WHO ICTRP trial
Phase I/IIa Clinical Trial to Evaluate the Safety, Tolerability and…
ChiCTR2400089762 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting
Key facts
| Trial ID | ChiCTR2400089762 |
|---|---|
| Public title | Phase I/IIa Clinical Trial to Evaluate the Safety, Tolerability and Immunogenicity of Longkoma Quadrivalent Recombinant Norovirus Vaccine (Pichia Pastoris) Implanted in Populations of 6 Weeks and Older |
| Scientific title | Phase I/IIa Clinical Trial to Evaluate the Safety, Tolerability and Immunogenicity of Longkoma Quadrivalent Recombinant Norovirus Vaccine (Pichia Pastoris) Implanted in Populations of 6 Weeks and Older |
| Primary sponsor | Guangxi Zhuang Autonomous Region Centre for Disease Control and Prevention |
| Registry | Chinese Clinical Trial Registry (ChiCTR) |
| Recruitment status | Not Recruiting |
| Study type | Interventional study |
| Phase | 1-2 |
| Countries | China |
| Conditions | Acute gastroenteritis caused by norovirus |
| Interventions | adults:low dose;adults:high dose;adults:Placebo (with aluminum);teenagers:low dose;teenagers:high dose;teenagers:Placebo (with aluminum);elderly(60 years old and above):low dose;elderly(60 years old and above):high dose;elderly(60 years old… |
| Registration date | Sep 14, 2024 |
| Target size | adults:20;adults:20;adults:20;teenagers:20;teenagers:20;teenagers:20;elderly(60… |
| Registry page | chictr.org.cn |
At a glance
- No Results available
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About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: