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Recurrent Respiratory Papillomatosis (RRP)Rare diseaseBiologicalPhase 1, Phase 2

What this study is

The investigators propose the study titled "Efficacy of booster injection with Gardasil-9 vaccine on intersurgical interval (ISI) for adults with recurrent respiratory papillomatosis (RRP)".

Recurrent respiratory papillomatosis (RRP) is a human papilloma virus (HPV) mediated disease of recurrent benign papillomas within the aerodigestive tract. While the foundation of treatment remains surgical debulking and occasionally adjuvant therapies such as cidofovir and bevacizumab, there remains a population of patients suffering from aggressive disease recurrence despite treatment.

Multiple studies have demonstrated treatment benefit in the form of an increase in intersurgical interval (ISI), following Gardasil vaccination. While adjuvant vaccination has favorably reduced recurrence of RRP and improved time course of disease recurrence for previously unvaccinated RRP patients, there remains a clinical population of adult patients suffering from persistent RRP that have previously undergone the Gardasil 3-vaccine series. Additionally, recent studies suggest a waning effect of Gardasil vaccination on ISI at longer time points.

Therefore, the investigators propose administering GARDASIL®9 (Human Papillomavirus 9-valent Vaccine, Recombinant) 0.5-mL suspension for injection as a one-time "booster" dose to adult patients >18 years of age, who have previously completed the 3-course vaccination series.

What's being tested

  • GARDASIL®9 (Human Papillomavirus 9-valent Vaccine, Recombinant)

    Intervention · BIOLOGICAL

    Administration of Gardasil-9 vaccine as booster dose following 3-dose vaccine series in patients with RRP.

Study details

Official title
Efficacy of Booster Injection With Gardasil-9 Vaccine on Intersurgical Interval (ISI) for Adults With Recurrent Respiratory Papillomatosis (RRP)
Sponsor
Ohio State University
Conditions
Recurrent Respiratory Papillomatosis (RRP)
Enrolling
50 people
Starts
2026-12-01
Est. completion
2035-04-01
Design
Open-label, single group, Phase 1, Phase 2
Record
View on ClinicalTrials.gov ↗