CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 279 enrolled
Drug / intervention
concurrent RAD001 10 mg/day +6 moredrug
Likely dose
concurrent RAD001 10 mg/dayfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01062399
NCT01062399Phase 2Completed

Phase I/II Trial of Concurrent RAD001 (Everolimus) With Temozolomide/Radiation Followed by Adjuvant RAD001/Temozolomide in Newly Diagnosed Glioblastoma

Radiation Therapy Oncology Group·interventional·Posted Feb 4, 2010·Updated Jun 9, 2022

In Brief

A Phase 2 clinical trial evaluating concurrent RAD001 10 mg/day, concurrent temozolomide, and 5 other interventions for Brain and Central Nervous System Tumors. Completed, enrolled 279 participants across 36 sites in 3 countries.

Detailed Summary

RATIONALE: Everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high energy x-rays to kill tumor cells. Giving everolimus together with temozolomide and radiation therapy may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of everolimus when given together with temozolomide and radiation therapy and to see how well it works in treating patients with newly diagnosed glioblastoma multiforme.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Israel, United States

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 4, 2010
Enrollment StartDec 1, 2010
Primary CompletionJun 1, 2016
Study CompletionMay 20, 2022
TodayJul 2, 2026
Enrollment to primary: 5.5 yearsPosted 16.4 years ago

Interventions

concurrent RAD001 10 mg/daydrug

During radiation: RAD001 10 mg orally daily during radiation therapy; one hour prior to radiation and in the morning on weekends on days 1-42.

concurrent temozolomidedrug

During radiation: temozolomide 75 mg/m2/day orally daily during radiation therapy; one hour prior to radiation and in the morning on weekends on days 1-42. Dose rounded to the nearest 5 mg.

Radiation therapyradiation

Intensity Modulated RT (IMRT) allowed. For both IMRT and 3D conformal radiotherapy (3D-CRT) plans, one treatment of 2 Gy given daily 5 days per week for a total of 60 Gy over 6 weeks.

concurrent RAD001 2.5 mg/daydrug

During radiation: RAD001 2.5 mg orally daily during radiation therapy; one hour prior to radiation and in the morning on weekends on days 1-42.

concurrent RAD001 5 mg/daydrug

During radiation: RAD001 5 mg orally daily during radiation therapy; one hour prior to radiation and in the morning on weekends on days 1-42.

post-radiation RAD001 10 mg/daydrug

Post-radiation: RAD001 10 mg orally daily on days 1-28 of each cycle, for up to 12 cycles, starting 28 days after the completion of radiation therapy (Cycle = 28 days).

post-radiation temozolomidedrug

Post-radiation: temozolomide 150 mg/m2/day - 200 mg/m2/day orally daily on days 1-5 of each cycle, starting 28 days after the completion of radiation therapy for up to 12 cycles (Cycle = 28 days)