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Active, not recruiting Phase 3 Interventional

SELVA: A Phase 3 Study Evaluating QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Microcystic Lymphatic Malformations

ClinicalTrials.gov ID: NCT06239480

Public ClinicalTrials.gov record NCT06239480. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 4:52 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

SELVA: A Multicenter, Phase 3 Baseline-Controlled Study Evaluating the Safety and Efficacy of QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Microcystic Lymphatic Malformations

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

SELVA: A Multicenter, Phase 3 Baseline-Controlled Study Evaluating the Safety and Efficacy of QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Microcystic Lymphatic Malformations The main purpose of this study is to assess the change in microcystic lymphatic malformations IGA after 24 weeks of treatment with QTORIN 3.9% Rapamycin Anhydrous Gel in approximately 40 participants with microcystic lymphatic malformations. Efficacy will be evaluated at 24 weeks and patients have the option of continuing on treatment for \>24 weeks.

Study identification

NCT ID
NCT06239480
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Palvella Therapeutics, Inc.
Industry
Enrollment
51 participants

Conditions and interventions

Eligibility (public fields only)

Age range
3 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2024 (Actual)
Primary completion
Jan 14, 2026 (Actual)
Completion
Jul 2026 (Estimated)
Last update posted
Mar 27, 2026

2024 – 2026

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Children's Hospital of Orange County Irvine California 92612 —
Stanford University Palo Alto California 94305 —
Children's Healthcare of Atlanta Atlanta Georgia 30342 —
Minnesota Clinical Study Center New Brighton Minnesota 55112 —
Mayo Clinic Rochester Minnesota 55905 —
Vascular Birthmark Institute New York New York 10016 —
University of North Carolina Chapel Hill North Carolina 27516 —
Cincinnati Children's Hospital Cincinnati Ohio 45229 —
Cleveland Clinic Cleveland Ohio 44195 —
Penn State Hershey Medical Center Hershey Pennsylvania 17033 —
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 —
Vanderbilt Children's Hospital Nashville Tennessee 37232 —
University of Texas, Dell Children's Austin Texas 78723 —
Texas Children's Hospital Houston Texas 77030 —
University of Utah Health Salt Lake City Utah 84113 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06239480, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 27, 2026 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06239480 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →