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Adjuvant PRGN-2012 in Adult Patients With Recurrent Respiratory Papillomatosis

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NCT04724980

Sponsored by Precigen, Inc (industry) · PGEN — their whole pipeline →. With National Cancer Institute (NCI).

Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
38actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-03-16actualWhen the study began enrolling
Primary completion2024-06-05actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-06-05estimatedThe whole study's end, after follow-up
First posted2021-01-26actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-06-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Recurrent Respiratory Papillomatosis
  • Papillomavirus Infections
  • Papillomaviridae

Interventions

  • Drug: PRGN-2012 - Phase I; Dose Level 1
  • Drug: PRGN-2012 - Phase I; Dose Level 2
  • Drug: PRGN-2012 - Phase II; Dose Level 2

Primary outcomes

what the primary-completion date above is the date OF
Determine the percentage of subjects with a complete response following treatment with PRGN-2012
measured 1 year
Determine the incidence of dose limiting toxicities to evaluate safety and identify RP2D of PRGN-2012
measured 28 days

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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