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NCT05976828 · ClinicalTrials.gov registry record · Phase 1

IBRX-042 In Participants With HPV-Associated Tumors

A Phase 1 study of HPV-Related Carcinoma, sponsored by ImmunityBio.

Active
Registry status
Phase 1
Development phase
12
Enrollment target
3
Study locations

NCT05976828 is a Phase 1 study of HPV-Related Carcinoma that is active but no longer recruiting, run by ImmunityBio. The registered enrollment target is 12 participants, below the 154-participant average among 10 other HPV-Related Carcinoma trials with a reported enrollment target (92% lower). The trial reports 3 study locations across 2 states.

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The verdict

NCT05976828, a Phase 1 study of HPV-Related Carcinoma, is active but no longer recruiting, sponsored by ImmunityBio.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
12 participants
Enrollment target
3
Study locations

Study Summary

The goal of this clinical trial is to determine the maximum tolerated dose and to find out the side effects of a drug called IBRX-042 at different dose levels in patients with recurrent or progressive Human Papillomavirus (HPV) associated tumors. The main questions it aims to answer are: * What is the maximum tolerated dose of IBRX-042? * How well does the study drug treat cancer? * What effects the study drug may have on the human body and cancer? Participants will receive IBRX-042 at one of three dose levels every 3 weeks for a total of 3 injections. Participants will undergo tests, exams, and procedures that are part of standard of care and for study purposes. IBRX-042 will be administered by injection every 3 weeks for a total of 3 injections.

Conditions Studied

Interventions

  • DRUG IBRX-042

Study Locations (3)

Texas

  • Texas Oncology Austin Central - Austin
  • The University of Texas - MD Anderson Cancer Center - Houston

California

  • Chan Soon-Shiong Institute for Medicine (CSSIFM) - El Segundo

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2024-06-14
Est. Completion 2033-08-14
Phase Phase 1

Sponsor

ImmunityBio

46 total trials

What the Registry Record Tells You About NCT05976828

The ClinicalTrials.gov registry entry for NCT05976828 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 154-participant average among 10 other HPV-Related Carcinoma trials with a reported enrollment target (92% lower). The listed sponsor is ImmunityBio, which has 46 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with HPV-Related Carcinoma appearing as the primary indexed condition, and to 1 intervention - of which IBRX-042 is the first listed.

NCT05976828 reports 3 study locations spanning 2 distinct geographic areas - top geographies include Texas, California.

Frequently Asked Questions

What is clinical trial NCT05976828 about?

NCT05976828 is a clinical study titled "IBRX-042 In Participants With HPV-Associated Tumors". The goal of this clinical trial is to determine the maximum tolerated dose and to find out the side effects of a drug called IBRX-042 at different dose levels in patients with recurrent or progressive Human Papillomavirus (HPV) associated tumors. The main questions it aims to answer are: * What is ...

What is the current status of trial NCT05976828?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2024-06-14. Estimated completion is 2033-08-14.

What conditions does trial NCT05976828 study?

This clinical trial studies the following conditions: HPV-Related Carcinoma.

What interventions are being tested in trial NCT05976828?

The interventions under investigation include: IBRX-042 (DRUG).

Who is sponsoring clinical trial NCT05976828?

This trial is sponsored by ImmunityBio, which has 46 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05976828 being conducted?

This trial has 3 study locations across California, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.