Individual Patient Expanded Access Gilteritinib (ASP2215)

NCT03315299 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2024-02-07

No results posted yet for this study

Summary

The purpose of this study is to provide expanded access to ASP2215 for a single subject with refractory FLT3-mutated AML without access to comparable or alternative therapy.

Conditions

Interventions

DRUG

ASP2215

Subject will take ASP2215 by mouth daily for 28 day cycles

Sponsors & Collaborators

  • Astellas Pharma Global Development, Inc.

    collaborator INDUSTRY
  • Etan Orgel

    lead OTHER

Eligibility

Min Age
12 Years
Max Age
15 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03315299 on ClinicalTrials.gov