Amantadine Therapy for Cognitive Impairment in Long COVID

Inclusion Criteria:

1. 18 years of age and above at the signing of informed consent

2. Had a positive laboratory or home test for COVID19 within one year prior to signingof informed consent, with subsequent symptoms meeting criteria for PASC.

3. Subjective Cognitive impairment associated with PASC

4. Cognitive symptoms will be formally assessed at a pre-enrollment visit using thePROMIS Cognitive Function Questionnaire (CGQ) and the PROMIS Cognitive Abilitiessubset (CAS), which are validated patient-reported measures of subjective cognitivefunctioning. Potential participants must have a cumulative score less than 60 (indicating at least mild subjective cognitive dysfunction) to be eligible.

5. Is willing and able to comply with study visits and study-relatedprocedures/assessments.

6. Is able to provide informed consent to participate in the study 5.

7. Is not currently taking a medication with adverse interactions with amantadine. (Table 2)

8. If the participant is of child bearing potential, , is not pregnant at enrollmentbased on negative urine pregnancy test.

9. If the participant is of child-bearing potential, is consistently using one or moreforms of prescribed birth control, such as an oral contraceptive, intrauterinedevice or a long-acting reversible contraceptive.

10. Is not breastfeeding.

11. Is willing to abstain from alcohol use for the duration of the study.

12. Endorses self-reported cognitive impairment on the PROMIS CF[40].

13. Does not have any other contraindications to amantadine use as noted in section 6below or as identified by the study clinician investigators.

Exclusion Criteria:

1. At risk for complications of study drug with conditions such as:

• Lifetime history of compulsive or impulsive behavior: Compulsive gambling,hypersexuality, binge eating; suicidality.

• Underweight, malnourished at time of enrollment.

• History of restrictive eating disorder within 3 months prior to consent.

• Lifetime history of heart failure or diagnosed cardiac arrhythmia.

• Untreated angle closure glaucoma at time of enrollment.

• Lifetime history of psychosis or psychotic disorder.

• Lifetime history of seizure disorder.

• Known allergy to amantadine.

• History of binge drinking, heavy alcohol use, or alcohol use disorder asdefined by the National Institute on Alcohol Abuse and Alcoholism (NIAAA)[54]and the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5)[55].

• Use of kava-kava within 3 months prior to consent.

• Breastfeeding at screening or expected to be breastfeeding during study period.

• Pregnant at time of screening or expecting to become pregnant during the studyperiod.

2. Is taking a medication that adversely interacts with amantadine (see Table 2)

3. Has any physical examination findings, and/or history of any illness, concomitantmedications or recent live vaccines that, in the opinion of the study investigator,might confound the results of the study or pose an additional risk to the subject bytheir participation in the study.

4. Prior diagnosis of dementia, neurodegenerative disorder, multiple sclerosis or otherautoimmune neurologic disorder, or cognitive impairment.

5. Enrolled in any other research study involving intervention for PASC.

6. If the individual is of child-bearing potential, is not consistently using one ormore forms of prescribed birth control.

7. Is not willing to abstain from alcohol for the duration of the study.

8. Is not willing and able to adhere to study visits and study-relatedprocedures/assessments.

9. Is not able to provide informed consent to participate in the study.