Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06747728

Bevacizumab Neoadjuvant Therapy for New High-grade Gliomas in the Brain

Led by The First Affiliated Hospital of Zhengzhou University · Updated on 2024-12-24

20

Participants Needed

1

Research Sites

117 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on patients with new-onset high-grade gliomas, a type of brain tumor known as glioblastoma (GBM) that grows diffusely and invades surrounding brain tissue. The tumor's aggressive nature and its tendency to recur shortly after surgery contribute to poor outcomes. GBM is characterized by abnormal blood vessel growth, and blocking this process is a key therapeutic approach. The study aims to evaluate the safety and effectiveness of bevacizumab, a drug that inhibits blood vessel growth in tumors, when given before surgery as an additional treatment. Participants receive bevacizumab administered intravenously at a dose of 5 mg/kg on days 1 and 15 before surgery. This treatment is intended to reduce tumor blood vessel formation and limit tumor growth. The study does not mention other treatment groups or comparators but focuses on assessing bevacizumab as a neoadjuvant therapy to potentially improve surgical outcomes. During the study, researchers will monitor participants for approximately two years to measure the objective response rate, which reflects how well the tumor responds to treatment. Assessments may include imaging and clinical evaluations to track tumor status and patient health. Safety and tolerability of bevacizumab will also be closely observed throughout the treatment and follow-up periods, ensuring comprehensive monitoring of outcomes and adverse events.

CONDITIONS

Official Title

Bevacizumab Neoadjuvant Therapy for New High-grade Gliomas in the Brain

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 2 18 years or older
  • Male or female
  • Imaging diagnosis of high-grade glioma
  • Karnofsky Performance Status (KPS) score of 60 or higher
Not Eligible

You will not qualify if you...

  • Previous treatment with anti-angiogenic targeted drugs
  • Serious cardiac, pulmonary, hepatic, or renal disease
  • History of arterial or venous blood clots within 6 months before screening
  • Infectious diseases such as tuberculosis or viral hepatitis
  • Uncontrolled high blood pressure, bleeding disorders, or unhealed wounds or fractures
  • History of psychotropic substance abuse that cannot be stopped or mental disorders
  • Abnormal blood clotting with bleeding tendency
  • Conditions that make participation unsuitable, such as pregnancy or breastfeeding

AI-Screening

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Trial Site Locations

Total: 1 location

1

The First Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, China

Actively Recruiting

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Research Team

J

Junkuan Wang, M.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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