This study evaluates the safety and efficacy of PTX-022 (sirolimus) Topical Gel 3.9% w/w in the treatment of Microcystic Lymphatic Malformations. The participant will receive 3 months of PTX-022 treatment by the end of the study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
Safety and Efficacy of PTX-022 in the Treatment of Microcystic Lymphatic Malformations
Arkansas Children's Hospital
Little Rock, Arkansas, United States
Stanford University
Palo Alto, California, United States
Minnesota Clinical Study Center
Fridley, Minnesota, United States
Vascular Birthmark Institute
New York, New York, United States
Incidence of Treatment-Emergent Adverse Events
Time frame: 4 months
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Cincinnati Children's Hospital
Cincinnati, Ohio, United States
Oregon Health and Science University
Portland, Oregon, United States
Children's Hospital of Pennsylvania (CHOP)
Philadelphia, Pennsylvania, United States