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NCT01184898 · ClinicalTrials.gov registry record · NA

Pilot Trial of Sirolimus/MEC in High Risk Acute Myelogenous Leukemia (AML)

A NA study, sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University.

Completed
Registry status
NA
Development phase
36
Enrollment target

NCT01184898: Completed NA study, sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University.

NCT01184898 is a NA study that has completed, run by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University. The registered enrollment target is 36 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01184898, a NA study, has completed, sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University.

COMPLETED
Registry status
NA
Development phase
36 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the addition of Sirolimus (rapamycin) to standard chemotherapy for the treatment of patients with high risk acute myelogenous leukemia (AML). Cancer cells taken from the patients will be studied in the laboratory to see if rapamycin is affecting the mTOR pathway in the cells and if this effect is correlated with how well patients respond to the therapy.

Primary Outcome

Percent change compared between response groups (responder vs nonresponder). This outcome measure only includes patients who survived to outcome assessment.

Interventions

  • DRUG Sirolimus
  • DRUG Etoposide
  • DRUG Cytarabine
  • DRUG Mitoxantrone

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2010-07
Est. Completion 2016-02
Phase NA

What the finished NCT01184898 record still lists

NCT01184898 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 4 interventions - of which Sirolimus is the first listed.

NCT01184898 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01184898 about?

NCT01184898 is a clinical study titled "Pilot Trial of Sirolimus/MEC in High Risk Acute Myelogenous Leukemia (AML)". The purpose of this study is to evaluate the addition of Sirolimus (rapamycin) to standard chemotherapy for the treatment of patients with high risk acute myelogenous leukemia (AML). Cancer cells taken from the patients will be studied in the laboratory to see if rapamycin is affecting the mTOR path...

What is the current status of trial NCT01184898?

This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2010-07. Estimated completion is 2016-02.

What interventions are being tested in trial NCT01184898?

The interventions under investigation include: Sirolimus (DRUG), Etoposide (DRUG), Cytarabine (DRUG), Mitoxantrone (DRUG).

Who is sponsoring clinical trial NCT01184898?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University, which has 138 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01184898's enrollment target sits among peer trials

36 1541st of 2000 higher than 437 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT01184898, the US trial registry maintained by the National Library of Medicine. NCT01184898 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.