RecruitingPhase 1Phase 2NCT07599371

A Prospective, Single-arm Clinical Study on the Safety and Efficacy of Ivoximab Combined With Temozolomide in the Treatment of Relapsed/Refractory Glioma


Sponsor

The First Affiliated Hospital of Zhengzhou University

Enrollment

29 participants

Start Date

Oct 10, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study is a prospective, single-arm clinical trial aimed at evaluating the safety and efficacy of ivoximab combined with temozolomide in the treatment of relapsed/refractory glioma. The study plans to enroll 29 patients with relapsed/refractory glioma. After signing informed consent and meeting the inclusion/exclusion criteria through screening, patients will receive treatment with ivoximab combined with temozolomide. Efficacy evaluation will be conducted every two treatment cycles using the Response Assessment in Neuro-Oncology (RANO 2.0) criteria, and treatment will continue until disease progression or intolerance to the combined regimen.


Eligibility

Min Age: 18 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Ivoximab 20 mg/kg, ivgtt, Q4W and a drug called Temozolomide (TMZ) for people with relapsed/refractory glioma. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 85 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIvoximab 20 mg/kg, ivgtt, Q4W

We have not found any treatment recorded as this combination

DRUGTemozolomide (TMZ)

Temozolomide 150 mg/m², D1-D5, P.O., Q4W


Locations(1)

The first affiliated hospital of Zhengzhou university

Zhengzhou, Henan, China

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NCT07599371