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Re: DewDiligence post# 4769

Thursday, 10/12/2023 3:19:20 PM

Thursday, October 12, 2023 3:19:20 PM

Post# of 7254

However, prior to FDA approval this analyst had modeled the probably of success in CD at 70% (not 80%), a figure that I ridiculed in #msg-170173399.



The 70% was in a report in 2022. In March, 2023, the analyst bumped it to 80%:

Pipeline: On January 6th, 2022 the company announced the acceptance of the Daxxify sBLA to treat Cervical Dystonia (LINK), with a PDUFA date of 8/19/23. CD would represent the first therapeutic indication for Daxxify. We increase our POS to 80% from 70% and we model 2023 therapeutic revenue of $2.9mn vs. cons. $3.0mn.




























Pipeline: On January 6th, 2022 the company announced the acceptance of the Daxxify sBLA to treat Cervical Dystonia (LINK), with a PDUFA date of 8/19/23. CD would represent the first therapeutic indication for Daxxify. We increase our POS to 80% from 70% and we model 2023 therapeutic revenue of $2.9mn vs. cons. $3.0mn.
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