottsdale, Arizona
- C7R-GD2.CAR T Cells for Patients With GD2-expressing Brain Tumors (GAIL-B)PHASE1 · Recruiting · Baylor College of Medicine · Houston, Texas