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Sanofi’s Chlamydia Vaccine Candidate Granted Fast Track Designation by FDA

Following a promising pre-clinical program, Sanofi is planning a phase 1/2 randomized, clinical study.

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By: Charlie Sternberg

Associate Editor

The US Food and Drug Administration (FDA) has granted fast track designation to Sanofi’s mRNA vaccine candidate for the prevention of chlamydia infection. The decision was based on the potential of the vaccine candidate to address a serious condition and address an unmet public health need. The chlamydia vaccine candidate is designed to protect against primary genital tract infection and reinfection by the bacterium Chlamydia trachomatis. Following a promising pre-clinical program, Sanofi is ...

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