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Completed

NCT Number: NCT00561873

Nimotuzumab in Children With HGG

Determination of efficiency of nimotuzumab in children with high grade glioma.

Completed

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Key information

Age range

3 year–20 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Bonn, Children's Medical Hospital

Bonn, 53113, Germany

About this study

High grade malignant gliomas are tumors grade III and IV according to WHO classification, that originate from oligodendroglia and astrocytes, where the latter are also known as anaplastic astrocytoma(WHO grade III) and glioblastoma(WHO grade IV). This also includes intrinsic pontine gliomas of adolescents, which are usually not documented histologically due to their localisation, but they have a similar clinical progress when compared to high grade malignant astrocytic tumors. Among various molecular alterations, malignant gliomas overexpress EGFR (epidermal growth factor) in nearly 50% of cases, which is particularly pronounced in glioblastoma.(Schlegel 2003) Standard therapy consists of radical surgery as extensive as medically responsible followed by radiotherapy dose of 60 Gy, which is aimed at the area with a safety margin. The long-term efficacy of additional chemotherapy has been a subject for controversy for several decades. The combination of all three treatment modalities in grade III tumors can lead to median survival times of 3-5 years in adults.

For this treatment group reports of 5 year recurrence free periods in 33-50% of cases have been reported in children and adolescents.

For glioblastoma(WHO grade IV) 5year recurrence free periods are 3% in elderly patients and 10-20% for adolescents.(Schlegel 2003) In German speaking territories chemotherapy with Cisplatin, Etoposid and Ifosfamid is used as a postoperative treatment option for adolescents and this disease.(Wolff HIT-GBM) In case of recurrence therapy choices are even more limited, thus if medically feasible the enrolment in clinical trials is an option.

In this study the aim is to use an antibody directed against the EGF-receptor to effect the proliferation of the tumor cells negatively. Pilot studies conducted in adults indicate that the median survival time for patients with malignant glioma can be prolonged by the antibody treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically confirmed diagnosis of high grade glioma (WHO III und IV) [not needed for intrinsic pontine glioma]
  • Progressive patients under primary therapy or first and second radiologically confirmed recurrence(MRI not older than 2 weeks) of high grade gliomas between the age of > 3 years < 20 years
  • Lack of curative standard therapy which is currently under investigation in a national GPOH-therapy optimization study
  • Sufficient haematological, renal and hepatic function (CTC Grad ≤ 2)
  • Disease measurable radiologicaly in at least one dimension
  • Life expectancy > 4 Weeks
  • Written declaration of consent of the parents/legal guardians and if possible of the child after prior information

Exclusion criteria

  • Curative therapy with an alternative method after diagnosis of progression and during this study
  • Prior administration of human or murine antibody
  • Pregnancy in girls of child-bearing age

Treatment and study plan

Primary outcomes

  1. Response rate according to RECIST criteria

    Time frame: week 8, week 21

Secondary outcomes

  1. Progress free interval, Toxicity according to CTC criteria, Symptom control

    Time frame: week 8, week 21

Sponsors and collaborators

Lead sponsor

Oncoscience AG

Industry

Collaborators

  • CRM Biometrics GmbH
  • Children's Medical Hospital, Medical School Hannover, Hannover, Germany
  • Children's Medical Hospital, University of Bonn, Germany
  • Children's Medical Hospital, University of Essen, Essen, Germany
  • Children's Medical Hospital, University of Homburg/Saar, Homburg/Saar, Germany
  • Dept. of Neuropediatrics and Muscle Disorders, University of Freiburg, Germany
  • Dept. of Statistics, University of Dortmund, Germany
  • Dr. von Haunersches Children's Medical Hospital, University of Munich, Germany
  • Heinrich-Heine University, Duesseldorf
  • University Hospital Augsburg
  • University of Bonn
  • University of Cologne
  • University of Regensburg
  • University of Wuerzburg
  • Universitätsklinikum Hamburg-Eppendorf

Registry information

Official study title

Phase-II-Study of Efficacy of OSAG 101 (Theraloc®) for Adolscent Patients With Recurrent High Grade Glioma

Important dates

Study start
2004
Study completion
2007
First posted
Nov 21, 2007
Registry last updated
Nov 21, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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