Official Title
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Phase IIA Study of FSD201 (Ultramicronized PEA) + Standard of Care (SOC) Vs SOC in the Treatment of Hospitalized Patients With COVID-19
Brief Summary

This study will measure the effect of FSD201 (ultramicronized PEA) + SoC vs placebo + SoC on Day 28, on disease progression in the confirmed coronavirus disease 2019 (COVID-19) patient population.

Terminated
COVID-19

Drug: FSD201

Tablets for oral administration.
Other Name: ultramicronized palmitoylethanolamide (PEA)

Drug: Placebo

Placebo tablets matched to FSD201 for oral administration.

Other: Standard of Care for Covid-19

Standard of care for Covid-19 as determined by site PI

Eligibility Criteria

Inclusion Criteria:

- Must be willing and able to give informed consent to participate in the study

- Has admitted to a hospital and has a positive severe acute respiratory syndrome
coronavirus 2 (SARS-CoV-2) test by standard reverse transcription-polymerase chain
reaction (RT-PCR) assay or equivalent test

- Has the presence of any symptom(s) suggestive of moderate or severe systemic illness
with COVID-19 on Day 1 such as the presence of fever (greater than or equal to
(>=)38.0 degree Celsius [>=100.4 degree fahrenheit] by any route), "feeling hot,"
"feeling sweaty," headache, malaise, fatigue, muscle pain, diarrhea, nausea, vomiting,
cough, sore throat, or shortness of breath upon exertion and/or at rest, or
respiratory distress

- Has the presence of moderate to severe clinical signs indicative of moderate or severe
illness with COVID-19 on Day 1. A. Moderate: (1) Clinical signs suggestive of moderate
illness with COVID-19, such as respiratory rate >=20 breaths per minute, SpO2 >93% on
room air at sea level, heart rate >=90 beats per minute. (2) No clinical signs
indicative of severe or critical COVID-19. B. Severe: (1) Clinical signs suggestive of
severe systemic illness with COVID-19, such as respiratory rate >=30 breaths per
minute, heart rate >=125 beats per minute, SpO2 less than or equal to (<=) 93% on room
air at sea level or partial pressure of oxygen (PaO2)/fraction of inspired oxygen
(FiO2) less than (<)300, heart rate >=125 beats per minute. (2) No criteria met for
critical COVID-19

- Has either normal renal function or mild or moderate renal impairment: estimated
creatinine clearance >30 milliliters per minute (mL/min) on Day 1

- Able to swallow the study drug (tablets)

- Men whose sexual partners are women of childbearing potential (WOCBP) must agree to
comply with one of the following contraception requirements from the time of first
dose of study medication (Day 1) until at least 30 days after the last dose of study
medication: (a) Vasectomy with documentation of azoospermia. (b) Sexual abstinence.
(c) Male condom plus partner use of one of the contraceptive

- WOCBP must agree to comply with one of the following contraception requirements from
the time of first dose of study medication (Day 1) until at least 30 days after the
last dose of study medication: (a) Sexual abstinence (b) Use of one of the
contraceptive options (c) Vasectomy of male partner with documentation of azoospermia

Exclusion Criteria:

- The participant, in the opinion of the investigator, is not likely to survive for >=48
hours beyond Day 1

- Has a diagnosis of asymptomatic COVID-19, mild COVID-19, or critical COVID-19 on Day 1

- Has a documented current liver disease, or known hepatic or biliary abnormalities
(with the exception of asymptomatic gallstones) at screening or on Day 1

- Has a Child Pugh score >= C

- Has a documented medical history of infection with human immunodeficiency virus or
hepatitis A, B, or C at screening or on Day 1

- Has a documented active infection with tuberculosis at screening or on Day 1

- Has clinically significant ECG abnormalities at screening or on Day 1

- Requires dialysis or is on any renal replacement therapies at screening or on Day 1

- A female participant who is pregnant or planning to become pregnant during the study,
breastfeeding, or has a positive pregnancy test at screening

- Receiving alpha-blockers, combined alpha/beta blockers, antihistamines, or any drugs
that will affect the levels of cytokines released due to immune stress

- Has received any immunoglobulins within 6 months of screening or planned
administration of any immunoglobulins during the screening and/or treatment periods

- Has a known history of drug abuse within 6 months of study start that would interfere
with the participant's participation in the study

- Has a history of sensitivity to any of the study medications, or components thereof or
a history of drug or other allergy that, in the opinion of the investigator or medical
monitor, would contraindicate their participation

- Has participated in and/or plan to participate in another clinical study

- Will be transferred to another hospital which is not a study site within 72 hours

- Cannot read and speak either English or Spanish

Other protocol defined Inclusion/Exclusion criteria may apply

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United States
Locations

Miami, Florida
Miami, Florida, United States

Palms of Pasadena Hospital, Saint Petersburg, Florida
Saint Petersburg, Florida, United States

Theia Clinical Research, St. Petersburg, Florida
Saint Petersburg, Florida, United States

Idaho Falls, Idaho
Idaho Falls, Idaho, United States

Winfield, Illinois
Winfield, Illinois, United States

Butte, Montana
Butte, Montana, United States

Tulsa, Oklahoma
Tulsa, Oklahoma, United States

Kingsport, Tennessee
Kingsport, Tennessee, United States

Amarillo, Texas
Amarillo, Texas, United States

Mesquite, Texas
Mesquite, Texas, United States

FSD Pharma, Inc.
NCT Number
Keywords
SARS-CoV-2
MeSH Terms
COVID-19
Palmidrol