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Review
. 2024 Oct 19;31(7):taae123.
doi: 10.1093/jtm/taae123.

From bench to clinic: the development of VLA1553/IXCHIQ, a live-attenuated chikungunya vaccine

Affiliations
Review

From bench to clinic: the development of VLA1553/IXCHIQ, a live-attenuated chikungunya vaccine

Lin H Chen et al. J Travel Med. .

Abstract

Background: Over the past 20 years, over 5 million cases of chikungunya, a mosquito-transmitted viral disease, have been reported in over 110 countries. Until recently, preventative strategies for chikungunya were largely ineffective, relying on vector control and individual avoidance of mosquito bites.

Methods: This review outlines the preclinical and clinical efficacy and safety data that led to the approval of VLA1553 (IXCHIQ®), a live-attenuated vaccine against chikungunya disease. It also describes the innovative development pathway of VLA1553, based on an immunological surrogate of protection, and discusses ongoing and future post-licensure studies.

Results: In mice and non-human primate models, VLA1553 elicited high titres of neutralizing antibodies, conferred protection against wild-type chikungunya virus challenge and raised no safety concerns. A Phase 1 clinical trial of VLA1553 demonstrated 100% seroconversion among 120 healthy participants, with sustained neutralizing antibody titres after 12 months. These results and determination of a surrogate marker of protection led to advancement of VLA1553 directly into Phase 3 clinical development, as agreed with the US Food and Drug Administration (FDA) and the European Medicines Agency. The pivotal Phase 3 trial met its primary immunogenicity endpoint, achieving seroprotective levels based on immuno-bridging in baseline seronegative participants 28 days post-vaccination. These findings enabled submission of a Biologics Licence Application to the FDA for accelerated approval of VLA1553 in the US for adults aged ≥18 years. Ongoing and planned studies will confirm the clinical efficacy/effectiveness and safety of VLA1553 in adults and younger individuals, and will generate data in chikungunya endemic countries that have the highest unmet need.

Conclusion: VLA1553 is the first vaccine approved for the prevention of chikungunya disease in adults, following accelerated development based on a serological surrogate marker of protection. VLA1553 adds to strategies to reduce the spread and burden of chikungunya in endemic populations and travellers.

Keywords: VLA1553; arbovirus; chikungunya; immunogenicity; safety; surrogate of protection; vaccine.

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Conflict of interest statement

L.C. has received honoraria or advisor fees from Shoreland Inc, Valneva (not for this work), Takeda, Bavarian Nordic and MSD.

K.D. was a Valneva employee and owns stock options in Valneva.

A.F., R.H. and S.M. are Valneva employees and own stock and share options in Valneva.

Figures

Figure 1
Figure 1
Surrogate of protection determination by analysing samples from NHP passive transfer study (A) and confirmation of surrogate of protection by analysing samples from Yoon et al. (B). A. Peak viraemia titres plotted against μPRNT50 titres from the NHP passive transfer study. Horizontal dotted lines show LLOQ (500 copies/mL) and LLOD (60 copies/mL) of the qPCR. Vertical dotted lines show μPRNT50 titres of 50 and 100, while the vertical solid line μPRNT50 titre of 150. B. Comparison of neutralization antibody titre results measured by μPRNT50 assay or reported by PRNT80 assay (Yoon et al.49). CI, confidence interval; LLOD, lower limit of detection; LLOQ, lower limit of quantification; NHP, non-human primate; PRNT, plaque reduction neutralization test; PRNT80, neutralization titre using an 80% plaque reduction; qPCR, quantitative polymerase chain reaction; μPRNT50, neutralization titre determined in a micro-neutralization assay (96 well format) using a 50% plaque reduction. Figure 1A is adapted from under the terms of the Creative Commons Attribution 4.0 International Licence (https://creativecommons.org/licenses/by/4.0/deed.en).
Figure 2
Figure 2
Assessment of CHIKV-specific neutralizing antibodies GMTs after vaccination, stratified by study day and age from the pivotal Phase 3 trial (per protocol population). Days shown in the figure refer to study days; Day 1 = day of vaccination. Error bars indicate 95% CIs. Neutralizing antibodies to the vaccine were evaluated from clinical specimen (human serum) using μPRNT50. CI, confidence interval; GMT, geometric mean titre; μPRNT50; neutralization titre determined in a micro-neutralization assay (96 well format) using a 50% plaque reduction.
Figure 3
Figure 3
VLA1553 development pathway. ACIP, Advisory committee on immunization practices; BLA, Biologics Licence Application; CEPI, Coalition for Epidemic Preparedness Innovations; EMA, European Medicines Agency; FDA, US Food and Drug Administration; NHP, non-human primate; PRIME, PRIority Medicines; R&D, research and development.

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