CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 5 enrolled
Drug / intervention
IFx-Hu2.0biological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04925713
NCT04925713Phase 1Completed

Phase 1 Trial of IFx-Hu2.0 to Evaluate Safety in Patients With Skin Cancer

TuHURA Biosciences, Inc.·interventional·Posted Jun 14, 2021·Updated Aug 2, 2024

In Brief

A Phase 1 clinical trial evaluating IFx-Hu2.0 for Cutaneous Squamous Cell Carcinoma and Basal Cell Carcinoma. Completed, enrolled 5 participants across 1 site.

Detailed 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..

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
20222023202420252026
First PostedJun 14, 2021
Enrollment StartJun 10, 2021
Primary CompletionOct 7, 2021
Study CompletionMar 10, 2022
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 5.0 years ago

Interventions

IFx-Hu2.0biological

The investigational drug product IFx-Hu2.0 is composed of the drug substance pAc/emm55 (pDNA) complexed with the two excipients in vivo-jetPEI® (linear polyethylenimine), a transfection reagent, and dextrose, a pDNA/polyethylenimine complex stabilizer. Therapeutic Classification: * Immunomodulatory Agent Route of Administration: * Intralesional (i.e. injection of cutaneous, subcutaneous or lymph nodal lesions) Mechanism of Action: * Injection of IFx-Hu2.0 into the lesion facilitates the expression of the immunogenic Emm55 protein by the tumor cells. Physiological Effect: * Expression of the emm55 gene by the tumor cells triggers immune recognition of tumor-specific and -associated antigens which leads to innate and adaptive immune responses.