Apatinib and Irinotecan in Treating Patients With Recurrent High-grade Glioma
- Sponsor
- The First People's Hospital of Lianyungang
- Study ID
- NCT02848794
- Phase
- PHASE1/PHASE2
- Status
- Unknown
Conditions
- High-grade Glioma
Eligibility Criteria
- Sex
- ALL
- Age
- 15 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib and Irinotecan — DRUGPatients were administered at apatinib (850mg po qd) and irinotecan(125mg/m2 d1,8) intravenously every three weeks for up to 6 cycles.Maintenance apatinib (500mg po qd) was administered until disease progression or unacceptable toxicity.
Study Details
The study is aimed to evaluate the efficacy and safety of Apatinib and Irinotecan in patients with recurrent high-grade glioma.
Key Dates
- Start date
- Jul 31, 2016
- Status verified
- Jun 2017
- Primary completion
- Jul 31, 2018
- Completion
- Jul 31, 2018
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Apatinib+IrinotecanApatinib and irinotecan in treating patients with recurrent high-grade glioma,who have progressed on temozolomide, or radiotherapy alone, or combined with chemotherapy within 3 months after surgery .
Primary Outcome Measure
Progression-Free Survival (PFS) [ Time Frame: From enrollment to progression of disease. Estimated about 6 months ]
Central Contacts
- Xiaodong Jiang, Doctor+86018961326201
- Tao YANG, Master+86018961327792
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