An Investigator-initiated, Randomized, Single-Blind, Placebo-Controlled Trial to Evaluate the Efficacy of SARS-Cov-2 Post Exposure Prophylaxis and Safety of HH-120 nasal spray
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
281
HH-120 nasal spray 5 times daily for 3 consecutive days
HH-120 nasal spray 8 times daily for 3 consecutive days
Placebo nasal spray 5 times daily for 3 consecutive days
Beijing Ditan Hospital,Capital Medical University
Beijing, Beijing Municipality, China
Proportion of subjects who have a RT-qPCR confirmed SARS-CoV-2 infection.
Time frame: Day 1 to Day 10
Proportion of subjects who have a symptomatic RT-qPCR confirmed SARS-CoV-2 infection.
Time frame: Day 1 to Day 10
Proportion of subjects who have an asymptomatic RT-qPCR confirmed SARS-CoV-2 infection.
Time frame: Day 1 to Day 10
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Placebo nasal spray 8 times daily for 3 consecutive days