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NCT01106872 · ClinicalTrials.gov registry record · Phase 1

Bevacizumab, Chemotherapy and Valproic Acid in Advanced Sarcomas

A Phase 1 study of Sarcoma and Soft Tissue Sarcoma, sponsored by Mohammed M Milhem.

Completed
Registry status
Phase 1
Development phase
47
Enrollment target
1
Study location

NCT01106872 is a Phase 1 study of Sarcoma and Soft Tissue Sarcoma that has completed, run by Mohammed M Milhem. The registered enrollment target is 47 participants, below the 921-participant average among 122 other Sarcoma trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01106872, a Phase 1 study of Sarcoma and Soft Tissue Sarcoma, has completed, sponsored by Mohammed M Milhem.

COMPLETED
Registry status
Phase 1
Development phase
47 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to test the combination of the chemotherapy drugs Gemcitabine, bevacizumab, and docetaxel with valproic acid to treat patients with metastatic sarcoma. Valproic acid is used by people who have seizures to prevent seizures from happening; however, its use in cancer is investigational. This study will help define the proper dosing of this valproic acid. We will assess the safety of valproic acid with the combination of the above chemotherapy drugs and check for possible side effects. Valproic acid may improve the function of the chemotherapy drugs against the cancer.

Interventions

  • DRUG Bevacizumab, Gemcitabine, Docetaxel and Valproic Acid

Study Locations (1)

Iowa

  • University of Iowa Hospitals and Clinics - Iowa City

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2010-09
Est. Completion 2017-08-22
Phase Phase 1

Sponsor

Mohammed M Milhem

2 total trials

What the Registry Record Tells You About NCT01106872

The ClinicalTrials.gov registry entry for NCT01106872 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 47 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 921-participant average among 122 other Sarcoma trials with a reported enrollment target (95% lower). The listed sponsor is Mohammed M Milhem, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Sarcoma appearing as the primary indexed condition, and to 1 intervention - of which Bevacizumab, Gemcitabine, Docetaxel and Valproic Acid is the first listed.

NCT01106872 reports 1 study location spanning 1 distinct geographic area - top geographies include Iowa.

Frequently Asked Questions

What is clinical trial NCT01106872 about?

NCT01106872 is a clinical study titled "Bevacizumab, Chemotherapy and Valproic Acid in Advanced Sarcomas". The purpose of this study is to test the combination of the chemotherapy drugs Gemcitabine, bevacizumab, and docetaxel with valproic acid to treat patients with metastatic sarcoma. Valproic acid is used by people who have seizures to prevent seizures from happening; however, its use in cancer is inv...

What is the current status of trial NCT01106872?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2010-09. Estimated completion is 2017-08-22.

What conditions does trial NCT01106872 study?

This clinical trial studies the following conditions: Sarcoma, Soft Tissue Sarcoma, Metastatic Sarcoma, Locally Advanced Sarcoma, Unresectable Sarcoma.

What interventions are being tested in trial NCT01106872?

The interventions under investigation include: Bevacizumab, Gemcitabine, Docetaxel and Valproic Acid (DRUG).

Who is sponsoring clinical trial NCT01106872?

This trial is sponsored by Mohammed M Milhem, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01106872 being conducted?

This trial has 1 study location across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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