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NCT02960594 · ClinicalTrials.gov registry record · Phase 1

hTERT Immunotherapy Alone or in Combination With IL-12 DNA Followed by Electroporation in Adults With Solid Tumors at High Risk of Relapse

A Phase 1 study, sponsored by Inovio Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
93
Enrollment target

NCT02960594: Completed Phase 1 study, sponsored by Inovio Pharmaceuticals.

NCT02960594 is a Phase 1 study that has completed, run by Inovio Pharmaceuticals. The registered enrollment target is 93 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02960594, a Phase 1 study, has completed, sponsored by Inovio Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
93 participants
Enrollment target

Study Summary

This is a Phase I, open label study to evaluate the safety, tolerability, and immunogenicity of INO-1400 or INO-1401 alone or in combination with INO-9012, delivered by electroporation in subjects with high-risk solid tumor cancer with no evidence of disease after surgery and standard therapy. Subjects will be enrolled into one of ten treatment arms. Subjects will be assessed according to standard of care. Restaging and imaging studies will be performed to assess disease relapse per NCCN guidelines. RECIST will be used to validate the findings in cases of relapse.

Interventions

  • BIOLOGICAL INO-9012
  • BIOLOGICAL INO-1400
  • BIOLOGICAL INO-1401

Trial Details

FieldValue
Enrollment Target 93 participants
Start Date 2014-12
Est. Completion 2018-11-09
Phase Phase 1
Inovio Pharmaceuticals

28 total trials

What the finished NCT02960594 record still lists

NCT02960594 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 93 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% higher).

The record links to 0 conditions, and to 3 interventions - of which INO-9012 is the first listed.

NCT02960594 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02960594 about?

NCT02960594 is a clinical study titled "hTERT Immunotherapy Alone or in Combination With IL-12 DNA Followed by Electroporation in Adults With Solid Tumors at High Risk of Relapse". This is a Phase I, open label study to evaluate the safety, tolerability, and immunogenicity of INO-1400 or INO-1401 alone or in combination with INO-9012, delivered by electroporation in subjects with high-risk solid tumor cancer with no evidence of disease after surgery and standard therapy. Subje...

What is the current status of trial NCT02960594?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 93 participants. The study started on 2014-12. Estimated completion is 2018-11-09.

What interventions are being tested in trial NCT02960594?

The interventions under investigation include: INO-9012 (BIOLOGICAL), INO-1400 (BIOLOGICAL), INO-1401 (BIOLOGICAL).

Who is sponsoring clinical trial NCT02960594?

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 NCT02960594's enrollment target sits among peer trials

93 624th of 2000 higher than 1,376 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 NCT02960594, the US trial registry maintained by the National Library of Medicine. NCT02960594 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.