16
Participants
Start Date
March 20, 2021
Primary Completion Date
July 30, 2021
Study Completion Date
August 4, 2021
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.
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.
Frontage Clinical Services, Inc., Secaucus
Lead Sponsor
HighField Biopharmaceuticals Corporation
INDUSTRY