Abstract

BackgroundPublic research organizations and their interactions with industry partners play a crucial role for public health and access to medicines. The development and commercialization of the Human Papillomavirus (HPV) vaccines illustrate how licensing practices of public research organizations can contribute to high prices of the resulting product and affect accessibility to vulnerable populations. Efforts by the international community to improve access to medicines have recognised this issue and promote the public health-sensitive management of research conducted by public research organizations. This paper explores: how medical knowledge is exchanged between public and private actors; what role inventor scientists play in this process; and how they view the implementation of public health-sensitive knowledge exchange strategies.MethodsWe conducted a systematic qualitative literature review on medical knowledge exchange and qualitative interviews with a purposive sample of public sector scientists working on HPV vaccines. We explored the strategies by which knowledge is exchanged across institutional boundaries, how these strategies are negotiated, and the views of scientists regarding public health-sensitive knowledge exchange.ResultsWe included 13 studies in the systematic review and conducted seven semi-structured interviews with high-ranking scientists. The main avenues of public-private medical knowledge exchange were publications, formal transfer of patented knowledge, problem-specific exchanges such as service agreements, informal exchanges and collaborative research. Scientists played a crucial role in these processes but appeared to be sceptical of public health-sensitive knowledge exchange strategies, as these were believed to deter corporate interest in the development of new medicines and thus risk the translation of the scientists’ research.ConclusionMedical scientists at public research institutions play a key role in the exchange of knowledge they generate and are concerned about the accessibility of medicines resulting from their research. Their scepticism towards implementing public health-sensitive knowledge management strategies appears to be based on a biased understanding of the costs and risks involved in drug development and a perceived lack of alternatives to private engagement. Scientists could be encouraged to exchange knowledge in a public health-sensitive manner through not-for-profit drug development mechanisms, education on industry engagement, and stronger institutional and legal backing.

Highlights

  • Public research organizations and their interactions with industry partners play a crucial role for public health and access to medicines

  • Often in contrast to these “academic channels” [66], studies discussed the protection of Intellectual Property (IP) through patents and the subsequent licensing of the protected technologies [65, 67, 74]

  • It was reported that some Public Research Organization (PRO) provide financial incentives to scientists engaging in patenting and commercialization [68]

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Summary

Introduction

Public research organizations and their interactions with industry partners play a crucial role for public health and access to medicines. Public research organizations (PROs) play a crucial role in the advancement of medical science [1]. Almost half of all drug approvals submitted by PROs have received priority review, compared to one in five submissions from the private sector – indicating that research carried out at PROs has a higher public health impact [2]. The contribution of PROs is significant in the field of vaccines – virtually all important and innovative vaccines approved from 1985 to 2010 have been developed by PROs [2] These include the vaccines against Human Papillomavirus (HPV). It is the leading cause of cancer death in women in mainly sub-Saharan Africa and South-Eastern Asia, disproportionately affecting young women in regions where screening and treatment options are limited [4,5,6,7]

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