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NCT05775887
A FIRST IN HUMAN TO EVALUATE THE SAFETY AND IMMUNOGENICITY OF SARS-CoV-2 UQSC2 VACCINE IN HEALTHY ADULTS.
Phase 1 trial testing UQSC2 Vaccine in COVID-19 in 70 participants. Completed in 16 December 2023.
2 December 2023
Quick facts
| Lead sponsor | The University of Queensland |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | prevention |
| Enrollment | 70 |
| Start date | 8 May 2023 |
| Primary completion | 2 December 2023 |
| Estimated completion | 16 December 2023 |
| Sites | 1 location across Australia |
Drugs / interventions tested
- UQSC2 Vaccine — full drug profile →
- NVX-CoV2373 vaccine — full drug profile →
Conditions studied
- COVID-19 — all drugs for COVID-19 →
Sponsor
The University of Queensland
Who can join
Adults 18 to 50, any sex, with COVID-19. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This will be a single centre, Phase 1, First-In-Human , Randomized, Active-controlled (2- arm) Double-blind, single dose, parallel design study. The study will be conducted in a young healthy adult population aged ≥ 18 - ≤ 50 years. This study will consist of a single cohort of 70 subjects (35 receiving a single dose of UQSC2 vaccine and 35 subjects receiving a single dose of a TGA (Therapeutic Goods Administration) registered SARS-CoV-2 vaccine NVX-CoV2373).
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
A second-generation molecular clamp stabilised bivalent candidate vaccine for protection against diseases caused by respiratory syncytial virus and human metapneumovirus.
Young A, Kolekar S, Mendoza CA, Jaberolansar N, et al · · 2025 · cited 4× · PMID 40674411 · DOI 10.1371/journal.ppat.1013312 -
Long-term safety and immunogenicity of an MF59-adjuvanted spike glycoprotein-clamp vaccine for SARS-CoV-2 in adults aged 18-55 years or ≥56 years: 12-month results from a randomised, double-blind, placebo-controlled, phase 1 trial.
Chappell KJ, Mordant FL, Amarilla AA, Modhiran N, et al · · 2023 · cited 3× · PMID 37865043 · DOI 10.1016/j.ebiom.2023.104842 -
Safety and Immunogenicity of a Severe Acute Respiratory Syndrome Coronavirus 2 Spike Subunit Vaccine Stabilized in the Prefusion Conformation by a Second-Generation Molecular Clamp and Evaluated in Adults Aged 18-55 Years: A Randomized, Double-Blind, Active Comparator, Phase I Tr
Chappell KJ, Mordant FL, Amarilla AA, Modhiran N, et al · · 2026 · PMID 41285172 · DOI 10.1093/infdis/jiaf568
Verify or expand the search:
- PubMed search for NCT05775887
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other The University of Queensland trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05775887 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by The University of Queensland
- Last refreshed: 6 March 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05775887.
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