GREY:ATBPF - Post by User
Comment by
RalphRalphon Jul 23, 2019 5:22pm
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Post# 29952685
RE:RE:RE:RE:RE:A new prospectus
RE:RE:RE:RE:RE:A new prospectusFrom today's prospectus, "Use of Proceeds" section:
"The reproductive toxicology studies for ATB-346 will be conducted in animals and are a key regulatory requirement for drug approval. The first tranche of these studies are expected to commence in calendar Q4 2019 and take approximately six months to complete. The regulatory consulting fees are for preparation for the Company’s Investigational New Drug (“IND”) filing with the FDA, and pre-IND and end-of-Phase 2 meetings with the FDA. The Company has retained a leading regulatory consulting agency based out of Washington, DC to support this preparatory work over the next six months. The health economics, payor and market opportunity studies will utilize industry standard methodology to formally characterize the commercial potential of ATB-346 based upon primary (physician and payor interviews) and secondary research. The studies are expected to take approximately 2-3 months to complete. The Company believes that the findings of these studies should be valuable in future partnering discussions."