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NCT01668173 · ClinicalTrials.gov registry record · Phase 2

HSP90 Inhibitor, AUY922, in Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera Myelofibrosis (Post-PV MF), Post-Essential Thrombocythemia Myelofibrosis (Post-ET MF), and Refractory PV/ET

A Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

Terminated
Registry status
Phase 2
Development phase
7
Enrollment target

NCT01668173: Clinical Trial Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT01668173 is a Phase 2 study that was terminated before completion, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 7 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01668173, a Phase 2 study, was terminated before completion, sponsored by Memorial Sloan Kettering Cancer Center.

TERMINATED
Registry status
Phase 2
Development phase
7 participants
Enrollment target

Study Summary

The purpose of this study is to test a new drug called AUY922. AUY922 is not FDA-approved. AUY922 is a new kind of drug that attacks a protein called HSP90. HSP90 is found in both normal and cancer cells, but the investigators think it is more important in cancer cells. This study will see if AUY922 helps people with myelofibrosis, essential thrombocythemia and polycythemia vera. This study will also see if AUY922 is safe in people with myelofibrosis, essential thrombocythemia and polycythemia vera. It will find out what effects, good and/or bad, AUY922 has on the patient and the disease. The researchers hope that this study will help them to find better treatments for primary myelofibrosis, essential thrombocythemia and polycythemia vera.

Interventions

  • DRUG AUY922

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2012-08
Est. Completion 2015-05
Phase Phase 2

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT01668173

The ClinicalTrials.gov registry entry for NCT01668173 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which AUY922 is the first listed.

NCT01668173 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01668173 about?

NCT01668173 is a clinical study titled "HSP90 Inhibitor, AUY922, in Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera Myelofibrosis (Post-PV MF), Post-Essential Thrombocythemia Myelofibrosis (Post-ET MF), and Refractory PV/ET". The purpose of this study is to test a new drug called AUY922. AUY922 is not FDA-approved. AUY922 is a new kind of drug that attacks a protein called HSP90. HSP90 is found in both normal and cancer cells, but the investigators think it is more important in cancer cells. This study will see if AUY92...

What is the current status of trial NCT01668173?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 7 participants. The study started on 2012-08. Estimated completion is 2015-05.

What interventions are being tested in trial NCT01668173?

The interventions under investigation include: AUY922 (DRUG).

Who is sponsoring clinical trial NCT01668173?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 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, the data changelog, or report a data error.