VNRX-5024 Safety and PK in Healthy Adult Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

July 27, 2020

Primary Completion Date

December 31, 2020

Study Completion Date

December 31, 2020

Conditions
Healthy Subjects
Interventions
DRUG

VNRX-5024

"Part 1: one dose~Part 2:~Cohort 1: 10 doses (once a day for 10 days) Cohort 2: 19 doses (once every 12 hours \[q12h\] dosing for 9 days with a single morning dose on Day 10) Cohort 3: 28 doses (once every 8 hours \[q8h\] dosing for 9 days with a single morning dose on Day 10)"

DRUG

Placebo for VNRX-5024

"Part 1: one dose~Part 2:~Cohort 1: 10 doses (once a day for 10 days) Cohort 2: 19 doses (once every 12 hours \[q12h\] dosing for 9 days with a single morning dose on Day 10) Cohort 3: 28 doses (once every 8 hours \[q8h\] dosing for 9 days with a single morning dose on Day 10)"

Trial Locations (1)

Unknown

PRA Health Sciences - Early Development Services, Groningen

All Listed Sponsors
collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

lead

Venatorx Pharmaceuticals, Inc.

INDUSTRY

NCT04314206 - VNRX-5024 Safety and PK in Healthy Adult Volunteers | Biotech Hunter | Biotech Hunter