Ultramicronized Palmitoylethanolamide (PEA) Treatment in Hospitalized Participants With COVID-19

PHASE2TerminatedINTERVENTIONAL
Enrollment

53

Participants

Timeline

Start Date

December 14, 2020

Primary Completion Date

August 24, 2021

Study Completion Date

August 24, 2021

Conditions
COVID-19
Interventions
DRUG

FSD201

Tablets for oral administration.

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

Trial Locations (10)

33155

Miami, Florida, Miami

33707

Palms of Pasadena Hospital, Saint Petersburg, Florida, St. Petersburg

Theia Clinical Research, St. Petersburg, Florida, St. Petersburg

37660

Kingsport, Tennessee, Kingsport

59701

Butte, Montana, Butte

60190

Winfield, Illinois, Winfield

74104

Tulsa, Oklahoma, Tulsa

75149

Mesquite, Texas, Mesquite

79109

Amarillo, Texas, Amarillo

83404

Idaho Falls, Idaho, Idaho Falls

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Quantum Biopharma

INDUSTRY

NCT04619706 - Ultramicronized Palmitoylethanolamide (PEA) Treatment in Hospitalized Participants With COVID-19 | Biotech Hunter | Biotech Hunter