Clinical Trials Directory

Trials / Completed

CompletedNCT00003468

Antineoplaston Therapy in Treating Children With Low-Grade Astrocytoma

Phase II Study of Antineoplastons A10 and AS2-1 in Children With Low Grade Astrocytoma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
11 (actual)
Sponsor
Burzynski Research Institute · Academic / Other
Sex
All
Age
6 Months – 17 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Current therapies for children with low grade astrocytomas that have not responded to standard therapy provide limited benefit to the patient. The anti-cancer properties of Antineoplaston therapy suggest that it may prove beneficial in the treatment of children with low grade astrocytomas that have not responded to standard therapy PURPOSE: This study is being performed to determine the effects (good and bad) that Antineoplaston therapy has on children (\> 6 months of age) with low grade astrocytomas that has not responded to standard therapy.

Detailed description

OBJECTIVES: * To determine the efficacy of Antineoplaston therapy in children with low grade gliomas that has not responded to standard therapy, as measured by an objective response to therapy (complete response, partial response or stable disease). * To determine the safety and tolerance of Antineoplaston therapy in children with a brain tumor. OVERVIEW: This is a single arm, open-label study in which children with low grade astrocytomas that have not responded to standard therapy receive gradually escalating doses of intravenous Antineoplaston therapy (Atengenal + Astugenal) until the maximum tolerated dose is reached. Treatment continues for at least 12 months in the absence of disease progression or unacceptable toxicity. After 12 months, patients with a complete or partial response or with stable disease may continue treatment. To determine objective response, tumor size is measured utilizing MRI scans, which are performed every 8 weeks for the first two years, every 3 months for the third and fourth years, every 6 months for the 5th and sixth years, and annually thereafter. PROJECTED ACCRUAL: A total of 20-40 patients will be accrued to this study.

Conditions

Interventions

TypeNameDescription
DRUGAntineoplaston therapy (Atengenal + Astugenal)Children with a low grade astrocytoma that have not responded to standard therapy will receive Antineoplaston therapy (Atengenal + Astugenal).

Timeline

Start date
1996-07-01
Primary completion
2004-07-01
Completion
2004-07-01
First posted
2003-01-27
Last updated
2023-11-21
Results posted
2016-11-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00003468. Inclusion in this directory is not an endorsement.