The disappointing benefit seen in Pfizer Inc.’s clinical study of Paxlovid (nirmatrelvir and ritonavir) in standard-risk COVID-19 patients suggests that even if the drug was authorized or approved for patients at standard risk as well as those at high risk of hospitalization and death, the oral antiviral is unlikely to get much uptake in the lower-risk population.
Pfizer’s Paxlovid Likely Relegated To High-Risk COVID-19 Patients
The company announced updated results from a standard-risk study, which it will include in its overall new drug application, but whether Paxlovid will see approval or uptake in that group is another question.
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