ClinicalTrials.gov record
Completed Phase 1Phase 2 Interventional Results available

Dose Escalation Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics of ASP2215 in Patients With Relapsed or Refractory Acute Myeloid Leukemia

ClinicalTrials.gov ID: NCT02014558

Public ClinicalTrials.gov record NCT02014558. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 12, 2026, 8:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Open-Label, Dose Escalation Study Investigating the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ASP2215 in Patients With Relapsed or Refractory Acute Myeloid Leukemia

Study identification

NCT ID
NCT02014558
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Astellas Pharma Global Development, Inc.
Industry
Enrollment
265 participants

Conditions and interventions

Interventions

  • Cephalexin Drug
  • Gilteritinib Drug
  • Midazolam Drug
  • Voriconazole Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 8, 2013
Primary completion
Aug 3, 2017
Completion
Mar 6, 2018
Last update posted
Dec 2, 2024

2013 – 2018

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Site US10021 Birmingham Alabama 35294
Site US10023 Scottsdale Arizona 85259
Site US10022 Duarte California 91010
Site US10008 Los Angeles California 90095-1678
Site US10005 San Francisco California 94143
Site US10001 Chicago Illinois 60611
Site US10015 Chicago Illinois 60637
Site US10012 Baltimore Maryland 21201
Site US10003 Baltimore Maryland 21287
Site US10006 Minneapolis Minnesota 55455
Site US10011 Rochester Minnesota 55905
Site US10020 Hackensack New Jersey 07601
Site US10010 Buffalo New York 14263
Site US10009 New York New York 10022
Site US10013 New York New York 10032
Site US10019 New York New York 10065
Site US10014 Cleveland Ohio 44195
Site US10018 Hershey Pennsylvania 17033
Site US10004 Philadelphia Pennsylvania 19104
Site US10017 Charleston South Carolina 29425-8900
Site US10007 Nashville Tennessee 37232
Site US10002 Houston Texas 77030
Site US10026 Fairfax Virginia 22031

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02014558, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 2, 2024 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02014558 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →