Trials / Unknown
UnknownNCT05200741
To Evaluate Safety & Immunogenicity of DelNS1-2019-nCoV-RBD-OPT1 for COVID-19 in Healthy Adults Received 2 Doses of BNT162b2
A Randomized, Double-blinded, Placebo-controlled Study to Evaluate the Safety and Immunogenicity of DelNS1-2019-nCoV-RBD-OPT1 as Booster Vaccine for COVID-19 in Healthy Adults Who Have Received 2 Doses of BNT162b2
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 150 (estimated)
- Sponsor
- The University of Hong Kong · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
To evaluate the safety and immunogenicity of DelNS1-2019-nCoV-RBD-OPT1 as booster vaccine for COVID-19 in healthy adults who have received 2 doses of BNT162b2
Detailed description
This is a randomized, double-blinded, placebo-controlled study to evaluate the safety and immunogenicity of DelNS1-2019-nCoV-RBD-OPT1 as booster vaccine for COVID-19 in healthy adults who have received 2 doses of BNT162b2. Each subject will receive 2 vaccinations or matching placebo 3 weeks apart.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | DelNS1-2019-nCoV-RBD-OPT1 | Influenza Virus Vector COVID-19 Vaccine for Intranasal Spray |
| BIOLOGICAL | Matching placebo | Solution for Intranasal Spray |
Timeline
- Start date
- 2022-02-08
- Primary completion
- 2024-02-01
- Completion
- 2024-02-01
- First posted
- 2022-01-21
- Last updated
- 2022-10-28
Locations
1 site across 1 country: Hong Kong
Source: ClinicalTrials.gov record NCT05200741. Inclusion in this directory is not an endorsement.