The following is excerpted from the question-and-answer section of the transcript.
(Questions from industry analysts are provided in full, but answers are omitted - download the transcript to see the full question-and-answer session)
Question: Aydin Huseynov - Ladenburg Thalmann & Co. Inc. - Analyst
: Good morning, everyone. Good morning, Linda, AJ. Congratulations with the great progress. Sorry for the background noise here. So want to clarify,
regarding the reasons for the dropouts, could you just clarify this? And how these dropouts will compare to other Duchenne trials, if you could, at
all, compare to this? Thank you.
Question: Aydin Huseynov - Ladenburg Thalmann & Co. Inc. - Analyst
: Thank you, appreciate that. And could you comment on any interactions you may have had with the European agency at all?
Question: Aydin Huseynov - Ladenburg Thalmann & Co. Inc. - Analyst
: Got it, got it. And the last one, so I'm just trying to understand what you guys will do beyond (technical difficulty) drug --
Question: Aydin Huseynov - Ladenburg Thalmann & Co. Inc. - Analyst
: I'm sorry, could you hear me now?
Question: Aydin Huseynov - Ladenburg Thalmann & Co. Inc. - Analyst
: Yeah, so, yes, yeah, so the question is, any plans beyond Duchenne, with your specific drug? Thank you.
Question: Aydin Huseynov - Ladenburg Thalmann & Co. Inc. - Analyst
: Perfect, thanks so much for taking my questions. And congratulations with this progress, with clarifying the FDA path, this is significant for me.
Thank you so much.
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