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Pfizer starts Phase 2/3 clinical study to evaluate safety, efficacy of COVID-19 oral treatment in pediatric population

By ANI | Updated: March 9, 2022 19:05 IST

Pharmaceutical company Pfizer on Tuesday (local time) stated that it has started the Phase 2/3 clinical study to evaluate the safety and efficacy of its COVID-19 oral treatment in the pediatric population at risk of progression to severe disease.

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Pharmaceutical company Pfizer on Tuesday (local time) stated that it has started the Phase 2/3 clinical study to evaluate the safety and efficacy of its COVID-19 oral treatment in the pediatric population at risk of progression to severe disease.

"Today, we announced the start of a Phase 2/3 study to evaluate the safety and efficacy of our COVID-19 oral treatment in pediatric participants at risk of progression to severe disease. We are eager to address the need for treatment in this important population," it said in a tweet.

The pharmaceutical company further said Pfizer's oral treatment is not approved but is authorized for emergency use by the Food and Drug Administration (FDA) to treat mild-to-moderate COVID-19 in high-risk patients 12 plus, weighing at least 40 kg, with positive results of SARS-CoV-2 viral testing.

( With inputs from ANI )

Disclaimer: This post has been auto-published from an agency feed without any modifications to the text and has not been reviewed by an editor

Tags: Food And Drug AdministrationFood products, medicinesUnited states food and drug administrationCommissioner of food and drugs administrationPfizerUsfdaUnited states' food and drug administrationUnited states food & drug administrationU.s. food and drug administration
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