Prospective Observational Study of Febrile Neutropenia (FN) and Pegfilgrastim Primary Prophylaxis in Breast Cancer and Non-Hodgkin's Lymphoma Patients Receiving High (>20%) FN-risk Chemotherapy

NCT02178475 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 943

Last updated 2018-07-23

Study results available
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Summary

To estimate the incidence of febrile neutropenia in patients with breast cancer and non-Hodgkin's lymphoma receiving high (\> 20%) FN-risk chemotherapy and pegfilgrastim primary prophylaxis.

Conditions

  • Chemotherapy-induced Febrile Neutropenia

Sponsors & Collaborators

Principal Investigators

  • MD · Amgen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-18
Primary Completion
2016-10-28
Completion
2016-10-28

Countries

  • Austria
  • Belgium
  • Bulgaria
  • Czechia
  • France
  • Germany
  • Greece
  • Poland
  • Romania

Study Locations

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Entities

Companies

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 NCT02178475 on ClinicalTrials.gov