Global inequities in representation of low-income and middle-income countries in vaccine clinical trials: protocol for a systematic review and meta-epidemiological analysis.

内容摘要

Vaccines are among the most cost-effective public health interventions and remain central to global strategies for preventing and controlling infectious diseases. Evidence generated from clinical trials informs policy decisions regarding vaccine development, regulatory approval and large-scale implementation. The low-income and middle-income countries (LMICs) bear a disproportionately higher burden of vaccine-preventable diseases and are frequently the primary targets of global immunisation programmes. In spite of this, there have been long-standing concerns regarding inequities in the geographical distribution of vaccine clinical trials. Such inequities may limit the external validity and generalisability of trial findings for LMIC settings.This systematic review and meta-epidemiological analysis aims to assess the representation of LMICs in global vaccine clinical trials and to examine patterns associated with trial characteristics, sponsorship, funding source and time. This systematic review protocol was developed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P) 2015 statement. Eligible studies will be identified through comprehensive searches of bibliographic databases, including MEDLINE (via PubMed), Embase, Web of Science Core Collection, Scopus and the Cochrane Central Register of Controlled Trials, as well as clinical trial registries, including the WHO International Clinical Trials Registry Platform, ClinicalTrials.gov, the EU Clinical Trials Register, the Pan African Clinical Trials Registry and ISRCTN. Published and unpublished phase I-IV interventional vaccine clinical trials conducted on human participants will be eligible without restrictions on disease area, vaccine platform, language or publication status.Title, abstract and full-text screening will be conducted independently by two reviewers. Trial-level data on geographical location, trial phase, vaccine type, study design, sponsor type, funding source, participant distribution and publication status will be extracted using a standardised form. The primary unit of analysis will be the individual clinical trial. Descriptive and meta-epidemiological analyses will be undertaken to assess patterns of LMIC representation. Multivariable logistic regression analyses will be conducted, where appropriate, to identify trial-level factors associated with LMIC participation.The primary outcome will be the proportion of vaccine clinical trials including at least one LMIC study site. Secondary outcomes will include geographical distribution by income group and region, representation by trial phase, vaccine category and platform, sponsor and funding source, temporal trends in LMIC participation, and reporting transparency assessed through concordance between trial registry records and published reports. Ethical approval is not required because this review will use publicly available data and will not involve human participants. Findings will be disseminated through peer-reviewed publications and presentations at scientific and policy forums. CRD420261295568.