Baloxavir Versus Oseltamivir for Nursing Home Influenza Outbreaks
Primary Purpose
Influenza, Influenza, Human, Influenza -Like Illness
Status
Active
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Oseltamivir
Baloxavir
Sponsored by
About this trial
This is an interventional prevention trial for Influenza focused on measuring Antiviral Medication, Influenza, Nursing Home, Influenza Outbreak, Outbreak, Oseltamivir, Baloxavir
Eligibility Criteria
Inclusion Criteria:
- Medicare-certified NHs in any location in the United States with at least 50 long-stay residents 18 years of age or older.
- Facilities with at least 80% of their long-stay population 65 years of age or older
Exclusion Criteria:
- Hospital-based facilities
- Facilities not submitting MDS data
Sites / Locations
- Insight Therapeutics, LLC
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Oseltamivir
Baloxavir
Arm Description
Nursing homes randomized to receive oseltamivir for treatment and chemoprophylaxis for influenza.
Nursing homes randomized to receive baloxavir for treatment and chemoprophylaxis for influenza.
Outcomes
Primary Outcome Measures
Total number of ILI cases defined, following the index influenza case identification in nursing homes randomized to baloxavir or oseltamivir
To demonstrate the non-inferiority of prophylactic baloxavir vs. oseltamivir to prevent influenza-like illness (ILI) after an index influenza case in nursing homes.
Secondary Outcome Measures
Outbreak duration defined as the time of the first laboratory-confirmed case of influenza to 7 days following the last identified case of influenza-like illness requiring treatment with baloxavir or oseltamivir
To determine the difference in total outbreak duration for each outbreak occurring in nursing homes randomized to offer either single-dose baloxavir or oseltamivir for outbreak abatement during the 2021-2022 influenza season.
Facility-level data on antiviral courses of treatment administered from Medication Administration Records
To determine the difference in number of courses of treatment of baloxavir or oseltamivir needed for outbreak control in nursing homes randomized to baloxavir or oseltamivir.
Hospitalizations from Minimum Data Set (MDS) 3.0 (interim) and Medicare A claims
To determine the difference in respiratory-related hospitalization rates during the 2021-2022 influenza season experienced by long-stay nursing home residents 65 and older living in nursing homes randomized to either baloxavir or oseltamivir.
Mortality from Medicare Vital Status File
To determine the differences in long-stay residents' mortality rates in nursing homes randomized to either baloxavir or oseltamivir.
Full Information
NCT ID
NCT05012189
First Posted
August 12, 2021
Last Updated
March 14, 2023
Sponsor
Insight Therapeutics, LLC
Collaborators
Brown University, Case Western Reserve University, Genentech, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT05012189
Brief Title
Baloxavir Versus Oseltamivir for Nursing Home Influenza Outbreaks
Official Title
Comparative Effectiveness of Baloxavir Versus Oseltamivir for Influenza Outbreak Management in U.S. Nursing Homes
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 6, 2021 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insight Therapeutics, LLC
Collaborators
Brown University, Case Western Reserve University, Genentech, Inc.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Influenza outbreaks are a prevalent event in nursing homes (NHs). We will study baloxavir compared to oseltamivir when used for influenza prophylaxis when facilities identify an index incident case of influenza. This study will help guide nursing home's decision making and demonstrate the effectiveness of a novel antiviral for preventing influenza outbreaks.
Detailed Description
A random study sample of about 1000 U.S. nursing homes (NHs), housing approximately 112,000 overall residents and 92,000 over the age of 65 years, of whom 64,500 are long-stay NH residents, will be recruited for the study. Participating facilities will be randomly allocated in a 1:1 ratio to oseltamivir or baloxavir for antiviral treatment and prophylaxis. Primary study data provided by facilities monthly during the influenza season will support primary and secondary endpoints along with administrative claims and public use datasets containing information on facility characteristics.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza, Influenza, Human, Influenza -Like Illness
Keywords
Antiviral Medication, Influenza, Nursing Home, Influenza Outbreak, Outbreak, Oseltamivir, Baloxavir
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Pragmatic Cluster Randomized Clinical Trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1000 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Oseltamivir
Arm Type
Active Comparator
Arm Description
Nursing homes randomized to receive oseltamivir for treatment and chemoprophylaxis for influenza.
Arm Title
Baloxavir
Arm Type
Experimental
Arm Description
Nursing homes randomized to receive baloxavir for treatment and chemoprophylaxis for influenza.
Intervention Type
Drug
Intervention Name(s)
Oseltamivir
Intervention Description
Nursing home residents and staff 18 years and older are allocated to receive oseltamivir for treatment and chemoprophylaxis for influenza.
Intervention Type
Drug
Intervention Name(s)
Baloxavir
Intervention Description
Nursing home residents and staff 18 years and older are allocated to receive baloxavir for treatment and chemoprophylaxis for influenza.
Primary Outcome Measure Information:
Title
Total number of ILI cases defined, following the index influenza case identification in nursing homes randomized to baloxavir or oseltamivir
Description
To demonstrate the non-inferiority of prophylactic baloxavir vs. oseltamivir to prevent influenza-like illness (ILI) after an index influenza case in nursing homes.
Time Frame
Up to 8 months each influenza season
Secondary Outcome Measure Information:
Title
Outbreak duration defined as the time of the first laboratory-confirmed case of influenza to 7 days following the last identified case of influenza-like illness requiring treatment with baloxavir or oseltamivir
Description
To determine the difference in total outbreak duration for each outbreak occurring in nursing homes randomized to offer either single-dose baloxavir or oseltamivir for outbreak abatement during the 2021-2022 influenza season.
Time Frame
Up to 8 months each influenza season
Title
Facility-level data on antiviral courses of treatment administered from Medication Administration Records
Description
To determine the difference in number of courses of treatment of baloxavir or oseltamivir needed for outbreak control in nursing homes randomized to baloxavir or oseltamivir.
Time Frame
Up to 8 months each influenza season
Title
Hospitalizations from Minimum Data Set (MDS) 3.0 (interim) and Medicare A claims
Description
To determine the difference in respiratory-related hospitalization rates during the 2021-2022 influenza season experienced by long-stay nursing home residents 65 and older living in nursing homes randomized to either baloxavir or oseltamivir.
Time Frame
Up to 8 months each influenza season
Title
Mortality from Medicare Vital Status File
Description
To determine the differences in long-stay residents' mortality rates in nursing homes randomized to either baloxavir or oseltamivir.
Time Frame
Up to 8 months each influenza season
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
120 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
- Medicare-certified NHs in any location in the United States with at least 50 long-stay residents 18 years of age or older.
Exclusion Criteria:
Hospital-based facilities
Facilities not submitting MDS data
Facility Information:
Facility Name
Insight Therapeutics, LLC
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23510
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Baloxavir Versus Oseltamivir for Nursing Home Influenza Outbreaks
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