24 Participants NeededMy employer runs this trial

Riluzole for Cognitive Dysfunction in Cancer

CF
Overseen ByChao Family Comprehensive Cancer Center University of California, Irvine
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This is a phase II single-arm, Phase 2a, randomized, double-blinded, placebo-controlled pilot clinical trial determining efficacy of riluzole in preventing cognitive dysfunction in subjects with cancer, who are receiving chemotherapy.

Who Is on the Research Team?

AC

Alexandre Chan, PharmD, MPH

Principal Investigator

Chao Family Comprehensive Cancer Center

Are You a Good Fit for This Trial?

Inclusion Criteria

* 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.
I have cancer and will receive anthracycline or platinum chemotherapy.
I am 18 years old or older.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either riluzole or placebo twice daily for up to 6 months

6 months
Regular visits for safety monitoring and cognitive assessments

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Riluzole

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: RiluzoleExperimental Treatment1 Intervention
Group II: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, Irvine

Lead Sponsor

Trials
580
Recruited
4,943,000+