A Study to Investigate the Safety and Efficacy of Fidaxomicin (Oral Suspension or Tablets) and Vancomycin (Oral Liquid or Capsules) in Pediatric Subjects With Clostridium Difficile-associated Diarrhea (CDAD)

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 3, MULTICENTER, INVESTIGATOR-BLIND, RANDOMIZED, PARALLEL GROUP STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF FIDAXOMICIN ORAL SUSPENSION OR TABLETS TAKEN Q12H, AND VANCOMYCIN ORAL LIQUID OR CAPSULES TAKEN Q6H, FOR 10 DAYS IN PEDIATRIC SUBJECTS WITH CLOSTRIDIUM DIFFICILE-ASSOCIATED DIARRHEA. THE SUNSHINE STUDY (VERSION 1.1, 05-JUNE 2014)

Intervention/treatment:
FIDAXOMICIN
Medical condition:
CLOSTRIDIUM DIFFICILE INFECTION
Protocol code:
2819-CL-0202
Control number:
176707
Status:
Closed
Approved:
August 22, 2014
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02218372
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
Birth to 17 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Clinical Trial Disclosure
Organization
Astellas Pharma Global Development, Inc.
Phone:
800-888-7704
Sponsor
ASTELLAS PHARMA EUROPE B.V.

Locations

Ontario

Site CA15003
Oshawa, Ontario, L1G 2B9

Results

See the results from the trial NCT02218372. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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