Sintilimab in Combination With Bevacizumab and Temozolomide in Recurrent Glioblastoma (GBM) Patients
- Sponsor
- Zhujiang Hospital
- Study ID
- NCT05638451
- Phase
- PHASE2
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Sintilimab plus Bevacizumab and Temozolomide — DRUG200mg Sintilimab plus 10mg/kg Bevacizumab very 3 weeks 200 mg/m2/day Temozolomide on days 1-5 out of a 28 days schedule
Study Details
The purpose of this study is to evaluate the efficacy and safety of Sintilimab in combination with Bevacizumab and Temozolomide in subjects with recurrent glioblastoma.
Key Dates
- First listed
- Dec 6, 2022
- Start date
- May 1, 2023
- Status verified
- Jun 2023
- Primary completion
- Dec 30, 2024
- Completion
- Dec 30, 2024
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Sintilimab and Bevacizumab and Temozolomidesingle arm study
Primary Outcome Measure
Progression free survival rate at 6 months [ Time Frame: Up to two years ]
Central Contacts
- Junde Zhang, MD13002087575
- Yujing Tan, PHD13560347303
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