Zopapogene imadenovec (Zopa)
DrugZopa will be administered as 4 subcutaneous administrations over a 12-week interval.
NCT Number: NCT06538480
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 4
Winship Cancer Institute, Emory University, Atlanta, Georgia, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Zopa will be administered as 4 subcutaneous administrations over a 12-week interval.
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
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.
Time frame: 3 years following last administration
Determine the interval to the first debulking procedure following retreatment with Zopapogene imadenovec (Zopa).
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.
Contact information is provided by the study sponsor or research team.
Precigen, Inc
Industry
Open-Label Study of Zopapogene Imadenovec Retreatment and Vector Shedding Evaluation in Adult Patients With Recurrent Respiratory Papillomatosis
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