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NCT Number: NCT06538480

Zopa Retreatment and Vector Shedding in Adults With RRP

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Winship Cancer Institute, Emory University, Atlanta, Georgia, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Zopapogene imadenovec (Zopa)

Drug

Zopa will be administered as 4 subcutaneous administrations over a 12-week interval.

Primary outcomes

  1. Cohort 1 Vector shedding

    Time frame: Up to 6 weeks following last administration, with additional collections if needed until two consecutive measurements at or below limit of detection

    Magnitude and duration of Zopa vector shedding measured in urine, fecal, skin, and nasal tissue

  2. Cohort 2 Complete Response Rate

    Time frame: 12 months following last administration

    Percentage of subjects achieving a complete response defined as no clinically indicated debulking procedures during the 12 months following completion of Zopa retreatment.

Secondary outcomes

  1. Interval to First Debulking Procedure (Cohort 2)

    Time frame: 3 years following last administration

    Determine the interval to the first debulking procedure following retreatment with Zopapogene imadenovec (Zopa).

  2. Safety and Tolerability of Zopa (Cohort 1 and Cohort 2)

    Time frame: Up to 28 days after last administration, with extended monitoring during follow-up.

    Assess the safety and tolerability of Zopa in adult subjects with recurrent respiratory papillomatosis (RRP), including incidence and severity of adverse events graded per CTCAE v5.0.

Study contacts

Contact information is provided by the study sponsor or research team.

Head of Clinical Operations

CONTACT

[email protected]

301-556-9900

Sponsors and collaborators

Lead sponsor

Precigen, Inc

Industry

Registry information

Official study title

Open-Label Study of Zopapogene Imadenovec Retreatment and Vector Shedding Evaluation in Adult Patients With Recurrent Respiratory Papillomatosis

Important dates

Study start
2024
Primary completion
2027
Study completion
2028
First posted
Aug 5, 2024
Registry last updated
Dec 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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