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OpenTrials
Completed

NCT Number: NCT01315457

Infections Associated With the Use of Alemtuzumab

The aim of this study is to propose infection prophylaxis from Asian multinational retrospective analysis of infectious complications in patients who were treated with alemtuzumab

Completed

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Key information

Age range

15 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Queen Mary Hospital, Hong Kong, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients received alemtuzumab as a treatment for hematologic malignancy ex. non-Hodgkin lymphoma Acute myeloid leukemia Aplastic anemia

Exclusion criteria

  • Patients did not receive alemtuzumab

Treatment and study plan

Primary outcomes

  1. Infectious event

    Time frame: one year

    Any infectious complication occurred within one year after the use of alemtuzumab

Sponsors and collaborators

Lead sponsor

Samsung Medical Center

Other

Collaborators

  • Asan Medical Center
  • Chonbuk National University
  • Chonnam National University
  • Chulalongkorn University
  • Dr Cipto Mangunkusumo General Hospital
  • Kyungpook National University Hospital
  • National Taiwan University Hospital
  • Queen Mary Hospital, Hong Kong
  • Soon Chun Hyang University
  • Yonsei University

Registry information

Official study title

Asian Multinational Retrospective Analysis for Infectious Complications in Patients Treated With Alemtuzumab

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Mar 15, 2011
Registry last updated
May 24, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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