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Use of Micafungin (Mycamine®) as Antifungal Prophylaxis in Haematology and Onco-haematology (OLYMPE)

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Astellas

Status

Completed

Conditions

Haemopathy
Antifungal Prophylaxis

Treatments

Drug: Micafungin

Study type

Observational

Funder types

Industry

Identifiers

NCT02127788
FR-MYC-NI-003

Details and patient eligibility

About

The purpose of this observational study is to describe the actual conditions of prescription of micafungin in antifungal prophylaxis in French haematological and onco-haematological units. The efficacy and the safety outcomes will be described.

Enrollment

150 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patient with haemopathy or paediatric patients with haemopathy or solid tumor.
  • Patient hospitalized in haematology, onco-haematology or onco-paediatrics unit.
  • Patient initiating antifungal prophylaxis with micafungin.

Exclusion criteria

  • Patient presenting documented fungal infection.
  • Patient already included in a biomedical study impacting the care management of invasive fungal infection at the time of inclusion.

Trial design

150 participants in 1 patient group

Micafungin
Description:
Patients affected with haemopathy (or affected with solid tumor for paediatric patients) under antifungal prophylaxis with micafungin.
Treatment:
Drug: Micafungin

Trial contacts and locations

17

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Data sourced from clinicaltrials.gov

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