Sinovac applies for EUA in PH amid incomplete submission

Chinese pharmaceutical company Sinovac has submitted an application for emergency use authorization (EUA) to the Philippine Food and Drug Administration (FDA).

FDA Director General Eric Domingo stated that Sinovac has not yet completed the submission of all necessary requirements for an EUA.

Specifically, the company has only submitted Phase 1 and Phase 2 clinical trial results, and Phase 3 human trial results are still needed to assess the vaccine's benefits and risks.

The efficacy of Sinovac's vaccine has varied in different trial locations, showing 50% in Brazil, 65% in Indonesia, and 91% in Turkey.

The Philippines aims to secure 25 million doses of the Sinovac vaccine in the first quarter of the year.

Sinovac has already received EUA in China and Indonesia.

Topics in this story

Explore more stories about these topics.

🤖

This story was generated by AI to help you understand the key points. For more detailed coverage, please see the news articles from trusted media outlets below.