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: Ritu Baral - TD Cowen - Analyst
: So, Wes -- sorry, I'm covering analyst Ritul Baral with TD Cowen. Maybe you can talk to us a little bit about your conversations with the FDA on the
trial design and the novel endpoint for this SELVA study, their understanding of the unmet need, and their buy-in as it stands, understanding that
they never give final buy-in until you get the effect size and blah, blah, blah.
Question: Ritu Baral - TD Cowen - Analyst
: So alongside -- you're going to make your announcement about additional indications later. But how are you thinking about the strategy behind
additional indications? You're going to keep specializing in rare derm, but what are other characteristics of the indications that makes sense for
Palvella?
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MARCH 04, 2025 / 7:30PM, PVLA.OQ - Palvella Therapeutics Inc at TD Cowen Healthcare Conference
Question: Ritu Baral - TD Cowen - Analyst
: Competi -- so little to no competition.
Question: Ritu Baral - TD Cowen - Analyst
: And then, what other molecules are you investigating as future candidates? What are some of the biochemical features that best fit with QTORIN
or best fit with QTORIN versus any other formulation technology?
Question: Ritu Baral - TD Cowen - Analyst
: And besides the QTORIN platform, are there any other in-house R&D currently underway?
Question: Ritu Baral - TD Cowen - Analyst
: Great. Thank you, Wes.
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MARCH 04, 2025 / 7:30PM, PVLA.OQ - Palvella Therapeutics Inc at TD Cowen Healthcare Conference
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