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RECRUITING Phase 1

A Phase 1 Study of IM-1021 in Participants With Advanced Cancer

NCT06823167 · View on ClinicalTrials.gov ↗

Study Summary

IM-1021-101 is a Phase 1 study to determine the safety and effectiveness of IM-1021 in treating participants with advanced cancer.

Interventions

  • BIOLOGICAL IM-1021

Study Locations (10)

Michigan

  • University of Michigan — Ann Arbor
  • START Midwest — Grand Rapids

Texas

  • MD Anderson Cancer Center — Houston
  • NEXT Oncology — Irving

California

  • City Of Hope — Duarte

Connecticut

  • Yale University Medical Center — New Haven

Georgia

  • Emory Winship Cancer Institute — Atlanta

Nebraska

  • University of Nebraska Medical Center — Omaha

Ohio

  • Gabrail Cancer Center — Canton

Tennessee

  • Sarah Cannon Research Institute - Oncology Partners — Nashville

Trial Details

FieldValue
Enrollment Target 117 participants
Start Date 2025-02-26
Est. Completion 2029-02
Phase Phase 1

Sponsor

Immunome

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06823167

The ClinicalTrials.gov registry entry for NCT06823167 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 117 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Immunome, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Hematologic Malignancies appearing as the primary indexed condition, and to 1 intervention — of which IM-1021 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06823167 reports 10 study locations spanning 8 distinct geographic areas — top geographies include Michigan, Texas, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06823167 about?

NCT06823167 is a clinical study titled "A Phase 1 Study of IM-1021 in Participants With Advanced Cancer". IM-1021-101 is a Phase 1 study to determine the safety and effectiveness of IM-1021 in treating participants with advanced cancer.

What is the current status of trial NCT06823167?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 117 participants. The study started on 2025-02-26. Estimated completion is 2029-02.

What conditions does trial NCT06823167 study?

This clinical trial studies the following conditions: Hematologic Malignancies, Solid Malignancies. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06823167?

The interventions under investigation include: IM-1021 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06823167?

This trial is sponsored by Immunome, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06823167 being conducted?

This trial has 10 study locations across California, Connecticut, Georgia, Michigan, Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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