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NOT YET RECRUITING
NCT07707973
PHASE2

Nimotuzumab Combined With the Stupp Regimen for Postoperative Residual Glioblastoma

Sponsor: Tianjin First Central Hospital

View on ClinicalTrials.gov

Summary

This is a prospective, single-arm study. The study population consists of adult patients with a confirmed diagnosis of EGFR-positive high-grade glioma who have radiographic residual tumor following surgical resection. Participants will receive nimotuzumab in combination with the standard Stupp regimen after glioma surgery.

Official title: A Single-arm, Phase II Study of Nimotuzumab Combined With the Stupp Regimen for Postoperative Residual Glioblastoma

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2026-07-03

Completion Date

2029-06-03

Last Updated

2026-07-16

Healthy Volunteers

No

Interventions

DRUG

nimotuzumab

Nimotuzumab 200 mg will be administered via intravenous infusion once weekly for 6 weeks, followed by 200 mg via intravenous infusion once every 4 weeks for a total of 6 doses.

DRUG

Temozolomide

Temozolomide will be administered orally at a dose of 150-200 mg/m²/day for 5 consecutive days. Each cycle lasts 28 days, for a total of 6 cycles.

RADIATION

Radiotherapy

PTV:60Gy/2Gy/30f,6weeks