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NCT05038800 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate MK-0482 for Relapsed/Refractory Acute Myeloid Leukemia (AML) or Chronic Myelomonocytic Leukemia (CMML) (MK-0482-002)

A Phase 1 study, sponsored by Merck Sharp & Dohme.

Terminated
Registry status
Phase 1
Development phase
13
Enrollment target

NCT05038800 is a Phase 1 study that was terminated before completion, run by Merck Sharp & Dohme. The registered enrollment target is 13 participants.

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The verdict

NCT05038800, a Phase 1 study, was terminated before completion, sponsored by Merck Sharp & Dohme.

TERMINATED
Registry status
Phase 1
Development phase
13 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and recommended Phase 2 dose (RP2D) of MK-0482. There are 2 parts of this study. Part 1 is a dose escalation which will follow an accelerated titration design (ATD) for participants with relapsed/refractory (R/R) AML or CMML. Part 2 is a dose expansion for participants with R/R AML.

Interventions

  • BIOLOGICAL MK-0482

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2021-09-26
Est. Completion 2023-12-11
Phase Phase 1

Sponsor

Merck Sharp & Dohme

558 total trials

What the Registry Record Tells You About NCT05038800

The ClinicalTrials.gov registry entry for NCT05038800 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Merck Sharp & Dohme, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which MK-0482 is the first listed.

NCT05038800 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05038800 about?

NCT05038800 is a clinical study titled "A Study to Evaluate MK-0482 for Relapsed/Refractory Acute Myeloid Leukemia (AML) or Chronic Myelomonocytic Leukemia (CMML) (MK-0482-002)". The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and recommended Phase 2 dose (RP2D) of MK-0482. There are 2 parts of this study. Part 1 is a dose escalation which will follow an accelerated titration design (ATD) for participants with relapsed/r...

What is the current status of trial NCT05038800?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 13 participants. The study started on 2021-09-26. Estimated completion is 2023-12-11.

What interventions are being tested in trial NCT05038800?

The interventions under investigation include: MK-0482 (BIOLOGICAL).

Who is sponsoring clinical trial NCT05038800?

This trial is sponsored by Merck Sharp & Dohme, which has 558 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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.