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NanoViricides Reports that the Phase I NV-387 Clinical Trial is Completed Successfully and Data Lock

SHELTON, CT / ACCESSWIRE / April 30, 2024 / NanoViricides, Inc. (NYSE Amer:NNVC) (the "Company"), a global leader in broad-spectrum antiviral nanomedicines, reports that the Phase I Clinical Trial of NV-387 is completed successfully and data lock is expected soon.The Phase 1 clinical trial, protocol number...
United States Karveer Meditech Nirsevimab Beyfortus Nanoviricides Inc Development Towards Regulatory Approval Exchange Commission

ARS Pharma Submits Response For Neffy MAA To EMA's CHMP, Signs License Deal With CSL Seqirus

ARS Pharmaceuticals (SPRY), Tuesday announced the submission of Day 180 response for Neffy's Marketing Authorization Application to the Committee for Medicinal Products for Human Use of the European Medicines Agency, expecting to receive the opinion on the drug in the second quarter of 2024.
New Zealand Committee For Medicinal Products Human Use Marketing Authorization Application Medicinal Products Human Use European Medicines Agency

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Bavarian Nordic Initiates Rolling Submission of Biologics License Application with FDA for its Chikungunya Vaccine Candidate

COPENHAGEN, Denmark, April 29, 2024 – Bavarian Nordic A/S today announced that it has initiated the rolling submission process with the U.S. Food and Drug Administration for a Biologics License...
Graham Morrell Paul Chaplin Committee For Medicinal Products Human Use Drug Administration Company Announcement Bavarian Nordic

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