Codagenix Phase. Its intranasal COVID‑19 vaccine "CoviLiv" is in i

Its intranasal COVID‑19 vaccine "CoviLiv" is in international Phase 3 trials. CoviLiv is a novel intranasal live-attenuated COVID-19 vaccine candidate, derived from SARS-CoV-2/Wuhan that was synthetically engineered utilizing Codagenix’ codon pair Information on valuation, funding, cap tables, investors, and executives for Codagenix. 88 million will support activities to advance CodaVax-DENV into the clinic Farmingdale, N. Codagenix is a clinical-stage biotechnology Back to news Clinical Trials Arena 2022 / News Coverage Codagenix and SII begin subject dosing in Phase III Covid-19 vaccine trial Codagenix is combining codon deoptimization with live-attenuated viruses for a vaccine and therapeutic platform poised to transform global health. Completes Dosing for Phase 1 Trial of Live-Attenuated, Intranasal Vaccine for Respiratory Syncytial Virus (RSV) This study is a Phase 1, randomized, double-blind, placebo-controlled, dose-escalation clinical trial to evaluate the safety of and immune response to CodaVax-RSV in Codagenix will develop nOPV-maxSD vaccine candidates with its proprietary synthetic biology to further improve genetic stability FARMINGDALE, N. , June 14, 2022 /PRNewswire/ -- Codagenix Inc. Results demonstrate CoviLiv, a novel intranasal live-attenuated COVID-19 vaccine candidate, induces robust humoral and cellular immunity in healthy adults. , a clinical-stage synthetic biology company with a rational virus design platform for viral vaccines and immuno-oncology Codagenix Inc. In addition, Codagenix recently announced that the Biomedical Advanced Research and Development Authority (BARDA), part of the Administration Codagenix has concluded the dosing of subjects in its Phase I clinical trial of a universal, live-attenuated influenza vaccine, CodaVax-H1N1. , a clinical-stage synthetic biology Codagenix is moving its rational virus design platform forward with a new Phase I trial of its live attenuated respiratory syncytial virus ^ "COVI-VAC for SARS-CoV-2 (COVID-19)". with its drug pipeline, therapeutic area, technology platform, 8 clinical trials, 55 news, and 25 literature, Disease Domain:Infectious Award valued at $5. FARMINGDALE, N. , a clinical-stage synthetic biology company with a rational virus design platform for viral vaccines and immuno-oncology therapeutics, today announced that it Codagenix sees expanding horizons in vaccine development Codagenix, partnering with the Serum Institute of India, began dosing an . With completion of the STV study, Codagenix faces a late 2024 data readout following enrollment challenges in its paediatric RSV vaccine Phase I study. About Codagenix, Inc. Use the PitchBook Platform to explore the full profile. CoviLiv is being investigated in The global Phase 3 trial will evaluate the safety, efficacy, and immunogenicity of CoviLiv against circulating SARS-CoV-2 strains as compared to placebo in up to 20,000 healthy adults in This study is a Phase 1, randomized, double-blind, placebo-controlled, dose-escalation clinical trial to evaluate the safety of and immune response to CodaVax-RSV in For this initial phase, Codagenix will synthetically modify the genomes of nOPV strains to produce new nOPV-maxSD strains with intent to establish in vitro proof of concept Against the backdrop of a global push for new COVID vaccines that can provide broader and longer lasting protection, Codagenix today Codagenix has advanced multiple live attenuated vaccine candidates into clinical trials. ^ "Codagenix Announces Safety and Immunogenicity Data from Phase 1 COVID-19 Intranasal Codagenix Inc. Codagenix Announces Safety and Immunogenicity Data from Phase 1 COVID-19 Intranasal Vaccine Trial and Intent to Progress to Phase 2/3 Studies Explore Codagenix, Inc. Y. Retrieved 8 June 2021. A Based on the results of this study, a Phase 2 dose confirming study will explore efficacy during the RSV season in 2023-2024. Together with preclinical toxicology data and demonstrated clinical safety of this attenuated influenza virus after intranasal administration in healthy individuals, CodaLytic emerges as a Results demonstrate CoviLiv, a novel intranasal live-attenuated COVID-19 vaccine candidate, induces robust humoral and cellular immunity in A Phase 1 clinical trial in healthy adults reached its primary endpoint, demonstrating both safety and an anti-RSV cellular immune response. Codagenix, Inc. , July 22, 2025 /PRNewswire/ — STV is a placebo-controlled, Phase 3 safety and efficacy study with the primary endpoint of prevention of confirmed COVID-19 clinical disease. , October 24, 2023 – Codagenix Inc.

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