COVID-19
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who meet all of the following criteria are eligible for this study. 1) Patients who received ensitrelvir between November 2022 and April 2023 2) Patients who received ensitrelvir according to the package insert 3) Patients who have all the following required data (1)Start date and end date of ensitrelvir administration (2)SARS-CoV-2 positive test result (3)Clinical symptoms after starting administration of ensitrelvir (4)Outcomes of SARS-CoV-2 infection
Exclusion criteria
Exclusion criteria: Patients who meet any of the following criteria are excluded from the study. 1) Patients who were treated off-label 2) Patients who refuse to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical symptoms, oxygen saturation, and food amount at each time point from the start to Day 10 of ensitrelvir administration. | — |
Secondary
| Measure | Time frame |
|---|---|
| Outcomes of SARS-CoV-2 infection up to 10 days after the end of administration | — |
Countries
Japan
Contacts
Shionogi & Co., Ltd. Medical Affairs