Repurposing Riluzole for Cancer-Related Cognitive Impairment: A Pilot Trial

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of California, Irvine

About this trial

This is a phase 2a, randomized, double-blinded, placebo-controlled pilot clinical trial determining the impact of riluzole therapy on circulating brain derived neuropathic factor (BDNF) levels of cancer survivors with cancer related cognitive impairment.

Eligibility criteria

Qualifiers

Breast cancer exposed to treatment including chemotherapy, radiotherapy, surgery and/or other breast cancer interventions

Non-breast cancer patients exposed to anthracyclines- or platinum-containing chemotherapy within the past 3 years

Non-breast cancer patients exposed to other anticancer therapies within the past 3 years

Washout from investigational interventions is up to the discretion of the Investigator. Concurrent participation in another intervention is allowable if judged by the Principal Investigator that this would not be scientifically or medically incompatible with this study.

Disqualifiers

Presence of brain metastasis

Unwilling to undergo neuropsychological assessments necessary for the study.

Women who are breastfeeding, pregnant or are planning to get pregnant during the study period. Women of child-bearing potential (WOCBP) must have a negative pregnancy test at screening if there is suspicion of pregnancy.

History of suspected hypersensitivity to riluzole or to any of its excipients.

Trial design

Treatments tested in this trial

  • Riluzole
  • Placebo

Treatment groups

51 Participants
are divided into 2 treatment groups