Recruiting

Temozolomide vs. Evening

Sponsor:

Ottawa Hospital Research Institute

Code:

NCT06850766

Conditions

IDH-Wildtype Glioblastoma

Glioblastoma (GBM)

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Morning administration of TMZ

Evening administration of TMZ

Study Details

Brief summary:

The body's biological functions follow a circadian rhythm, meaning that individual biological functions in the body change over a 24-hour cycle. There is evidence suggesting that the body and cancer cells may react differently to anti-cancer treatment based on the time of day they are exposed. In fact, researchers have already found that giving anti-cancer treatments at a particular time of the day works better in rectal and ovarian cancer. Temozolomide (TMZ) is a chemotherapy pill/capsule commonly given to patients with newly diagnosed glioblastoma after brain surgery and radiation treatment. However, there is no current standard for what time of day TMZ should be taken for the treatment of glioblastoma.

In the current study, participants are randomly placed in one of two groups: a morning group and an evening group. Based on this group placement, participants are instructed to either take their TMZ in the morning or in the evening and record the date and time they take their TMZ in a pill diary. Participants will wear a wrist actigraphy device for the first cycle of TMZ. The primary goal of the study is to understand if taking TMZ at a prescribed time of day (morning/evening) is feasible in adults with glioblastoma. This is a pilot trial, and the investigators hypothesize that it will be feasible for glioblastoma patients to take TMZ at the prescribed time of day. The secondary goals of this study are to evaluate participant recruitment, safety, health-related quality of life, biological timing of TMZ delivery, and changes in condition over time. This pilot study will help investigators plan for a larger, pragmatic randomized clinical trial in the future.

Conditions

IDH-Wildtype Glioblastoma

Glioblastoma (GBM)

Study ID

NCT06850766

Start date

May 8, 2025

Status verified date

Jul, 2026

Completion date

Nov, 2031

Anticipated

Primary completion date

May, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 18 years of age or older
  • Newly diagnosed IDH-wildtype glioblastoma
  • Completed maximal safe brain tumor resection
  • Completed post-operative brain RT
  • Plan to proceed with up to 6 cycles of adjuvant TMZ within 8 weeks of completing post-operative RT
  • Able and willing to provide oral informed consent

Exclusion Criteria:

  • Unable or unwilling to complete study questionnaires
  • Metastatic or incurable cancer other than IDH-wild type glioblastoma

Study Design

Enrollment

50 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Morning administration of TMZ

Participants were instructed to take the prescribed daily dose of temozolomide (TMZ) in the morning.

active comparator: Evening administration of TMZ

Participants were instructed to take the prescribed daily dose of temozolomide (TMZ) in the evening.

Interventions

Morning administration of TMZ

Administration of TMZ within 2 hours of waking

Evening administration of TMZ

Administration of TMZ within 2 hours of bedtime

Primary outcome measure

  • Feasibility: adherence to TMZ dose timing protocol [ Time Frame: Patients complete daily pill diaries on days 1-5 of a 28-day cycle for up to 6 cycles. It is expected that the first cycle will begin within 8 weeks of the last fraction (dose) of radiation. Adherence is calculated at Week 48. ]

Central Contacts and Locations

Central contacts

Locations

London Health Sciences Centre

Recruiting

London, Ontario, Canada, N6A 5W9

Contacts

Seth Climans, MD

519-685-8600

Principal Investigator:

Seth Climans, MD

The Ottawa Hospital Cancer Centre

Recruiting

Ottawa, Ontario, Canada, K1H 8L6

Contacts

Principal Investigator:

Terry Ng, MD

More Information

Sponsor

Ottawa Hospital Research Institute

Last update posted

Jul 16, 2026

Last verified

Jul, 2026

Keywords

  • temozolomide
  • chronotherapy
  • dose timing
  • cancer
  • oncology
  • glioblastoma
  • chemotherapy

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Ottawa Hospital Research Institute on 2026-07-16.