COVID-19 First In Human Study to Evaluate Safety, Tolerability, and Pharmacokinetics of EIDD-2801 in Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

130

Participants

Timeline

Start Date

April 10, 2020

Primary Completion Date

August 11, 2020

Study Completion Date

August 11, 2020

Conditions
Coronavirus
Interventions
DRUG

EIDD-2801

"Part 1:~Participants will be randomized to receive a single oral dose of EIDD-2801 or Placebo.~Part 2:~Two single oral doses of EIDD-2801 will be administered to participants, in an open-label manner.~Part 3:~Participants will be randomized to receive twice daily dosing either EIDD-2801 or Placebo."

DRUG

Placebo

"Part 1:~Participants will be randomized to receive a single oral dose of EIDD-2801 or Placebo.~Part 3:~Participants will be randomized to receive twice daily dosing either EIDD-2801 or Placebo."

Trial Locations (1)

Unknown

Covance Leeds Clinical Research Unit, Leeds

All Listed Sponsors
lead

Ridgeback Biotherapeutics, LP

INDUSTRY

NCT04392219 - COVID-19 First In Human Study to Evaluate Safety, Tolerability, and Pharmacokinetics of EIDD-2801 in Healthy Volunteers | Biotech Hunter | Biotech Hunter