Study of FK463 in the Treatment of Candidemia or Invasive Candidiasis

NCT00036179 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2018-01-10

No results posted yet for this study

Summary

The purpose of the study is to evaluate the safety and efficacy of FK463 in the treatment of patients with confirmed candidemia or invasive candidiasis.

Conditions

  • Candidiasis

Interventions

DRUG

FK463

Sponsors & Collaborators

  • Astellas Pharma Inc

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1999-02-27
Primary Completion
2002-01-27
Completion
2002-01-27

Countries

  • Austria
  • France
  • Germany
  • Italy
  • Poland
  • Spain
  • Sweden
  • United Kingdom

Study Locations

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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 NCT00036179 on ClinicalTrials.gov