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. 2025 Jan 29;12(Suppl 1):ofae631.1571. doi: 10.1093/ofid/ofae631.1571

P-1395. Safety and Effectiveness of LC16m8 for Pre-Exposure Prophylaxis Against mpox in High-Risk Population: An Open-Label Randomized Trial

Nobumasa Okumura 1, Eriko Morino 2, Hidetoshi Nomoto 3, Mashiho Yanagi 4, Kozue Takahashi 5, Haruka Iwasaki 6, Yukari Uemura 7, Yosuke Shimizu 8, Daisuke Mizushima 9, Kazuaki Fukushima 10, Ei Kinai 11, Daisuke Shiojiri 12, Ichiro Itoda 13, Yasuhiko Onoue 14, Yoshitomo Kobori 15, Fukumi Nakamura 16, Daisuke Tokita 17, Wataru Sugiura 18, Norio Ohmagari 19, Mugen Ujiie 20,1,2,3
PMCID: PMC11779367

Abstract

Background

Since May 2022, the incidence of mpox cases has surged outside endemic regions. Although vaccination remains pivotal in mpox prevention, data on LC16m8, a third-generation smallpox vaccine, are scant. We provided LC16m8 pre-exposure prophylaxis opportunities to high-risk individuals, including those with HIV, and conducted a randomized controlled trial to assess LC16m8’s effectiveness in mpox prevention and safety.

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Methods

Our multicenter randomized open-label trial enrolled men and women aged ≥18 years at high mpox risk who provided written consent. Participants were randomly assigned 1:1 to early or late vaccination groups, receiving vaccinations approximately 70 days apart. Primary endpoint: vaccine effectiveness (VE) against mpox development between early and late vaccinations. VE against severe mpox, symptoms, “take” incidence, and adverse events were secondary endpoints.

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Results

A total of 1,135 participants were recruited; 570 and 565 were assigned to early and late vaccination groups, respectively; 530 and 476 were vaccinated. Median age: 41 years; 99.7% were male; 89.7% Japanese; and 34.4% HIV-infected. No mpox cases occurred during the observation period, precluding VE calculation. “Take” rates: 90.3% (HIV-infected), 94.6% (uninfected). Adverse events related to the study were observed in 96.6% and 98.0% of the HIV-infected and uninfected participants, respectively. No fatal adverse events were observed; serious adverse events (SAE): 0.6% (HIV-infected), 0.5% (uninfected). One HIV-uninfected participant reported pulmonary embolism and deep vein thrombosis as a causally undeniable SAE. Local skin reactions: 96.6% (HIV-infected), 97.9% (uninfected); systemic reactions: 63.6% (HIV-infected), 64.2% (uninfected).

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Conclusion

LC16m8’s effectiveness in mpox prevention remains inconclusive. Yet, its use in well-controlled HIV-infected and -uninfected individuals showed no significant safety concerns, suggesting potential for targeted vaccination strategies in at-risk groups.

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Disclosures

All Authors: No reported disclosures


Articles from Open Forum Infectious Diseases are provided here courtesy of Oxford University Press

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