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ACTIVE NOT RECRUITING Phase 1

Safety and Efficacy of IMC-F106C as a Single Agent and in Combination With Checkpoint Inhibitors

NCT04262466 · View on ClinicalTrials.gov ↗

Study Summary

Brenetafusp (IMC-F106C) is an immune-mobilizing monoclonal T cell receptor against cancer (ImmTAC ®) designed for the treatment of cancers positive for the tumor-associated antigen PRAME. This is a first-in-human trial designed to evaluate the safety and efficacy of brenetafusp in adult participants who have the appropriate HLA-A2 tissue marker and whose cancer is positive for PRAME.

Interventions

  • DRUG Brenetafusp
  • DRUG Brenetafusp and pembrolizumab
  • DRUG Brenetafusp and chemotherapy
  • DRUG Brenetafusp and monoclonal antibodies and chemotherapy
  • DRUG Brenetafusp and tebentafusp

Study Locations (20)

California

  • University of California - San Diego — La Jolla
  • Angeles Clinic and Research Institute — Los Angeles
  • University of California Davis Comprehensive Center — Sacramento

Pennsylvania

  • Abramson Cancer Center of the University of Pennsylvania — Philadelphia
  • Thomas Jefferson University Hospital — Philadelphia
  • UPMC Hillman Cancer Center — Pittsburgh

New York

  • Columbia University Medical Center — New York
  • Memorial Sloan Kettering — New York

Colorado

  • University of Colorado — Aurora

District of Columbia

  • Georgetown University Medical Center — Washington D.C.

Florida

  • Houston Lee Moffitt Cancer Center & Research Institute — Tampa

Illinois

  • The University of Chicago Medical Center — Chicago

Iowa

  • University of Iowa — Iowa City

Trial Details

FieldValue
Enrollment Target 410 participants
Start Date 2020-02-25
Est. Completion 2027-12
Phase Phase 1

Sponsor

Immunocore

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04262466

The ClinicalTrials.gov registry entry for NCT04262466 describes a study currently listed as active not 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 410 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Immunocore, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Select Advanced Solid Tumors appearing as the primary indexed condition, and to 5 interventions — of which Brenetafusp 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: NCT04262466 reports 20 study locations spanning 15 distinct geographic areas — top geographies include California, Pennsylvania, New York. 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 NCT04262466 about?

NCT04262466 is a clinical study titled "Safety and Efficacy of IMC-F106C as a Single Agent and in Combination With Checkpoint Inhibitors". Brenetafusp (IMC-F106C) is an immune-mobilizing monoclonal T cell receptor against cancer (ImmTAC ®) designed for the treatment of cancers positive for the tumor-associated antigen PRAME. This is a first-in-human trial designed to evaluate the safety and efficacy of brenetafusp in adult participants...

What is the current status of trial NCT04262466?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 410 participants. The study started on 2020-02-25. Estimated completion is 2027-12.

What conditions does trial NCT04262466 study?

This clinical trial studies the following conditions: Select Advanced Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04262466?

The interventions under investigation include: Brenetafusp (DRUG), Brenetafusp and pembrolizumab (DRUG), Brenetafusp and chemotherapy (DRUG), Brenetafusp and monoclonal antibodies and chemotherapy (DRUG), Brenetafusp and tebentafusp (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04262466?

This trial is sponsored by Immunocore, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04262466 being conducted?

This trial has 20 study locations across California, Colorado, District of Columbia, Florida, Illinois. 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