The Chinese Centre for Disease Control and Prevention (CDC) has said that COVID-19 vaccines being developed in China may be ready for use by the general public as early as November 2020, Reuters news agency reported on Tuesday.
Currently, China has four COVID-19 vaccines in the final stage of clinical trials. At least three of those have already been offered to essential workers under an emergency use programme launched in July 2020.
CDC chief biosafety expert, Guizhen Wu, was quoted as saying in an interview with state TV that Phase 3 clinical trials were proceeding smoothly and the vaccines could be ready for the general public in November or December 2020.
Wu, who said she has experienced no abnormal symptoms in recent months after taking an experimental vaccine herself in April 2020, did not specify which vaccines she was referring to.
Reportedly, a unit of state pharmaceutical giant China National Pharmaceutical Group (Sinopharm) and the US-listed Sinovac Biotech (Nasdaq:SVA) are developing the three vaccines under the state's emergency use programme. A fourth COVID-19 vaccine being developed by CanSino Biologics (HKSE:6185.HK) was approved for use by the Chinese military in June 2020.
Also, Sinopharm had said in July 2020 that its vaccine could be ready for public use by the end of this year after the conclusion of Phase 3 trials.
Genentech reports positive Phase II results for enicepatide in type 2 diabetes
Pharming reports positive Phase II data for leniolisib in primary immunodeficiencies
Insmed's ARIKAYCE sNDA granted priority review by FDA
Precigen announces FDA platform technology designation for AdenoVerse
Enhertu recommended for EU approval in early HER2-positive breast cancer
PureTech receives FDA Fast Track designation for LYT-200 in HR-MDS
CHMP recommends EU approval of Klygefa for generalised myasthenia gravis
Coiled Therapeutics completes enrolment in two AO-252 formulation cohorts
MaaT Pharma outlines potential Phase 3 development plan for MaaT013 after CHMP negative opinion
Kemp Proteins partners with NeuImmune to advance precision protein production
Bayer's Kerendia wins FDA approval for chronic kidney disease associated with type 1 diabetes