Human Dosing of Self-Replicating mRNA-Based COVID-19 Vaccine Candidate to Begin Soon

By HospiMedica International staff writers
Posted on 24 Jul 2020
Human dosing of a self-replicating mRNA-based-COVID-19 vaccine candidate is all set to begin soon after new preclinical data demonstrated that neutralizing antibody titres continued to increase for 50 days after a single administration.

Arcturus Therapeutics Holdings Inc. (San Diego, CA, USA) and Duke-NUS Medical School (Singapore) have received approval from the Singapore Health Sciences Authority of their clinical trial application for their COVID-19 vaccine candidate, LUNAR-COV19. Arcturus and Duke-NUS are jointly developing the coronavirus vaccine using Arcturus’ STARR technology and a unique platform developed at Duke-NUS allowing rapid screening of vaccines for potential effectiveness and safety.

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The STARR Technology platform employed in LUNAR-COV19 combines self-replicating mRNA with LUNAR, a proprietary nanoparticle delivery system optimized for mRNA molecules. The efficiency and self-replicating nature of the approach were designed to enable very low doses, and a potential single vaccine administration. Prior animal data has demonstrated robust humoral and cellular immunity elicited at doses as low as 0.2 µg of LUNAR-COV19. Additionally, Arcturus demonstrated 100% seroconversion for anti-SARS-CoV-2 neutralizing antibodies with a very low single dose (2.0 µg). New preclinical data demonstrate that neutralizing antibody levels in response to a single administration of LUNAR-COV19 (0.2, 2.0, 10.0 µg) continue to increase over 50 days. The increasing antibody levels are attributed to the self-replicating mRNA of LUNAR-COV19. These results were obtained using a Luminex bead assay. A 1/2000 serum dilution was assayed for neutralizing IgG antibodies in the mouse serum every 10 days for 60 days post vaccination.

Arcturus and Duke-NUS will now initiate human dosing of LUNAR-COV19 as soon as possible. The healthy volunteer study will evaluate several dose levels of LUNAR-COV19 in up to 108 adults, including older adults. Follow-up will be conducted to evaluate safety, tolerability and the extent and duration of the humoral and cellular immune response.

“The approval of the Clinical Trial Application for LUNAR-COV19 is a critical milestone for Arcturus. We are excited to advance this promising vaccine candidate into clinical trials. Based on our preclinical data, we believe that our self-replicating mRNA-based approach may produce high rates of seroconversion and robust T-cell induction with a potential single administration, at very low doses. The LUNAR-COV19 profile is meaningfully differentiated and may facilitate the mass vaccine campaigns necessary to target hundreds of millions of individuals globally,” said Joseph Payne, President and CEO of Arcturus.

“Preclinical studies on LUNAR-COV19 have shown very promising findings, including the possibility that a single dose of this vaccine may be sufficient to trigger robust and durable immune responses against SARS-CoV-2. We are very eager to start the first-in-human clinical trial here in Singapore and advance LUNAR-COV19 on its journey to becoming a potential commercial vaccine,” said Professor Ooi Eng Eong, Deputy Director of the Emerging Infectious Diseases Program at Duke-NUS.

Related Links:
Arcturus Therapeutics Holdings Inc.
Duke-NUS Medical School



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