Clinical trial · Interventional
Treatment of Recurrent Glioblastoma With Fractionated Radiotherapy Combined With Cadonilimab
NCT05737368CI-TRIAL-00064122unknownPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- 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)
The purpose of this study is to evaluate the safety and effectiveness in the treatment of recurrent glioblastoma with Cadonilimab combined with fractionated radiotherapy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Recurrent Glioblastoma | Glioblastoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| cadonilimab | Drug | — | UNRESOLVED |
| fractionated radiotherapy | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Patients will receive the treatment of fractionated radiotherapy and Cadonilimab
- description
- fractionated radiotherapy (500cGy \*5F, 600cGy\*5F, 350cGy\*10F, according to the tumor volume); within 14 days after receiving radiotherapy, Cardunizumab (10mg/kg, Q3W, d1)
- interventionNames
- Radiation: fractionated radiotherapy
- Drug: cadonilimab
Primary outcomes (1)
- measure
- Incidence and severity of adverse events (AEs)
- timeFrame
- 3 months after treatment
Secondary outcomes (5)
- measure
- Local control rate (LC)
- timeFrame
- from date of enrollment to date of first documented local progression. Assessed up to 6 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. . Written and signed informed consent. 2. . Male or female, age≥ 18 and ≤ 75 years old on day of signing informed consent. 3. Epitentorial glioblastoma confirmed by pathology; Diagnosis of recurrence through clinical imaging evidence. 4. The maximum diameter of recurrent tumor is less than 6 cm. 5. Concurrent radiotherapy and chemotherapy with standard STUP treatment scheme in the past. 6. The interval from the last radiotherapy is more than 6 months. 7. KPS (Karnofsky function status score)\>60. Exclusion Criteria: 1. Prior use of investigational products or devices within 4 weeks prior to the first administration of the study treatment. 2. Concurrent enrollment into another clinical study, except the study belongs to investigational, non-interventional studies or the follow-up period of interventional studies. 3. Multiple malignant gliomas. 4. Subtentorial glioblastoma or Extracranial metastatic lesions. 5. Active autoimmune diseases. 6. Known history of primary immunodeficiency virus infection or known history of testing positive for human immunodeficiency virus (HIV).
References
Publications (0)
Data not yet available
No reference posted for this study.