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Trials / Enrolling By Invitation

Enrolling By InvitationNCT05787418

HH-120 Nasal Spray for Post-exposure Prevention of SARS-CoV-2

A Phase III, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of HH-120 Nasal Spray for Post-exposure Prophylaxis of SARS-CoV-2

Status
Enrolling By Invitation
Phase
Phase 3
Study type
Interventional
Enrollment
1,200 (estimated)
Sponsor
Huahui Health · Industry
Sex
All
Age
12 Years – 85 Years
Healthy volunteers
Not accepted

Summary

This study will assess the efficacy of HH-120 nasal spray in participants for the post-exposure prevention of SARS-CoV-2.

Detailed description

During this study, participants will receive HH-120 nasal spray treatment for 7 consecutive days, the efficacy and safety of HH-120 nasal spray will be assessed throughout the study period mainly based on the incidence of symptomatic SARS-CoV-2 infection and adverse events, respectively.

Conditions

Interventions

TypeNameDescription
DRUGHH-120 Nasal SprayHH-120 nasal spray 8 times per day for 7 consecutive days
DRUGPlaceboPlacebo 8 times per day for 7 consecutive days

Timeline

Start date
2023-03-31
Primary completion
2025-12-31
Completion
2026-04-01
First posted
2023-03-28
Last updated
2024-10-10

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05787418. Inclusion in this directory is not an endorsement.