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

NCT05787418 · Status: ENROLLING_BY_INVITATION · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1200

Last updated 2024-10-10

No results posted yet for this study

Summary

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

Conditions

Interventions

DRUG

HH-120 Nasal Spray

HH-120 nasal spray 8 times per day for 7 consecutive days

DRUG

Placebo

Placebo 8 times per day for 7 consecutive days

Sponsors & Collaborators

  • Huahui Health

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-31
Primary Completion
2025-12-31
Completion
2026-04-01

Countries

  • China

Study Locations

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Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05787418 on ClinicalTrials.gov