Overview
A Study to Assess the Efficacy of HH-120 Nasal Spray for Prevention of SARS-CoV-2 Infection in Adult Close Contacts of Individuals Infected With SARS-CoV-2
Status:
Completed
Completed
Trial end date:
2022-12-06
2022-12-06
Target enrollment:
0
0
Participant gender:
All
All
Summary
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 sprayPhase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Beijing Ditan Hospital
Criteria
Inclusion Criteria:- Participants aged 18 to 65 years.
- Participants who have close contact with a SARS-CoV-2 infected individual (index case)
are required to be randomized within 72 hours upon close contact.
- Willing and able to provide written informed consent, or with a legal representative
who can provide informed consent.
Exclusion Criteria:
- Have a history of severe allergy or hyper-sensitivity to inhaled allergen.
- Pregnant or breastfeeding women.
- Have participated, within the last 180 days prior to the screening, in a clinical
study involving an investigational intervention of SARS-CoV-2 neutralizing antibody.
- Have other conditions not suitable for the study per investigator's discretion.