A Phase II Randomized, Double-blind, Placebo-controlled Clinical Trial to Evaluate the Safety and Immunogenicity of Recombinant Trivalent Subunit Rotavirus Vaccine in Healthy Infants Aged 6-12 Weeks and Healthy Toddlers Aged 7-71 Months
Latest Information Update: 25 Nov 2024
At a glance
- Drugs Subunit-rotavirus-vaccine-Maxvax-Biotechnology (Primary) ; Aluminum hydroxide
- Indications Rotavirus infections
- Focus Adverse reactions; Pharmacodynamics
- Sponsors MAXVAX Biotechnology
Most Recent Events
- 20 Nov 2024 Planned End Date changed from 1 Apr 2024 to 1 Dec 2024.
- 22 May 2023 Status changed from recruiting to active, no longer recruiting.
- 06 Feb 2023 New trial record