Solriamfetol in Improving Sleep in Patients With Grade II-IV Glioma

Exclusion Criteria

• •Patients who are anticipated to undergo adjuvant chemotherapy are eligible as long as there is no evidence of tumor progression by clinical exam and/or imaging within 21 days of enrollment (see 4.1.2). This determination should be made by clinical documentation and if there is question discussed with the Study Chair. Adjuvant chemotherapy is not an exclusion.
• •Age \> 18 years
• •Karnofsky performance status ≥ 60%
• •Life expectancy of greater than 4 months
• •Patients must have normal organ and marrow function as defined below:
• •leukocytes \>3,000/mcL absolute neutrophil count \>1,500/mcL platelets \>100,000/mcL total bilirubin 1.5 X institutional upper limits of normal AST(SGOT)/ALT(SGPT) \<2.5 X institutional upper limit of normal creatinine within normal institutional limits OR creatinine clearance \>50 mL/min/1.73 m2 for patients with creatinine levels above institutional normal.
• •The effects of solriamfetol on the developing human fetus are unknown. For this reason women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately
• •Ability to understand and the willingness to sign an IRB-approved informed consent document (either directly or via a legally authorized representative)
• •Receiving active radiation therapy (including patients who are within 28 days of completing radiation therapy)
• •Anticipated to undergo radiation therapy or require neurosurgical intervention during the period of active treatment(i.e. within the next 4 months)
• •Contraindication to solriamfetol based on drug-drug interactions or concurrent systemic illness that precludes drug treatment
• •Patients who have not recovered to \< CTCAE grade 2 toxicities related to prior or current therapy are ineligible.
• •Exception for laboratory-based or other adverse event that is stable and not anticipated to interfere with study related treatment must be reviewed and approved by the study chair
• •Customary bedtime later than midnight
• •Known and/or documented history of obstructive sleep apnea (OSA)
• •Uncontrolled behavioral or psychiatric disorder (including suicidal ideation)
• •Current excessive caffeine use (\> 600 mg/day or \> 6 cups of coffee/day)
• •Current or prior history of alcohol or drug abuse within the last 2 years as assessed by the treating clinician
• •Nicotine dependence that is currently interfering with sleep based on assessment by the treating clinician
• •Concurrent use of selective serotonin or norepinephrine reuptake inhibitors (e.g. selective serotonin reuptake inhibitor \[SSRI\], serotonin and norepinephrine reuptake inhibitors \[SNRI\]) within 14 days of study enrollment
• •Patients who are currently taking these agents may be tapered at the direction of the treating physician prior to study enrollment
• •Patients taking other medications such as narcotics, benzodiazepines, antipsychotics, antiepileptics, corticosteroids, or over-the-counter sleep aids can be enrolled. It is recommended that the doses of these medications remain the same throughout the portion of active study treatment unless there is a medical indication for dose adjustment which will be determined by the treating physician
• •History of allergic reactions attributed to compounds of similar chemical or biologic composition to solriamfetol
• •Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
• •Pregnant women are excluded from this study because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with solriamfetol, breastfeeding should be discontinued if the mother is treated with solriamfetol