CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 9 enrolled
Drug / intervention
lapatinib ditosylate +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00107003
NCT00107003Phase 2Completed

A Biomarker and Phase II Study of GW572016 in Recurrent Malignant Glioma

National Cancer Institute (NCI)·interventional·Posted Apr 4, 2005·Updated Jul 5, 2018

In Brief

A Phase 2 clinical trial evaluating lapatinib ditosylate, Adjuvant therapy, and 2 other interventions for Glioma and 5 related conditions. Completed, enrolled 9 participants across 1 site.

Detailed Summary

This study will examine whether an experimental drug called GW572016 can delay tumor growth in patients with glioblastoma multiforme (GMB, a malignant brain tumor). GW572016 is believed to affect cancer cell function by interfering with the internal signaling needed for the cancer to grow. The study will also determine whether the presence of specific proteins in the tumor can predict what effects GW572016 will have on the tumor. Patients 18 years of age and older with GMB whose brain tumor does not respond to standard medical treatment and who can undergo surgery for their tumor may be eligible for this study. Candidates are screened with a physical examination and neurocognitive examination, blood tests, electrocardiogram (EKG), echocardiogram (ultrasound test of heart function) or MUGA scan (nuclear medicine test of heart function), magnetic resonance imaging (MRI) of the head, and computed tomography (CT) of the head. CT uses x-rays and MRI uses a magnetic field and radio waves to show brain structure. Participants undergo the following tests and procedures: * MRI and blood tests before surgery. * Surgery to remove the brain tumor. * Follow-up MRIs every 8 weeks after surgery. * Follow-up echocardiograms or MUGA scans every 8 weeks after surgery. * GW572016 treatment starting 7-10 days before surgery and continuing until the patient or doctor decides it is in the patient's best interest to stop it or until the tumor worsens. (The drug is stopped temporarily for surgery and a healing period after surgery.) * Blood tests every 2 weeks to evaluate the effects of GW572016 on the body. * Blood test before the first GW572016 treatment and at the time of surgery to assess the effect of the drug on the cells and to determine how much drug is present in the blood at the time of surgery. Participants are followed in clinic at least monthly while taking GW572016. While on treatment they keep a diary documenting their daily treatments. The diary is collected at the monthly follow-up exams. After the treatment ends, patients are contacted periodically by the research staff for the rest of their lives to follow the long-term effects of the study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedApr 4, 2005
Enrollment StartMar 30, 2005
Primary CompletionDec 5, 2007
Study CompletionNov 30, 2012
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 21.2 years ago

Interventions

lapatinib ditosylatedrug

Adjuvant therapyprocedure

Conventional surgeryprocedure

Neoadjuvant therapyprocedure