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NCT06297941 · ClinicalTrials.gov registry record · Phase 1

Study of REM-422 in Patients With AML or Higher Risk MDS

A Phase 1 study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, sponsored by Remix Therapeutics.

Recruiting
Registry status
Phase 1
Development phase
100
Enrollment target
9
Study locations

NCT06297941 is a Phase 1 study of Acute Myeloid Leukemia and Myelodysplastic Syndromes that is actively recruiting participants, run by Remix Therapeutics. The registered enrollment target is 100 participants, below the 116-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (14% lower). The trial reports 9 study locations across 6 states.

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The verdict

NCT06297941, a Phase 1 study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, is actively recruiting participants, sponsored by Remix Therapeutics.

RECRUITING
Registry status
Phase 1
Development phase
100 participants
Enrollment target
9
Study locations

Study Summary

The goal of this study is to determine the safety and antitumor effects of REM-422, a MYB mRNA degrader, in people with Higher Risk MDS and relapsed/refractory AML

Interventions

  • DRUG REM-422

Study Locations (9)

Other

  • Centre Hospitalier Universitaire (CHU) de Bordeaux - Bordeaux
  • AP-HP - Hôpital Saint-Louis - Paris
  • IUCT-Oncopole - Toulouse
  • Institut de Cancerologie Gustave-Roussy - Villejuif

California

  • City of Hope - Duarte

Florida

  • Moffitt Cancer Center - Tampa

Massachusetts

  • Massachusetts General Hospital - Boston

New York

  • Memorial Sloan Kettering - New York

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2024-04-26
Est. Completion 2027-06-15
Phase Phase 1

Sponsor

Remix Therapeutics

2 total trials

What the Registry Record Tells You About NCT06297941

The ClinicalTrials.gov registry entry for NCT06297941 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 116-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (14% lower). The listed sponsor is Remix Therapeutics, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Acute Myeloid Leukemia appearing as the primary indexed condition, and to 1 intervention - of which REM-422 is the first listed.

NCT06297941 reports 9 study locations spanning 6 distinct geographic areas - top geographies include Other, California, Florida.

Frequently Asked Questions

What is clinical trial NCT06297941 about?

NCT06297941 is a clinical study titled "Study of REM-422 in Patients With AML or Higher Risk MDS". The goal of this study is to determine the safety and antitumor effects of REM-422, a MYB mRNA degrader, in people with Higher Risk MDS and relapsed/refractory AML

What is the current status of trial NCT06297941?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 100 participants. The study started on 2024-04-26. Estimated completion is 2027-06-15.

What conditions does trial NCT06297941 study?

This clinical trial studies the following conditions: Acute Myeloid Leukemia, Myelodysplastic Syndromes, Acute Myeloid Leukemia Refractory, Higher-risk Myelodysplastic Syndromes.

What interventions are being tested in trial NCT06297941?

The interventions under investigation include: REM-422 (DRUG).

Who is sponsoring clinical trial NCT06297941?

This trial is sponsored by Remix Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06297941 being conducted?

This trial has 9 study locations across California, Florida, Massachusetts, New York, 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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