Sinovac Biotech ((SVA)) announced an update on their ongoing clinical study.
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Sinovac Biotech is conducting a Phase III clinical trial titled ‘Immunogenicity and Safety of a Rabies Vaccine (Serum-free Vero Cell), Freeze-dried in Comparison With Verorab®, in a Pre-exposure Prophylaxis Regimen in Healthy Populations Aged ≥1 Years.’ The study aims to demonstrate that the Sinovac rabies vaccine is non-inferior to the existing Verorab® vaccine in terms of immunogenicity and safety for pre-exposure prophylaxis in both pediatric and adult populations.
The intervention being tested is a serum-free Vero cell rabies vaccine developed by Sinovac, administered in a freeze-dried form. This vaccine is intended to provide pre-exposure prophylaxis against rabies, a critical preventive measure for those at risk of exposure.
The study employs a randomized, double-blind, active-controlled design with a parallel intervention model. It involves quadruple masking, meaning that participants, care providers, investigators, and outcomes assessors are all blinded to the treatment allocation. The primary purpose of the study is prevention.
The study is set to begin on May 27, 2025, with its primary completion and estimated overall completion dates yet to be announced. The latest update was submitted on June 27, 2025, indicating that the study is not yet recruiting participants.
This update could influence Sinovac’s stock performance and investor sentiment positively, as successful results could position Sinovac’s vaccine as a competitive alternative to Sanofi’s Verorab®. The rabies vaccine market is competitive, and this study could potentially shift market dynamics if Sinovac’s vaccine proves effective.
The study is ongoing, with further details available on the ClinicalTrials portal.
