Last updated: 11/07/2018 04:42:57
Special Drug Use Investigation for Relenza (Pediatrics resistance)
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Special Drug Use Investigation for Relenza (Pediatrics resistance)
Trial description: Special Drug Use Investigation for Relenza (Pediatrics resistance)
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Reiko Saito, Kenji Suzuki, Hideyuki Okano, Naomi Hasegawa, Hiroharu Abe, Shogo Inoshiri. Sensitivity to Influenza Virus and Antipyretic Effects of Zanamivir (Relenza®) in Pediatric Patients with Influenza A and B Virus Infection : Use-Result Surveillance Specified for Pediatric Patients over Three Seasons from 2006 to 2009 Year. [ANTIBIOTICS & CHEMOTHERAPY]. 2011;27(12):123-137.
Medical condition
Influenza, Human
Product
zanamivir
Collaborators
Not applicable
Study date(s)
January 2007 to April 2009
Type
Not applicable
Phase
Not applicable
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2009-08-04
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
Participate in clinical trial
Access to clinical trial data by researchers
Visit website