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NCT06383572 · ClinicalTrials.gov registry record · Phase 1

Phase I/II Study of Engineered T Cell Receptor-Modified NK Cells Targeting PRAME in Conjunction With Lymphodepleting Chemotherapy for the Management of Relapse/Refractory Myeloid Malignancies

A Phase 1 study of Myeloid Malignancies and Lymphodepleting Chemotherapy, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
Phase 1
Development phase
44
Enrollment target
1
Study location

NCT06383572 is a Phase 1 study of Myeloid Malignancies and Lymphodepleting Chemotherapy that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 44 participants, roughly in line with the 43-participant average among 5 other Myeloid Malignancies trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT06383572, a Phase 1 study of Myeloid Malignancies and Lymphodepleting Chemotherapy, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

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

Study Summary

To find a recommended dose of PRAME-TCR-NK cells that can be given to patients with AML or MDS.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Decitabine
  • DRUG Fludarabine phosphate
  • DRUG Dexamethasone

Study Locations (1)

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2024-06-26
Est. Completion 2029-04-01
Phase Phase 1

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT06383572

The ClinicalTrials.gov registry entry for NCT06383572 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 43-participant average among 5 other Myeloid Malignancies trials with a reported enrollment target. The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Myeloid Malignancies appearing as the primary indexed condition, and to 4 interventions - of which Cyclophosphamide is the first listed.

NCT06383572 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06383572 about?

NCT06383572 is a clinical study titled "Phase I/II Study of Engineered T Cell Receptor-Modified NK Cells Targeting PRAME in Conjunction With Lymphodepleting Chemotherapy for the Management of Relapse/Refractory Myeloid Malignancies". To find a recommended dose of PRAME-TCR-NK cells that can be given to patients with AML or MDS.

What is the current status of trial NCT06383572?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2024-06-26. Estimated completion is 2029-04-01.

What conditions does trial NCT06383572 study?

This clinical trial studies the following conditions: Myeloid Malignancies, Lymphodepleting Chemotherapy.

What interventions are being tested in trial NCT06383572?

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

Who is sponsoring clinical trial NCT06383572?

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

Where is trial NCT06383572 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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