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Aridis Pharma Says Phase 2a Study Of AR-501 In Cystic Fibrosis Meets Endpoints

Aridis Pharmaceuticals, Inc. (ARDS) announced Monday preliminary top-line results from the randomized, double blinded, placebo-controlled Phase 2a study of AR-501, which evaluated the safety and pharmacokinetics of three ascending doses of AR-501 administered as an inhaled aerosol in cystic fibrosis (CF) patients with confirmed Pseudomonas aeruginosa bacterial and other potential infections.
Aridis Pharmaceuticals Inc More Such Health News Cystic Fibrosis Foundation Aridis Pharmaceuticals Cystic Fibrosis R 501

Aridis Enters into APEX™ Licensing and Product Discovery Agreement for Zoonotic Viruses with Kermode

Aridis Enters into APEX™ Licensing and Product Discovery Agreement for Zoonotic Viruses with Kermode News provided by Share this article Share this article LOS GATOS, Calif., March 8, 2021 /PRNewswire/ -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS) today announced that it has entered into an out-licensing and product discovery agreement with Kermode Biotechnologies, Inc. Kermode works on vaccines and mAbs for zoonotic viruses, which are animal viruses that have the ability to infect humans. ...
Aridis Pharma Dan Chen Vu Truong Exchange Commission Aridis Pharmaceuticals Kermode Biotechnologies Inc

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