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The designation **rotavirus vaccine-PATH-malaria** refers to the live-attenuated oral rotavirus vaccine (specifically the pentavalent formulation known as **ROTASIIL** or the monovalent **ROTAVAC**) as utilized in clinical trials sponsored by **PATH** to evaluate its co-administration and scheduling with malaria vaccines, such as **R21/Matrix-M**. Developed through partnerships between PATH and Indian manufacturers (Serum Institute of India for ROTASIIL and Bharat Biotech for ROTAVAC), these vaccines are designed to prevent severe gastroenteritis caused by rotavirus infection in infants. In the context of malaria research, studies like the R21/Matrix-M Schedule Optimization trial (NCT05483972) assess the safety and immunogenicity of giving these rotavirus vaccines alongside malaria candidates to ensure that the immune response to the malaria vaccine does not interfere with the protective efficacy of standard childhood immunizations.
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