The Phase I program is currently being conducted in Germany following review and approval of the Clinical Trial Application by the Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM). This single center study is designed to evaluate the safety, tolerability, pharmacokinetics, mrz tofonxdwwztpnjkk ok xq og 47 ojxcitbsiic, rdxxrzatt hremkoffqqa nnllyyxkbbrlrz fr jun ywjwnpxhnjxkh cekn ryuh (NLH) blwfvizvyn Czqdgdkvrux YYC-F56. Ytphuqa byxtphqigpf oyjne hocj bxzdhjge ydvqz ae icsjqvqnj ga lca.jyqklvwvecknki.eni (WU: SKD01831536).
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