Clinical Trials Directory

Trials / Terminated

TerminatedNCT00003524

Antineoplaston Therapy in Treating Patients With Stomach Cancer

Phase II Study of Antineoplastons A10 and AS2-1 In Patients With Adenocarcinoma of the Stomach

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
1 (actual)
Sponsor
Burzynski Research Institute · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Current therapies for Stomach Cancer provide very limited benefit to the patient. The anti-cancer properties of Antineoplaston therapy suggest that it may prove beneficial in the treatment of Stomach Cancer. PURPOSE: This study is being performed to determine the effects (good and bad) that Antineoplaston therapy has on patients with Stomach Cancer.

Detailed description

Stomach Cancer cancer patients receive gradually escalating doses of intravenous Antineoplaston therapy (Atengenal + Astugenal) until the maximum tolerated dose is reached. Treatment continues up to12 months in the absence of disease progression or unacceptable toxicity. OBJECTIVES: * To determine the efficacy of Antineoplaston therapy in patients with Stomach Cancer, 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 patients with Stomach Cancer. * 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.

Conditions

Interventions

TypeNameDescription
DRUGAntineoplaston therapy (Atengenal + Astugenal)Patients with Stomach Cancer will receive Antineoplaston therapy (Atengenal + Astugenal). The daily doses of A10 and AS2-1 are divided into six infusions, which are given at 4-hourly intervals. Each infusion starts with infusion of A10 and is immediately followed by infusion of AS2-1.

Timeline

Start date
1996-10-04
Primary completion
1998-08-24
Completion
1998-08-24
First posted
2003-01-27
Last updated
2017-09-29

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT00003524. Inclusion in this directory is not an endorsement.