Evotec AG: Evotec Starts Clinical Development of Chikungunya Antibody together with NIAID and Leading Academic Research Organisation
DEVELOPMENT OF EVT894 BY EVOTEC TOGETHER WITH ITS PARTNERS NIAID AND DUKE CLINICAL RESEARCH INSTITUTE
ADDRESSING UNMET MEDICAL NEEDS IN GLOBAL HEALTH
HAMBURG, GERMANY / ACCESSWIRE / January 28, 2021 / Evotec SE (Frankfurt Stock Exchange: EVT, MDAX/TecDAX, ISIN: DE0005664809) today announced that EVT894, a monoclonal antibody to treat and potentially prevent chikungunya virus infections, has entered clinical development.
The Phase I, randomised, double-blind, single centre, single dose escalation study to evaluate the safety, pharmacokinetics, and immunogenicity of EVT894 vs placebo in healthy volunteers (five dose-cohorts of 8 subjects) is sponsored and funded by the National Institute of Allergy and Infectious Diseases ( NIAID ), part of the National Institutes of Health with funds from a Phase I Clinical Trial Units for Therapeutics programme awar
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