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Recruiting nowPhase 2Ages 18 Years and up

Riluzole For Preventing Cognitive Dysfunction in Ca Pts Receiving Chemo (REFOCUS): Pilot Trial

Sponsor: University of California, Irvine · NCT07447050 on ClinicalTrials.gov ↗

Conditions studied

Breast CancerSarcomaGastric (Stomach) CancerLung CancerHead and Neck CancerColorectal CancerOvarian CancerLiver CancerGenitourinary CancerGynecologic Cancer

What it tests

  • Riluzoledrug
  • Placeboother

Where it's running1 site

  • Chao Family Comprehensive Cancer Center, University of California Irvine

    Orange, California 92868

    Recruiting now
See the official eligibility language

Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.

Inclusion Criteria:

* Female and male patients diagnosed with cancer and planned to receive an anthracycline- or platinum- containing chemotherapy regimen.
* ≥18 years of age.
* Life expectancy \> 6 months
* Able to provide informed consent.
* Patients must agree to complete and be able to complete the questionnaires and computerized assessments used to measure functional outcomes. Note: Patients who have visual impairment or have degenerative conditions (e.g. Parkinsons's disease, etc.) can participate if they cannot complete computerized assessments, as long as they can still complete the questionnaires with assistance.

Exclusion Criteria:

* Presence of primary brain tumors or brain metastases.
* Receive a primary chemotherapy regimen that does not include anthracycline- or platinum- containing chemotherapy.
* Unwilling to undergo neuropsychological assessments necessary for the study.
* Patients who are breastfeeding, pregnant or are planning to get pregnant during the study period. POCBP must have a negative pregnancy test at screening if there is suspicion of pregnancy. Patients who are considered not to be of childbearing potential must have a history of being postmenopausal (with a minimum of 1 year without menses), tubal ligation, or hysterectomy.
* History of or suspected hypersensitivity to riluzole or to any of its excipients.
* Patients taking or planned to take medications/substances with potential drug-drug interactions: pixantrone, current smoker (defined as having smoked within the last month), abametapir, cannabis, capmatinib, lapatinib, methotrexate, and levoketoconazole.
* Hepatic impairment as indicated by: AST and/or ALT ≥ 3 X upper limit normal (ULN).
* Have serious pre-existing medical conditions that, in the judgment of the investigator, would preclude participation in this study.

Updated 2026-03-03 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.