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NCT01891747 · ClinicalTrials.gov registry record · Phase 1

A Phase I Study of High-dose L-methylfolate in Combination With Temozolomide and Bevacizumab in Recurrent High Grade Glioma

A Phase 1 study, sponsored by Vanderbilt-Ingram Cancer Center.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target

NCT01891747 is a Phase 1 study that has completed, run by Vanderbilt-Ingram Cancer Center. The registered enrollment target is 14 participants.

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The verdict

NCT01891747, a Phase 1 study, has completed, sponsored by Vanderbilt-Ingram Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target

Study Summary

This is a Phase I/II non-randomized prospective study of high-dose L-methylfolate in combination with bevacizumab and temozolomide in patients with recurrent high-grade glioma. The primary objective of this phase II trial is to determine whether the addition of high-dose L-methylfolate to bevacizumab and temozolomide therapy improves progression-free survival (PFS) compared to previously reported results.

Interventions

  • DRUG Bevacizumab
  • DRUG Temozolomide
  • DIETARY_SUPPLEMENT Vitamin C

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2013-07
Est. Completion 2022-01-31
Phase Phase 1

Sponsor

Vanderbilt-Ingram Cancer Center

189 total trials

What the Registry Record Tells You About NCT01891747

The ClinicalTrials.gov registry entry for NCT01891747 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 14 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt-Ingram Cancer Center, which has 189 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Bevacizumab is the first listed.

NCT01891747 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01891747 about?

NCT01891747 is a clinical study titled "A Phase I Study of High-dose L-methylfolate in Combination With Temozolomide and Bevacizumab in Recurrent High Grade Glioma". This is a Phase I/II non-randomized prospective study of high-dose L-methylfolate in combination with bevacizumab and temozolomide in patients with recurrent high-grade glioma. The primary objective of this phase II trial is to determine whether the addition of high-dose L-methylfolate to bevacizuma...

What is the current status of trial NCT01891747?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2013-07. Estimated completion is 2022-01-31.

What interventions are being tested in trial NCT01891747?

The interventions under investigation include: Bevacizumab (DRUG), Temozolomide (DRUG), Vitamin C (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT01891747?

This trial is sponsored by Vanderbilt-Ingram Cancer Center, which has 189 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.