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NCT05698199 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Safety, Tolerability, Immunogenicity and Preliminary Efficacy of ITI-1001 In Patients With Newly Diagnosed Glioblastoma (GBM)

A Phase 1 study of Glioblastoma, sponsored by Immunomic Therapeutics.

Active
Registry status
Phase 1
Development phase
10
Enrollment target
1
Study location

NCT05698199 is a Phase 1 study of Glioblastoma that is active but no longer recruiting, run by Immunomic Therapeutics. The registered enrollment target is 10 participants, below the 109-participant average among 199 other Glioblastoma trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05698199, a Phase 1 study of Glioblastoma, is active but no longer recruiting, sponsored by Immunomic Therapeutics.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

This Phase I clinical trial will evaluate the safety, tolerability, immunogenicity, and preliminary efficacy of 8 mg ITI-1001 in participants with newly diagnosed glioblastoma (GBM).

Conditions Studied

Interventions

  • DRUG ITI-1001

Study Locations (1)

Massachusetts

  • Dana-Farber Cancer Institute - Boston

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2023-08-21
Est. Completion 2026-03
Phase Phase 1

Sponsor

Immunomic Therapeutics

6 total trials

What the Registry Record Tells You About NCT05698199

The ClinicalTrials.gov registry entry for NCT05698199 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 109-participant average among 199 other Glioblastoma trials with a reported enrollment target (91% lower). The listed sponsor is Immunomic Therapeutics, which has 6 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Glioblastoma appearing as the primary indexed condition, and to 1 intervention - of which ITI-1001 is the first listed.

NCT05698199 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT05698199 about?

NCT05698199 is a clinical study titled "Study to Evaluate the Safety, Tolerability, Immunogenicity and Preliminary Efficacy of ITI-1001 In Patients With Newly Diagnosed Glioblastoma (GBM)". This Phase I clinical trial will evaluate the safety, tolerability, immunogenicity, and preliminary efficacy of 8 mg ITI-1001 in participants with newly diagnosed glioblastoma (GBM).

What is the current status of trial NCT05698199?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2023-08-21. Estimated completion is 2026-03.

What conditions does trial NCT05698199 study?

This clinical trial studies the following conditions: Glioblastoma.

What interventions are being tested in trial NCT05698199?

The interventions under investigation include: ITI-1001 (DRUG).

Who is sponsoring clinical trial NCT05698199?

This trial is sponsored by Immunomic Therapeutics, which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05698199 being conducted?

This trial has 1 study location across Massachusetts. 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

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