Summary

Eligibility
for people ages 18-69 (full criteria)
Location
at UCSF
Dates
study started
study ends around

Description

Summary

Long COVID is a condition where debilitating symptoms can persist for months after a COVID-19 infection. This study aims to evaluate the effects of NE3107 on several neurological symptoms reported in people with Long COVID including difficulty concentrating or remembering things ("brain fog") and fatigue.

Researchers will compare NE3107 to a placebo (a look-alike substance that contains no drug) to see if NE3107 works to treat neurocognitive and fatigue symptoms of long COVID.

Participants will:

  • Take NE3107 or a placebo twice daily for 84 days
  • Visit the clinic 5 times for checkups and tests and have a follow up phone call

Official Title

A Double-blind, Randomized Study to Evaluate the Efficacy and Safety of Bezisterim (NE3107) in Adults With Long COVID

Keywords

Long COVID, COVID-19, Neurocognition, Fatigue, Post-exertional malaise, Sleep, SARS-CoV-2, Brain fog, Post-Acute COVID-19 Syndrome, Mental Fatigue

Eligibility

You can join if…

Open to people ages 18-69

  • 18 years to 69 years of age
  • Long COVID with neurological symptoms as defined below:
    1. Current symptoms of at least fatigue and neurocognitive impairment that began or worsened after an index SARS-CoV-2 infection that occurred at least 3 months prior to screening. Index SARS-CoV-2 infection is defined as either: 1) an episode of COVID-19 with a positive nucleic acid or antigen test during acute illness, as documented in the medical record, or 2) a documented clinical diagnosis of COVID-19, which can be based on a patient-reported positive test for COVID-19. Note that a documented diagnosis of Long COVID is not required for inclusion.
    2. Symptoms cannot be explained by any concomitant condition or diagnosis, in the opinion of the investigator.
    3. Symptom duration for at least 3 months. diagnosed with Long COVID with symptoms of fatigue and brain fog for at least 3 months
  • Agree to maintain any other regular medications at current doses for the duration of the trial (except for essential need of new medication or dose change, as prescribed by a physician)
  • Agree to use birth control measures
  • Provide voluntary consent
  • Willing to allow blood collection
  • Pass all screening tests and procedures

You CAN'T join if...

  • Has received a COVID-19 vaccination within 14 days
  • Previous admission to the intensive care unit for COVID-19
  • Medical history of major mental or physical illness prior to COVID-19 infection

Locations

  • UCSF accepting new patients
    San Francisco California 94110 United States
  • Stanford University accepting new patients
    Palo Alto California 94304 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
BioVie Inc.
Links
ADDRESSLC Study website
ID
NCT06847191
Phase
Phase 2 COVID-19 Research Study
Study Type
Interventional
Participants
Expecting 208 study participants
Last Updated