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NCT02241369 · ClinicalTrials.gov registry record · Phase 1

Immunotherapy in Subjects With HPV-6 Associated Aerodigestive Precancerous Lesions and Malignancies

A Phase 1 study, sponsored by Inovio Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
3
Enrollment target

NCT02241369: Completed Phase 1 study, sponsored by Inovio Pharmaceuticals.

NCT02241369 is a Phase 1 study that has completed, run by Inovio Pharmaceuticals. The registered enrollment target is 3 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02241369, a Phase 1 study, has completed, sponsored by Inovio Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
3 participants
Enrollment target

Study Summary

This is a Phase I, open-label study to evaluate the safety, tolerability, and immunogenicity of INO-3106 alone or in combination with INO-9012 DNA vaccines delivered by Electroporation to subjects with HPV6 associated aerodigestive precancerous lesions and malignancies.

Interventions

  • BIOLOGICAL INO-3106, INO-9012

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2014-05
Est. Completion 2018-09
Phase Phase 1
Inovio Pharmaceuticals

28 total trials

What the finished NCT02241369 record still lists

NCT02241369 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which INO-3106, INO-9012 is the first listed.

NCT02241369 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02241369 about?

NCT02241369 is a clinical study titled "Immunotherapy in Subjects With HPV-6 Associated Aerodigestive Precancerous Lesions and Malignancies". This is a Phase I, open-label study to evaluate the safety, tolerability, and immunogenicity of INO-3106 alone or in combination with INO-9012 DNA vaccines delivered by Electroporation to subjects with HPV6 associated aerodigestive precancerous lesions and malignancies.

What is the current status of trial NCT02241369?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 3 participants. The study started on 2014-05. Estimated completion is 2018-09.

What interventions are being tested in trial NCT02241369?

The interventions under investigation include: INO-3106, INO-9012 (BIOLOGICAL).

Who is sponsoring clinical trial NCT02241369?

This trial is sponsored by Inovio Pharmaceuticals, which has 28 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02241369's enrollment target sits among peer trials

3 1999th of 2000 higher than 1 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02241369, the US trial registry maintained by the National Library of Medicine. NCT02241369 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.