Literature DB >> 27484011

Chemistry, manufacturing and control (CMC) and clinical trial technical support for influenza vaccine manufacturers.

Rahnuma Wahid1, Renee Holt1, Richard Hjorth2, Francesco Berlanda Scorza3.   

Abstract

With the support of the Biomedical Advanced Research and Development Authority (BARDA) of the US Department of Health and Human Services, PATH has contributed to the World Health Organization's (WHO's) Global Action Plan for Influenza Vaccines (GAP) by providing technical and clinical assistance to several developing country vaccine manufacturers (DCVMs). GAP builds regionally based independent and sustainable influenza vaccine production capacity to mitigate the overall global shortage of influenza vaccines. The program also ensures adequate influenza vaccine manufacturing capacity in the event of an influenza pandemic. Since 2009, PATH has worked closely with two DCVMs in Vietnam: the Institute of Vaccines and Medical Biologicals (IVAC) and VABIOTECH. Beginning in 2013, PATH also began working with Torlak Institute in Serbia; Instituto Butantan in Brazil; Serum Institute of India Private Ltd. in India; and Changchun BCHT Biotechnology Co. (BCHT) in China. The DCVMs supported under the GAP program all had existing influenza vaccine manufacturing capability and required technical support from PATH to improve vaccine yield, process efficiency, and product formulation. PATH has provided customized technical support for the manufacturing process to each DCVM based on their respective requirements. Additionally, PATH, working with BARDA and WHO, supported several DCVMs in the clinical development of influenza vaccine candidates progressing toward national licensure or WHO prequalification. As a result of the activities outlined in this review, several companies were able to make excellent progress in developing state-of-the-art manufacturing processes and completing early phase clinical trials. Licensure trials are currently ongoing or planned for several DCVMs.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Clinical trial implementation; Influenza vaccine manufacturing; Quality management systems

Mesh:

Substances:

Year:  2016        PMID: 27484011     DOI: 10.1016/j.vaccine.2016.07.046

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  2 in total

1.  Safety and immunogenicity of a seasonal trivalent inactivated split influenza vaccine: a phase I randomized clinical trial in healthy Serbian adults.

Authors:  Goran Stevanovic; Lidija Lavadinovic; Svetlana Filipovic Vignjevic; Renée Holt; Katarina Ilic; Francesco Berlanda Scorza; Erin Sparrow; Vera Stoiljkovic; Guido Torelli; Tamra Madenwald; Muriel Socquet; Aleksandra Barac; Yordanka Ilieva-Borisova; Mijomir Pelemis; Jorge Flores
Journal:  Hum Vaccin Immunother       Date:  2018-02-23       Impact factor: 3.452

2.  Technology transfer programme for influenza vaccines - Lessons from the past to inform the future.

Authors:  Christopher Chadwick; Martin Friede; Ann Moen; Claudia Nannei; Erin Sparrow
Journal:  Vaccine       Date:  2022-07-07       Impact factor: 4.169

  2 in total

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