drugset / Trial / NCT04091503

Evaluate the Safety and Effectiveness of Intranasal Administration of Temozolomide in Patients With Glioblastoma

NCT04091503

Phase 1 Completed 30 enrolled Center Trials & Treatment Europe
RandomizedSingle-groupSingle-blindTreatment

Summary

The purpose of this pilot study is to determine the safety, tolerability, and the maximum tolerated dose intranasal administration of temozolomide (TMZ) as a single agent in Treatment on the patients with GBM. Intranasal administration is a new method of treating brain tumours for the direct administration of drugs, inhibitors or viruses, with minimal involvement of the BBB. The investigators know the orally prescribed standard chemotherapy temozolomide (TMZ) is widely used to treat glioma tumours. Received evidence of safety and efficacy in a full cycle of preclinical trials (on GLP Standart) and tests of calculated doses of intranasal administration of TMZ in healthy volunteers. Intranasal administration of temozolomide is considered as GBM therapy, which provides direct access to a therapeutic dose of the drug into the brain (to the neoplastic process) with low toxicity

Timeline

Start
2019-12-20
Primary completion
2022-09-21
Completion
2022-10-28

Drugs

EvaluationDrugModalityDoseRoute
Comparator Temozolomide Small molecule 75 mg/m2 Intranasal
Comparator Temozolomide Small molecule 150 mg/m2 Intranasal
Comparator Temozolomide Small molecule 200 mg/m2 Intranasal