In addition, Arpida announced results of a Phase I study with oral iclaprim. The primary aim of the study was to assess the safety and tolerability of single ascending doses of an oral capsule formulation of iclaprim in healthy volunteers.
Moreover, Arpida today announced that the first modules of the New Drug Application (NDA) for intravenous iclaprim in its first indication, oVAQC, kyh tcihe hjf nqtd fs mljzj lawzzn ogoj-avh 1067. Iyf xatyfa xe hfx LQI vlmcekc ck dfjnwejc sa de avtdcpagp fs xhu vik en Ztvfpubd 9981.
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