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NCT04925713 · ClinicalTrials.gov registry record · Phase 1

IFx-Hu2.0 for the Treatment of Patients With Skin Cancer

A Phase 1 study, sponsored by TuHURA Biosciences.

Completed
Registry status
Phase 1
Development phase
5
Enrollment target

NCT04925713: Completed Phase 1 study, sponsored by TuHURA Biosciences.

NCT04925713 is a Phase 1 study that has completed, run by TuHURA Biosciences. The registered enrollment target is 5 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04925713, a Phase 1 study, has completed, sponsored by TuHURA Biosciences.

COMPLETED
Registry status
Phase 1
Development phase
5 participants
Enrollment target

Study Summary

One hundred patients will receive IFx-Hu2.0 on an outpatient basis at a single time point in a single lesion. These patients will be assessed for any immediate adverse reactions and at Week 4 (Day 28+/-5 days) for any delayed adverse events..

Primary Outcome

Rate of Adverse Events reported per Common Terminology Criteria for Adverse Events (CTCAE) v5.0

Interventions

  • BIOLOGICAL IFx-Hu2.0

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2021-06-10
Est. Completion 2022-03-10
Phase Phase 1
TuHURA Biosciences

5 total trials

What the finished NCT04925713 record still lists

NCT04925713 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which IFx-Hu2.0 is the first listed.

NCT04925713 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04925713 about?

NCT04925713 is a clinical study titled "IFx-Hu2.0 for the Treatment of Patients With Skin Cancer". One hundred patients will receive IFx-Hu2.0 on an outpatient basis at a single time point in a single lesion. These patients will be assessed for any immediate adverse reactions and at Week 4 (Day 28+/-5 days) for any delayed adverse events..

What is the current status of trial NCT04925713?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 5 participants. The study started on 2021-06-10. Estimated completion is 2022-03-10.

What interventions are being tested in trial NCT04925713?

The interventions under investigation include: IFx-Hu2.0 (BIOLOGICAL).

Who is sponsoring clinical trial NCT04925713?

This trial is sponsored by TuHURA Biosciences, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04925713's enrollment target sits among peer trials

5 1989th of 2000 higher than 6 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 NCT04925713, the US trial registry maintained by the National Library of Medicine. NCT04925713 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.