Pfizer and Valneva's Lyme Disease Vaccine Candidate Moves to EMA Review
Pfizer and Valneva’s investigational Lyme disease vaccine PF-07307405 has received EMA validation for its Marketing Authorization Application, triggering the European regulatory review.
Marketing Authorization Application | 17/08/2026 | By News Bureau
Philogen Resubmits EMA Marketing Application for Melanoma Therapy Nidlegy with Updated Phase 3 Data
Philogen has resubmitted its EMA marketing application for investigational melanoma therapy Nidlegy, supported by updated Phase 3 clinical data demonstrating reduced risk of relapse or death and an extended patient follow-up period.
Marketing Authorization Application | 28/07/2026 | By News Bureau | 136
EMA Approves Marketing Authorization Application of Nidlegy
Philogen and Sun Pharmaceutical Industries Ltd. have announced that the European Medicines Agency (EMA) validated the submission of the Marketing Authorization Application (MAA) for Nidlegy.
Marketing Authorization Application | 05/07/2024 | By Aishwarya | 548
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