MedPath

Study of intensive pediatric pharmacovigilance of nimotuzumab for the treatment of malignant glioma tumors.

Not Applicable
Completed
Conditions
Malignant gliomas
Registration Number
RPCEC00000183
Lead Sponsor
Centro de Inmunología Molecular (CIM)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
160
Inclusion Criteria

1. Children and adolescents between 2 and 19 years of age of btoh gender (male and female)
2. Diagnoses by histology/pathology documented or by images if stem tumor.
3. Life expectancy of at least 4 weeks.
4. Karnofsky / Lansky = 50%.

Exclusion Criteria

1. Participation in another trial.
2. Pregnant or breastfeeding.
3. Decompensated chronic disease.
4. Acute septic processes.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.