Zopa Retreatment and Vector Shedding in Adults With RRP
Precigen, Inc · NCT06538480
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 4
- Target enrollment
- 30
- US sites recruiting
- 3
- Study start
- July 11, 2024
- Record last updated
- December 15, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This open-label study evaluates safety, vector shedding, and retreatment efficacy of Zopapogene imadenovec (Zopa) in adults with recurrent respiratory papillomatosis (RRP). Two cohorts will be enrolled (n=30): Cohort 1 to assess the magnitude and duration of adenoviral vector shedding in urine, feces, skin, and nasal tissue; Cohort 2 to assess the complete response rate following retreatment.
Being studied: Zopapogene imadenovec (Zopa)
Conditions: Recurrent Respiratory Papillomatosis; Papillomavirus Infection; Papillomaviridae
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Key Inclusion Criteria
- Age 18 years and older.
- Clinical diagnosis of recurrent respiratory papillomatosis with histological confirmation of papilloma.
- Cohort 1: Treatment-naïve with respect to Zopa.
- Cohort 2: Received a minimum of four administrations of Zopa at 5 × 10\^11 PU per injection and require clinically indicated debulking procedures.
- Presence of laryngotracheal papillomas accessible for endoscopic cleanout.
- ECOG performance status 0 or 1.
- Sexually active participants of reproductive potential must agree to use contraception during treatment and for 120 days for males and 6 months for females after last dose.
- Ability to understand and sign informed consent.
Key Exclusion Criteria
- Conditions or therapies that increase risk or interfere with participation per investigator judgment.
- Systemic corticosteroids >10 mg prednisone equivalent or other immunosuppressive medications within 14 days prior to dosing.
- Other systemic RRP treatments or investigational agents within 30 days.
- History of heparin-induced thrombocytopenia or vaccine-induced thrombotic thrombocytopenia.
- Active uncontrolled HIV, hepatitis B, or hepatitis C infection.
- Pregnant or nursing women.
- Known allergy to any study drug component.
Recruiting US locations
Winship Cancer Institute, Emory University
Atlanta, GA 30322
Site contact: Mosope Oyewole, CRC · 404-778-5351 · mdoyewo@emory.edu
National Institute of Health
Bethesda, MD 20892
Site contact: Shannon Householder, RN · 240-656-8771 · Shannon.householder@nih.gov
University of Cincinnati
Cincinnati, OH 45267
Site contact: Rebecca Reinert · 513-558-1719 · gibsonrk@ucmail.uc.edu
Study contacts (from the official record)
- Head of Clinical Operations · 301-556-9900 · clinicaltrials@precigen.com