CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 12 enrolled
Drug / intervention
Capecitabine +1 moredrug
Likely dose
Bevacizumab 10 mg/kgfrom 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/NCT02669173
NCT02669173Phase 1Completed

Targeting Myeloid Derived Suppressor Cells in Recurrent Glioblastoma: Phase 0/1 Trial of Low Dose Capecitabine + Bevacizumab in Patients With Recurrent Glioblastoma

Case Comprehensive Cancer Center·interventional·Posted Feb 1, 2016·Updated Feb 23, 2026

In Brief

A Phase 1 clinical trial evaluating Capecitabine and Bevacizumab for Glioblastoma. Completed, enrolled 12 participants across 1 site.

Detailed Summary

This study involves participants with recurrent glioblastoma brain tumors (GBM). This means that a participant's brain tumor has either returned after being treated by a previous therapy, or has continued to progress despite being treated. The purpose of this study is to provide proof of concept that suppression of MDSCs (myeloid-derived suppressor cells) is feasible in patients with GBM. Rather than targeting tumor cells or immune checkpoints, which has been the focus of recent therapeutic efforts, direct targeting of MDSCs with low dose capecitabine has the potential to reverse the immunosuppressed microenvironment of GBM and thereby reduce tumors

Study Details

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

Timeline

Phase 1CompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 1, 2016
Enrollment StartOct 11, 2016
Primary CompletionJan 7, 2025
TodayJul 2, 2026
Enrollment to primary: 8.2 yearsPosted 10.4 years ago

Interventions

Capecitabinedrug

Drug given orally. Dose to be determined by phase 1 dose escalation, cycle length 28 days. Treatment until progression

Bevacizumabdrug

Drug given by IV, 10 mg/kg days 1, 15 every 28 days, until progression.