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Palvella Therapeutics Appoints Rare Disease Senior Executive Elaine J. Heron, PhD to Board of Directors

October 6, 2018

“Pachyonychia congenita (PC) is a life-altering genetic disease which dramatically limits patients’ ability to ambulate and perform everyday functional activities,” stated Dr. Heron. “Palvella’s lead program PTX‑022 (novel, high-strength rapamycin topical formulation, optimized for dermal targeting) has significant potential to address this serious unmet need that currently has no approved treatments. I look forward to applying my background in rare diseases in supporting Palvella’s efforts to advance PTX-022 through late stage clinical development and commercialization.”

Read the full press release.

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PACHYONYCHIA CONGENITA PROJECT

P.O. Box 17850
Holladay, UT 84117

info@pachyonychia.org

801-987-8758

EIN 68-0567493

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