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Recruiting NCT06412172

NCT06412172 The Natural History and Biological Study of Pulmonary Recurrent Respiratory Papillomatosis (pRRP)

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Clinical Trial Summary
NCT ID NCT06412172
Status Recruiting
Phase
Sponsor Massachusetts General Hospital
Condition Recurrent Respiratory Papillomatosis
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2024-04-15
Primary Completion 2026-04-14

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 99 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2024-04-15 with a primary completion date of 2026-04-14.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Recurrent respiratory papillomatosis (RRP) is an orphan disease that affects approximately 20,000 people in the United States and is caused by infection with human papillomavirus (HPV) types 6 and 11. Since RRP is an orphan disease, it is an understudied disease entity with correspondingly few treatment options. The investigators hypothesize that by understanding the biology of RRP and the failed host immune responses against HPV, novel and rational therapies can be developed. This study will examine the genetic and immunologic alterations found in these rare tumors and distant metastatic involved sites (such as the lung) in patients diagnosed with RRP.

Eligibility Criteria

Inclusion Criteria: * History of HPV-associated Recurrent Respiratory Papillomatosis * Has pulmonary lesions Exclusion Criteria: * None

Contact & Investigator

Central Contact

Sara Pai, MD, PhD

✉ RRPBiorepository@yale.edu

📞 203-785-5820

Principal Investigator

Sara Pai

PRINCIPAL INVESTIGATOR

Yale University

Frequently Asked Questions

Who can join the NCT06412172 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 99 Years, studying Recurrent Respiratory Papillomatosis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06412172 currently recruiting?

Yes, NCT06412172 is actively recruiting participants. Contact the research team at RRPBiorepository@yale.edu for enrollment information.

Where is the NCT06412172 trial being conducted?

This trial is being conducted at New Haven, United States.

Who is sponsoring the NCT06412172 clinical trial?

NCT06412172 is sponsored by Massachusetts General Hospital. The principal investigator is Sara Pai at Yale University. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology