drugset / Trial / NCT01107522

Safety and Tolerability of Carboxyamidotriazole Orotate (CTO) in Solid Tumors or With Temodar® in Glioblastoma or Other Recurrent Malignant Gliomas or in Combination With Temodar® and Radiation Therapy for Patients With Newly Diagnosed Glioblastoma and Malignant Gliomas

NCT01107522 ↗

Phase 1 Unknown 100 enrolled Tactical Therapeutics, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, tolerability, and the maximum tolerated dose/recommended phase II dose of carboxyamidotriazole orotate (CTO) as a single agent in patients with advanced or metastatic solid tumors; in combination with oral Temodar® in patients with glioblastoma or other recurrent malignant gliomas; or in combination with oral Temodar® and radiation therapy in patients with newly diagnosed glioblastoma or other malignant gliomas.

Timeline

Start
2010-05
Primary completion
2025-01
Completion
2026-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboxyamidotriazole Orotate Unknown 50 mg/m2 Oral
Subject Carboxyamidotriazole Orotate Unknown 219 mg/m2 Oral
Subject Carboxyamidotriazole Orotate Unknown 600 mg Oral
Subject Temozolomide Small molecule 150 mg/m2 Oral
Subject Temozolomide Small molecule 200 mg/m2 Oral

Indications