Clinical trial · Interventional
Nimotuzumab in Combined With Chemoradiotherapy to Treat the Newly Diagnosed Diffuse Intrinsic Pontine Glioma in Children
A Multicenter, Prospective, Open and Single Arm Clinical Study of Nimotuzumab Combined With Concurrent Radiochemotherapy in the Treatment of Newly Diagnosed Diffuse Intrinsic Pontine Glioma (DIPG) in Children
- 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)
This is a prospective, open-label, single arm, multicenter clinical study. The purpose of the study is to evaluate the clinical efficacy and safety of combination Nimotuzumab with concurrent radiochemotherapy in children with newly diagnosed diffuse intrinsic pontine glioma(DIPG).
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 |
|---|---|---|---|
| Diffuse Intrinsic Pontine Glioma | Diffuse Intrinsic Pontine Glioma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Nimotuzumab+CRT(concurrent IMRT and TMZ) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Experimental
- description
- Nimotuzumab+CRT(concurrent IMRT and TMZ)
- interventionNames
- Drug: Nimotuzumab+CRT(concurrent IMRT and TMZ)
Primary outcomes (1)
- measure
- Objective response rate #ORR# assessed by the Independent Review Committee
- timeFrame
- Up to 12 months
- description
- Proportion of patients with partial or complete response in tumor burden as defined by RECIST.
Secondary outcomes (3)
- measure
- 1-year overall survival
- timeFrame
- Up to 12 months
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 3 Years
- Maximum age
- 15 Years
Show eligibility criteria text
Inclusion Criteria: 1. Voluntary and sign a consent form; 2. Age 3-15 years old, gender unlimited; 3. Histology or imaging diagnosed as diffuse intrinsic pontine glioma, patients haven't received any anti-tumor treatment; 4. According to the RANO criteria, at least one measurable lesion; 5. Before enrollment, the results of laboratory examination are in accordance with: Blood routine test: platelet count ≥ 100 × 10\^9/L; absolute neutrophil count ≥ 1.5 × 10\^9/L or leukocyte count ≥ 3.0 × 10\^9/L; hemoglobin ≥ 90g/L; Blood biochemistry: aspartate aminotransferase#AST# ≤ 3 ×Upper Limit Of Normal#ULN#; alanine aminotransferase#ALT# ≤ 3 × ULN; total bilirubin ≤ 1.5 × ULN; serum creatinine ≤ 1.5 × ULN; 6. Lansky score ≥ 60; 7. Expected survival time ≥ 3 months; 8. Fertile subjects are willing to take contraceptive measures during the study period. Exclusion Criteria: 1. Recurrent DIPG; 2. Have received any other anti-tumor treatment for DIPG, including surgical treatment (except biopsy), chemotherapy, radiotherapy, targeted drugs, immunotherapy, etc; 3. Uncontrollable infection, epilepsy and / or hypertension and / or hyperglycemia; 4. Human immunodeficiency virus #HIV# infection or active hepatitis B infection or hepatitis C infection; 5. Active hemorrhage found by CT or MRI before inclusion and / or inability to carry out CT and MRI examination; 6. Major operation (except biopsy) were performed within four weeks before inclusion; 7. Decompensated heart failure (NYHA grades III and IV), unstable angina, acute myocardial infarction, persistent and clinically significant arrhythmia within three months of inclusion; 8. Have other malignant tumor history; 9. Known allergy to Nimotuzumab, temozolomide or its analogues or any component of the prescription; 10. Unable to tolerate radiotherapy; 11. Other reasons that are not suitable to participate in this study according to the researcher's judgment.
References
Publications (0)
Data not yet available