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Clinical trialNCT02103478CompletedPhase 1,PHASE2Interventional

Pharmacokinetic Guided Dose Escalation and Dose Confirmation With Oral Decitabine and Oral Cytidine Deaminase Inhibitor (CDAi) in Patients With Myelodysplastic Syndromes (MDS)

SponsorAstex Pharmaceuticals, Inc.Enrollment130MDSMyelodysplastic Syndrome
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

17 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • University of Alberta Hospital

    Edmonton, Alberta, Canada

  • Princess Margaret Cancer Center

    Toronto, Ontario, Canada

  • Sunnybrook Health Sciences Centre, Odette Cancer Centre

    Toronto, Ontario, Canada

  • Hôpital Maisonneuve-Rosemont

    Montreal, Quebec, Canada

United States
  • Mayo Clinic

    Phoenix, Arizona, United States

  • University of Southern California

    Los Angeles, California, United States

  • University of Chicago

    Chicago, Illinois, United States

  • Horizon Oncology

    Lafayette, Indiana, United States

  • Johns Hopkins

    Baltimore, Maryland, United States

  • Dana Farber Cancer Institute

    Boston, Massachusetts, United States

  • Massachusetts General Hospital

    Boston, Massachusetts, United States

  • John Theurer Cancer Center/ Hackensack University Medical Center

    Hackensack, New Jersey, United States

  • Roswell Park Cancer Institute

    Buffalo, New York, United States

  • Weill Cornell Medical College - New York Presbyterian Hospital

    New York, New York, United States

  • Vanderbilt Ingram Cancer Center

    Nashville, Tennessee, United States

  • M. D. Anderson

    Houston, Texas, United States

  • Medical College of Wisconsin

    Milwaukee, Wisconsin, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
28 Oct 2014
Primary completion
5 Jun 2018
Completion
4 Dec 2019
Last update posted
27 Aug 2024
Registered enrollment
130
Registry id
NCT02103478

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.