The head of Philippines Food and Drugs Administration (FDA), Rolando Enrique Domingo, has said that Chinese biopharmaceutical company Sinovac Biotech (Nasdaq:SVA) may start late-stage trials of its COVID-19 vaccine in the country as early as November 2020, Reuters news agency reported on Thursday.
This follows the clearing of the initial stage of the country's screening process.
The FDA expects to receive Sinovac's formal application for phase three clinical trials within two weeks and regulators will make a decision after their evaluation.
A Sinovac spokesman has confirmed that materials had been provided to the Philippines in the hope of starting Phase 3 trials, but gave no timeframe.
Philippine President, Rodrigo Duterte, repeated on 14 October that he preferred that his country source its COVID-19 vaccines from either China or Russia.
He also said he wanted the entire population vaccinated and has previously said he would not reopen schools until a vaccine was available.
Reportedly, the Philippines is also evaluating COVID-19 vaccines of Russia's Gamaleya Research Institute and Johnson & Johnson's Janssen for late-stage trials and is talking to US pharmaceutical company Pfizer Inc and Moderna Inc as potential suppliers.
The Philippines has 346,536 confirmed COVID-19, the highest in the region, and 6,449 deaths.
Avetra unveils site-centric CRO operating model
Valneva reports positive final Phase 2 results for Lyme disease vaccine VLA15
Lunai Bioworks receives first LOI to license next-generation immune cell therapy
BioNet receives positive opinion from EMA for VacPertagen marketing authorisation in EU
Anixa Biosciences secures U.S. Patent strengthening breast cancer vaccine IP into mid 2040s
PharmaJet® and EVA Pharma Partner to Scale Needle-free Polio Immunisation Across Egypt
Frontier IP portfolio company achieves breakthrough in livestock vaccine trials
GC Biopharma's Phase 2 clinical trial results for BARYTHRAX published in Vaccine
Bavarian Nordic secures new EU contract for up to 8 million smallpox and mpox vaccine doses
Zoetis announces EU approval for Portela to relieve osteoarthritis pain in cats
4basebio synthetic DNA used in Phase I/II mRNA therapy trial
Arcturus reports interim Phase 2 data for ARCT-032 in cystic fibrosis
Sanofi reports data showing high-dose flu vaccine delivers superior protection for older adults