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NCT01130662 · ClinicalTrials.gov registry record · Phase 1

Combination of Decitabine and Midostaurin in Patients Older Than 60 With Newly Diagnosed or Relapsed Refractory Acute Myeloid Leukemia

A Phase 1 study, sponsored by University of Kansas.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target

NCT01130662: Completed Phase 1 study, sponsored by University of Kansas.

NCT01130662 is a Phase 1 study that has completed, run by University of Kansas. The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01130662, a Phase 1 study, has completed, sponsored by University of Kansas.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

The purpose of this study is to determine the tolerated dose of the combination of decitabine and midostaurin as induction (first cycle of chemotherapy) and consolidation (additional chemotherapy once a patient goes into remission) in people greater than 60 years with newly diagnosed AML or adult patients with relapsed/refractory disease.

Interventions

  • DRUG combination therapy using decitabine and midostaurin

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2010-03
Est. Completion 2011-10
Phase Phase 1
University of Kansas

66 total trials

What the finished NCT01130662 record still lists

NCT01130662 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).

The record links to 0 conditions, and to 1 intervention - of which combination therapy using decitabine and midostaurin is the first listed.

NCT01130662 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01130662 about?

NCT01130662 is a clinical study titled "Combination of Decitabine and Midostaurin in Patients Older Than 60 With Newly Diagnosed or Relapsed Refractory Acute Myeloid Leukemia". The purpose of this study is to determine the tolerated dose of the combination of decitabine and midostaurin as induction (first cycle of chemotherapy) and consolidation (additional chemotherapy once a patient goes into remission) in people greater than 60 years with newly diagnosed AML or adult pa...

What is the current status of trial NCT01130662?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2010-03. Estimated completion is 2011-10.

What interventions are being tested in trial NCT01130662?

The interventions under investigation include: combination therapy using decitabine and midostaurin (DRUG).

Who is sponsoring clinical trial NCT01130662?

This trial is sponsored by University of Kansas, which has 66 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01130662's enrollment target sits among peer trials

16 1786th of 2000 higher than 203 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01130662, the US trial registry maintained by the National Library of Medicine. NCT01130662 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.