Study to Assess the Safety, Pharmacokinetics, and Efficacy of Baloxavir Marboxil in Healthy Pediatric Participants With Influenza-Like Symptoms
Status: | Recruiting |
---|---|
Conditions: | Influenza |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 1 - 12 |
Updated: | 4/3/2019 |
Start Date: | November 20, 2018 |
End Date: | April 2, 2019 |
Contact: | Reference Study ID Number: CP40563 www.roche.com/about_roche/roche_worldwide.htm |
Email: | global-roche-genentech-trials@gene.com |
Phone: | 888-662-6728 (U.S. and Canada) |
A Multicenter, Randomized, Double-Blind, Active (Oseltamivir)-Controlled Study to Assess the Safety, Pharmacokinetics, and Efficacy of Baloxavir Marboxil in Otherwise Healthy Pediatric Patients 1 to <12 Years of Age With Influenza-Like Symptoms
This study will evaluate the safety, pharmacokinetics, and efficacy of baloxavir marboxil
compared with oseltamivir in a single influenza episode in otherwise healthy pediatric
participants (i.e., 1 to <12 years of age) with influenza-like symptoms.
compared with oseltamivir in a single influenza episode in otherwise healthy pediatric
participants (i.e., 1 to <12 years of age) with influenza-like symptoms.
Inclusion Criteria:
- Aged 1 to < 12 years at randomization (Day 1).
- Written informed consent/assent for study participation obtained from participant's
parents or legal guardian, with assent as appropriate by the participant, depending on
the patient's level of understanding
- Participant able to comply with study requirements, depending on the patient's level
of understanding
- Participant with a diagnosis of influenza virus infection confirmed by the presence of
all of the following:
- Fever ≥ 38 degree celsius (tympanic temperature) at screening
- At least one respiratory symptom (either cough or nasal congestion)
- The time interval between the onset of symptoms and screening is ≤ 48 hours
Exclusion Criteria:
- Severe symptoms of influenza virus infection requiring inpatient treatment
- Concurrent infections requiring systemic antiviral therapy at screening
- Require, in the opinion of the investigator, any of the prohibited medication during
the study
- Previous treatment with peramivir, laninamivir, oseltamivir, zanamivir, or amantadine
within 2 weeks prior to screening
- Immunization with a live/attenuated influenza vaccine in the 2 weeks prior to
randomization
- Concomitant treatment with steroids or other immuno-suppressant therapy
- Known HIV infection or other immunosuppressive disorder
- Uncontrolled renal, vascular, neurologic, or metabolic disease (e.g., diabetes,
thyroid disorders, adrenal disease), hepatitis, cirrhosis, or pulmonary disease or
participants with known chronic renal failure.
- Active cancer at any site
- History of organ transplantation
- Known allergy to either study drug (i.e., baloxavir marboxil and oseltamivir) or to
acetaminophen
- Females with child-bearing potential
- Participation in a clinical trial within 4 weeks or five half-lives of exposure to an
investigational drug prior to screening, whichever is longer
We found this trial at
54
sites
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Site Overview Avail Clinical Research is a renowned and experienced clinical research site conducting Phase...
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University of Alabama at Birmingham The University of Alabama at Birmingham (UAB) traces its roots...
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Children's Hospital Colorado At Children's Hospital Colorado, we see more, treat more and heal more...
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Chicago, Illinois 60611
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3800 Reservoir Rd NW
Washington, District of Columbia 20007
Washington, District of Columbia 20007
(202) 687-7695
Georgetown University Medical Center Georgetown University Medical Center is committed to excellence in research, education...
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