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EMA Begins Assessment of Pfizer and Valneva’s PF‑07307405 Lyme Vaccine Application

Pfizer logoPfizer
Sig2.68Sen+3.24Env0.00Soc+2.05Gov+0.62
Valneva SE logoValneva SE
Sig2.32Sen+4.20Env0.00Soc+1.80Gov+0.80

The EMA will begin assessing Pfizer and Valneva’s PF‑07307405 Lyme disease vaccine application. The submission draws on Phase 3 VALOR results in people aged five and older, with efficacy above 70% and no safety concerns reported. Earlier March topline results did not meet the primary endpoint due to fewer cases than expected. Pfizer will manufacture and commercialize under the co-development deal.

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