The Philippine Vaccine Expert Panel (VEP), chaired by the Department of Science and Technology, has cleared China's Sinovac COVID-19 vaccine for Phase 3 clinical trials in the country.
However, Sinovac must still receive approval from the Philippines' Ethics Board Committee before it can apply to the Food and Drug Administration (FDA) for clinical trials.
The VEP reviews Phase 1 and 2 clinical trials, while the Ethics Board evaluates participant selection and other safeguards.
FDA Director General Rolando Enrique Domingo stated that Sinovac secured the VEP's clearance on Monday.
If Sinovac secures Ethics Board approval, the FDA's evaluation for its clinical trial application is expected to take 14 to 21 days.
🤖
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.
News Sources
See how different news organizations are covering this story. Below are the original articles from various Philippine news sources that contributed to this summary.




