TH-302 in Combination With Bevacizumab for Glioblastoma
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- The University of Texas Health Science Center at San Antonio
- Study ID
- NCT02342379
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Bevacizumab — DRUG10mg/kg
- TH-302 — DRUG670mg/m2
Study Details
Dual center, single arm, two-stage, non-blinded, prospective study of combination therapy bevacizumab at 10mg/kg and TH-302 at 670mg/m2 every 2 weeks (6 week cycle) until disease progression.
Key Dates
- First listed
- Jan 19, 2015
- Start date
- May 31, 2015
- Status verified
- Apr 2020
- Primary completion
- Jan 4, 2019
- Completion
- Dec 4, 2019
Study Design
- Enrollment
- 35 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Bevacizumab and TH-302Patients will be treated with combination of bevacizumab and TH-302.
Primary Outcome Measure
Number of Patients With Adverse Events [ Time Frame: 4 months ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Dana-Farber Cancer Institute | Boston | Massachusetts | 02215 | - |
| University of Texas Health Science Center San Antonio at the Cancer Therapy and Research Center | San Antonio | Texas | 78229 | - |
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