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Implications of the Licensure of a Partially Efficacious Malaria Vaccine on Evaluating Second-generation Vaccines

Overview
Journal BMC Med
Publisher Biomed Central
Specialty General Medicine
Date 2013 Nov 16
PMID 24228861
Citations 8
Authors
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Abstract

Background: Malaria is a leading cause of morbidity and mortality, with approximately 225 million clinical episodes and >1.2 million deaths annually attributed to malaria. Development of a highly efficacious malaria vaccine will offer unparalleled possibilities for disease prevention and remains a key priority for long-term malaria control and elimination.

Discussion: The Malaria Vaccine Technology Roadmap's goal is to 'develop and license a first-generation malaria vaccine that has protective efficacy of more than 50%'. To date, malaria vaccine candidates have only been shown to be partially efficacious (approximately 30% to 60%). However, licensure of a partially effective vaccine will create a number of challenges for the development and progression of new, potentially more efficacious, malaria vaccines in the future. In this opinion piece we discuss the methodological, logistical and ethical issues that may impact on the feasibility and implementation of superiority, non-inferiority and equivalence trials to assess second generation malaria vaccines in the advent of the licensure of a partially efficacious malaria vaccine.

Conclusions: Selecting which new malaria vaccines go forward, and defining appropriate methodology for assessment in logistically challenging clinical trials, is crucial. It is imperative that the scientific community considers all the issues and starts planning how second-generation malaria vaccines will advance in the advent of licensure of a partially effective vaccine.

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References
1.
OMeara W, Mwangi T, Williams T, McKenzie F, Snow R, Marsh K . Relationship between exposure, clinical malaria, and age in an area of changing transmission intensity. Am J Trop Med Hyg. 2008; 79(2):185-91. PMC: 2547116. View

2.
Duncan C, Hill A . What is the efficacy of the RTS,S malaria vaccine?. BMJ. 2011; 343:d7728. PMC: 3287289. DOI: 10.1136/bmj.d7728. View

3.
Postema A, Myers M, Breiman R . Challenges in the development, licensure, and use of combination vaccines. Clin Infect Dis. 2001; 33 Suppl 4:S261-6. DOI: 10.1086/322560. View

4.
Kester K, Cummings J, Ofori-Anyinam O, Ockenhouse C, Krzych U, Moris P . Randomized, double-blind, phase 2a trial of falciparum malaria vaccines RTS,S/AS01B and RTS,S/AS02A in malaria-naive adults: safety, efficacy, and immunologic associates of protection. J Infect Dis. 2009; 200(3):337-46. DOI: 10.1086/600120. View

5.
Agnandji S, Lell B, Soulanoudjingar S, Fernandes J, Abossolo B, Conzelmann C . First results of phase 3 trial of RTS,S/AS01 malaria vaccine in African children. N Engl J Med. 2011; 365(20):1863-75. DOI: 10.1056/NEJMoa1102287. View