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mRNA-1172 (also known as V172) is an mRNA-based vaccine candidate developed for the prevention of respiratory syncytial virus (RSV) infection. It was originally part of a strategic collaboration between Moderna and Merck initiated in 2015. The vaccine utilizes Moderna's lipid nanoparticle (LNP) technology to deliver mRNA encoding a stabilized version of the RSV fusion (F) glycoprotein in its prefusion conformation (preF). Specifically, mRNA-1172 was designed as a next-generation version of mRNA-1777, incorporating a single-chain RSV F protein with interprotomer disulfides to enhance structural stability and improve the induction of neutralizing antibodies. In October 2020, Moderna regained all global rights to the program from Merck, which shifted its focus to RSV antibody programs. The candidate has been evaluated in Phase 1 clinical trials for both adult and pediatric populations, serving as a precursor to Moderna's later approved RSV vaccine, mRNA-1345 (mRESVIA).
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