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NCT06660420 · ClinicalTrials.gov registry record · Phase 1

Phase 1 Dose Escalation and Expansion Study of PRAME T Cell Receptor (TCR) Engineered NK Cells in Participants With Recurrent and/or Refractory Melanoma (PRAMETIME-Mel)

A Phase 1 study of Recurrent Melanoma and Refractory Melanoma, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
Phase 1
Development phase
39
Enrollment target
1
Study location

NCT06660420 is a Phase 1 study of Recurrent Melanoma and Refractory Melanoma that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 39 participants, below the 171-participant average among 23 other Recurrent Melanoma trials with a reported enrollment target (77% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06660420, a Phase 1 study of Recurrent Melanoma and Refractory Melanoma, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

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

Study Summary

To find the highest tolerable dose and recommended dose of PRAME-TCR-NK cells that can be given to participants with recurrent and/or refractory melanoma. The safety and tolerability of PRAME-TCR-NK cells will also be studied.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine

Study Locations (1)

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2025-02-25
Est. Completion 2031-12-31
Phase Phase 1

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT06660420

The ClinicalTrials.gov registry entry for NCT06660420 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 39 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 171-participant average among 23 other Recurrent Melanoma trials with a reported enrollment target (77% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Recurrent Melanoma appearing as the primary indexed condition, and to 2 interventions - of which Cyclophosphamide is the first listed.

NCT06660420 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06660420 about?

NCT06660420 is a clinical study titled "Phase 1 Dose Escalation and Expansion Study of PRAME T Cell Receptor (TCR) Engineered NK Cells in Participants With Recurrent and/or Refractory Melanoma (PRAMETIME-Mel)". To find the highest tolerable dose and recommended dose of PRAME-TCR-NK cells that can be given to participants with recurrent and/or refractory melanoma. The safety and tolerability of PRAME-TCR-NK cells will also be studied.

What is the current status of trial NCT06660420?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2025-02-25. Estimated completion is 2031-12-31.

What conditions does trial NCT06660420 study?

This clinical trial studies the following conditions: Recurrent Melanoma, Refractory Melanoma, Phase 1.

What interventions are being tested in trial NCT06660420?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG).

Who is sponsoring clinical trial NCT06660420?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06660420 being conducted?

This trial has 1 study location across 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

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