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NCT02159040 · ClinicalTrials.gov registry record · Phase 2

Phase II Study to Evaluate Overall Response in Patients With Higher Risk Myelodysplastic Syndromes (MDS) Treated With Azacitidine With or Without Deferasirox.

A Phase 2 study, sponsored by Novartis Pharmaceuticals.

Terminated
Registry status
Phase 2
Development phase
1
Enrollment target

NCT02159040 is a Phase 2 study that was terminated before completion, run by Novartis Pharmaceuticals. The registered enrollment target is 1 participants.

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The verdict

NCT02159040, a Phase 2 study, was terminated before completion, sponsored by Novartis Pharmaceuticals.

TERMINATED
Registry status
Phase 2
Development phase
1 participants
Enrollment target

Study Summary

The primary objective of the study is to compare the overall response rate (inclusive of complete response, partial response and hematologic improvement) per IWG 2006 criteria in patients with higher risk MDS treated with azacitidine with or without deferasirox achieved over the course of one year. Hematologic improvement must be maintained for at least 8 weeks.

Interventions

  • DRUG Azacitidine
  • DRUG Azacitidine plus Deferasirox

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2014-09-11
Est. Completion 2015-06-26
Phase Phase 2

Sponsor

Novartis Pharmaceuticals

1,375 total trials

What the Registry Record Tells You About NCT02159040

The ClinicalTrials.gov registry entry for NCT02159040 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.

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

NCT02159040 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02159040 about?

NCT02159040 is a clinical study titled "Phase II Study to Evaluate Overall Response in Patients With Higher Risk Myelodysplastic Syndromes (MDS) Treated With Azacitidine With or Without Deferasirox.". The primary objective of the study is to compare the overall response rate (inclusive of complete response, partial response and hematologic improvement) per IWG 2006 criteria in patients with higher risk MDS treated with azacitidine with or without deferasirox achieved over the course of one year. ...

What is the current status of trial NCT02159040?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 1 participants. The study started on 2014-09-11. Estimated completion is 2015-06-26.

What interventions are being tested in trial NCT02159040?

The interventions under investigation include: Azacitidine (DRUG), Azacitidine plus Deferasirox (DRUG).

Who is sponsoring clinical trial NCT02159040?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 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.