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NCT06472661 · ClinicalTrials.gov registry record · Early Phase 1

FUSA With Intratumoral PolyICLC in Regionally Advanced Resectable Melanoma

A Early Phase 1 study of Advanced Melanoma, sponsored by University of Virginia.

Recruiting
Registry status
Early Phase 1
Development phase
11
Enrollment target
1
Study location

NCT06472661 is a Early Phase 1 study of Advanced Melanoma that is actively recruiting participants, run by University of Virginia. The registered enrollment target is 11 participants, below the 171-participant average among 21 other Advanced Melanoma trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06472661, a Early Phase 1 study of Advanced Melanoma, is actively recruiting participants, sponsored by University of Virginia.

RECRUITING
Registry status
Early Phase 1
Development phase
11 participants
Enrollment target
1
Study location

Study Summary

This study is for adult patients with advanced melanoma who are receiving immunotherapy and who are planning on having surgery for their cancer. All participants in this study will receive an experimental treatment made up of focused ultrasound ablation (FUSA), a non-invasive experimental treatment that uses ultrasound waves to heat and destroy tumor tissue, and an injection in the tumor with an experimental drug that activates the immune system called polyICLC (polyinosinic-polycytidylic acid that is stabilized with carboxymethylcellulose and polylysine). Neither the drug nor the device that are used in this study have been approved by the U.S. Food and Drug Administration (FDA).

Conditions Studied

Interventions

  • DEVICE Echopulse or Echopulse HD
  • DRUG PolyICLC

Study Locations (1)

Virginia

  • University of Virginia - Charlottesville

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2024-09-27
Est. Completion 2026-08
Phase Early Phase 1

Sponsor

University of Virginia

449 total trials

What the Registry Record Tells You About NCT06472661

The ClinicalTrials.gov registry entry for NCT06472661 describes a study currently listed as recruiting, categorized as Early Phase 1. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 171-participant average among 21 other Advanced Melanoma trials with a reported enrollment target (94% lower). The listed sponsor is University of Virginia, which has 449 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Advanced Melanoma appearing as the primary indexed condition, and to 2 interventions - of which Echopulse or Echopulse HD is the first listed.

NCT06472661 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.

Frequently Asked Questions

What is clinical trial NCT06472661 about?

NCT06472661 is a clinical study titled "FUSA With Intratumoral PolyICLC in Regionally Advanced Resectable Melanoma". This study is for adult patients with advanced melanoma who are receiving immunotherapy and who are planning on having surgery for their cancer. All participants in this study will receive an experimental treatment made up of focused ultrasound ablation (FUSA), a non-invasive experimental treatment ...

What is the current status of trial NCT06472661?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 11 participants. The study started on 2024-09-27. Estimated completion is 2026-08.

What conditions does trial NCT06472661 study?

This clinical trial studies the following conditions: Advanced Melanoma.

What interventions are being tested in trial NCT06472661?

The interventions under investigation include: Echopulse or Echopulse HD (DEVICE), PolyICLC (DRUG).

Who is sponsoring clinical trial NCT06472661?

This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06472661 being conducted?

This trial has 1 study location across Virginia. 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.