Evaluate the Safety, Tolerability and PK of HF1K16 in Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

March 20, 2021

Primary Completion Date

July 30, 2021

Study Completion Date

August 4, 2021

Conditions
Healthy
Interventions
DRUG

HF1K16

HF1K16 for Injection doses will be calculated based on subject weight measured at admission, and diluted in sterile saline (0.9% sodium chloride). Doses will be administered using an IV infusion pump over a period of approximately 60 minutes at 2.5 mL/min.

DRUG

Placebo

Placebo will be sterile saline (0.9% sodium chloride) which will be administered using an IV infusion pump over a period of approximately 60 minutes at 2.5 mL/min.

Trial Locations (1)

07094

Frontage Clinical Services, Inc., Secaucus

All Listed Sponsors
lead

HighField Biopharmaceuticals Corporation

INDUSTRY