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NCT03988205 · ClinicalTrials.gov registry record · Phase 4

Patients Receiving Induction With Liposomal Daunorubicin and Cytarabine (CPX-351) for Acute Myeloid Leukemia

A Phase 4 study, sponsored by Medical College of Wisconsin.

Terminated
Registry status
Phase 4
Development phase
3
Enrollment target

NCT03988205 is a Phase 4 study that was terminated before completion, run by Medical College of Wisconsin. The registered enrollment target is 3 participants.

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The verdict

NCT03988205, a Phase 4 study, was terminated before completion, sponsored by Medical College of Wisconsin.

TERMINATED
Registry status
Phase 4
Development phase
3 participants
Enrollment target

Study Summary

This is a single-arm, single-site run-in phase (six subjects) followed by a multicenter continuation phase (114 subjects), Phase IV study. Eligible subjects will be receiving CPX-351 as their usual medical care administered according to FDA approval, as a condition for participation.

Interventions

  • DRUG CPX-351
  • BEHAVIORAL Outpatient Care Model

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2019-08-28
Est. Completion 2022-04-01
Phase Phase 4

Sponsor

Medical College of Wisconsin

447 total trials

What the Registry Record Tells You About NCT03988205

The ClinicalTrials.gov registry entry for NCT03988205 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 3 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical College of Wisconsin, which has 447 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which CPX-351 is the first listed.

NCT03988205 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03988205 about?

NCT03988205 is a clinical study titled "Patients Receiving Induction With Liposomal Daunorubicin and Cytarabine (CPX-351) for Acute Myeloid Leukemia". This is a single-arm, single-site run-in phase (six subjects) followed by a multicenter continuation phase (114 subjects), Phase IV study. Eligible subjects will be receiving CPX-351 as their usual medical care administered according to FDA approval, as a condition for participation.

What is the current status of trial NCT03988205?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 3 participants. The study started on 2019-08-28. Estimated completion is 2022-04-01.

What interventions are being tested in trial NCT03988205?

The interventions under investigation include: CPX-351 (DRUG), Outpatient Care Model (BEHAVIORAL).

Who is sponsoring clinical trial NCT03988205?

This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.

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.