Why is Hong Kong exempting Sinovac from publishing clinical trial results?

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Hong Kong Exempts Sinovac from Clinical Trial Publication Due to Urgency

Hong Kong's government has exempted Sinovac from the requirement to publish its third-phase clinical trial results in medical journals. This decision was made in light of the pressing need for vaccination. In contrast, the Pfizer/BioNTech vaccine underwent a different review process, necessitating prior publication of its trial results in a medical journal before examination by the advisory panel.
Urgency as Justification for Exemption

The exemption for Sinovac was explicitly attributed to the "urgency" for vaccination. This implies that the regulatory body prioritized the swift deployment of the vaccine to address immediate public health needs. The urgency factor allowed for a departure from the standard protocol that typically requires peer-reviewed data for such assessments.
Standard Procedure for Pfizer/BioNTech

The process for the Pfizer/BioNTech vaccine, which was the first to be approved by Hong Kong's Health department, involved a more conventional scientific review. This vaccine was mandated to have its third-phase clinical trial results published in a medical journal. This publication requirement serves as a critical step in the validation and examination process by advisory panels.
Advisory Panel Recommendation

The advisory panel on Covid-19 vaccines in Hong Kong has indicated it will recommend the Sinovac vaccine for emergency use. This recommendation moves the Sinovac vaccine closer to formal approval within the territory. The final decision on whether to officially approve the vaccine rests with the city's Health Secretary, Sophia Chan.

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Why is Hong Kong exempting Sinovac from publishing clinical trial results?

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