Novel Influenza Vaccines: From Research and Development (R&D) Challenges to Regulatory Responses

Author:

He Xiangchuan123,Zhang Tianxiang12,Huan Shitong4,Yang Yue12

Affiliation:

1. School of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China

2. Key Laboratory of Innovative Drug Research and Evaluation, National Medical Products Administration, Beijing 100084, China

3. Tsinghua-Peking Center for Life Sciences, Beijing 100084, China

4. China Office, The Bill & Melinda Gates Foundation, Beijing 100084, China

Abstract

Influenza vaccines faced significant challenges in achieving sufficient protective efficacy and production efficiency in the past. In recent decades, novel influenza vaccines, characterized by efficient and scalable production, advanced platforms, and new adjuvant technologies, have overcome some of these weaknesses and have been widely licensed. Furthermore, researchers are actively pursuing the development of next-generation and universal influenza vaccines to provide comprehensive protection against potential pandemic subtypes or strains. However, new challenges have emerged as these novel vaccines undergo evaluation and authorization. In this review, we primarily outline the critical challenges and advancements in research and development (R&D) and highlight the improvements in regulatory responses for influenza vaccines.

Funder

Bill and Melinda Gates Foundation

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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