Clinical trial · Interventional
Neoadjuvant Carilizumab and Apatinib for Recurrent High-Grade Glioma
A Study to Evaluate the Safety and Efficiency of Using the Neoadjuvant Therapy With Carilizumab and Apatinib in Patients With Recurrent High-Grade Glioma ：A Prospective, Randomized Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
GBM is the most common intracranial tumor in adults, accounting for about 40% of all primary intracranial tumors.Although surgery, radiotherapy and chemotherapy have been used, the prognosis of glioma patients is still very poor. The study aim to Evaluate the Safety and efficiency of Using the neoadjuvant therapy with Carilizumab and Apatinib in patients with Recurrent High-Grade Glioma.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Apatinib | — | UNRESOLVED | — |
| Carilizumab | — | UNRESOLVED | — |
| Neoadjuvant Therapy | — | UNRESOLVED | — |
| Recurrent High-Grade Glioma | High-Grade Glioma, NOS | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PD-1 | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Neoadjuvant group
- description
- Patients need to treat with PD-1 and apatinib before surgery. Sequential therapy with PD-1 and apatinib when patients accepted surgery.
- interventionNames
- Biological: PD-1
- type
- EXPERIMENTAL
- label
- Adjuvant group
- description
- Before surgery, patients no need to treat with PD-1 and apatinib. Sequential therapy with PD-1 and apatinib when patients accepted surgery.
- interventionNames
- Biological: PD-1
Primary outcomes (1)
- measure
- Overall survival (OS)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Written informed consent. 2. Age 18-70 years old, both male and female. 3. After biopsy or surgery, the postoperative pathological diagnosis was WHO III-IV glioma. 4. Patients in whom surgery can be safely delayed for a minimum period of 2 weeks following the administration of the first dose of nivolumab, in the opinion of the investigator. 5. KPS score ≥60； 6. Life expectancy \>12 weeks. 7. Adequate organ function defined by: 1. HGB≥110g/L； 2. WBC≥3.0×109/L；NEUT≥1.5×109/L； 3. PLT ≥75×109/L； <!-- --> 1. BIL≤1.5ULN； 2. ALT and AST≤2.0×ULN； 3. creatinine \< 1.5 x ULN or estimated creatinine clearance≥50ml/min（using the Cockcroft-Gault formula） Exclusion Criteria: 1. Presence of extracranial disease. 2. Previous treatment with a PD-1, PDL-1 or CTLA-4，VEGFR targeted therapy. 3. Pregnant or breastfeeding patients. 4. Known history of testing positive for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS). Routine testing is not required. 5. Positive tests for hepatitis B virus surface antigen (HBV sAg) or hepatitis C virus ribonucleic acid (HCV RNA) indicating active or chronic infection. 6. History of allergy to study drug components or of severe hypersensitivity reactions to any monoclonal antibodies. 7. Known drug or alcohol abuse.
References
Publications (0)
Data not yet available