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RecruitingPhase 4

Zopa Retreatment and Vector Shedding in Adults With RRP

Precigen, Inc · NCT06538480

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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
Zopa Retreatment and Vector Shedding in Adults With RRP (NCT06538480) | Bored Studies