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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00161668
Other study ID # 0903X-100847
Secondary ID
Status Completed
Phase Phase 4
First received September 8, 2005
Last updated March 14, 2007
Start date October 2001

Study information

Verified date March 2007
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study is designed to assess the safety of Mylotarg therapy in routine practice.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Treated by Mylotarg

- Provide ICF

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Intervention

Drug:
Mylotarg


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wyeth is now a wholly owned subsidiary of Pfizer

Country where clinical trial is conducted

United States, 

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