An interim analysis of the data found that 93% of subjects previously vaccinated with Pfizer (NYSE: PFE), Moderna, Johnson and Johnson (Janssen) (NYSE: JNJ), and AstraZeneca vaccines showed an increase in neutralizing antibody titers after receiving a single dose of AKS-452.
The average neutralization titers across all subjects increased 4-fold against the Wuhan strain and 5-fold against the Omicron variants at Day 28.
There were no safety issues reported.
The non-randomized, open-label, safety, and efficacy study was conducted and managed by TRACER Europe B.V., a CRO specializing in fast-track clinical trials that previously conducted Phase I and II trials for AKS-452 in the Netherlands.
Seventy healthy participants between the ages of 18 and 85 received one 90 µg dose of the AKS-452 antigen.
The vaccine was well tolerated with data indicating a favorable safety profile, similar to that of the registered vaccines.
Antibody levels, virus neutralization activity, and T cell response will be measured at intervals over the next nine months.
A 1,600 subject Phase II/III clinical trial of AKS-452 as a two-dose primary vaccine was completed earlier this year in India.
The positive results from that study have been submitted as part of an Emergency Use Application in India.
AKS-452 is a second-generation vaccine based on Akston's novel Fc-fusion platform. Its composition provides direct presentation to the immune system and robust protection against virus variants.
Using proven antibody technologies, it inherently supports high production yields and stability at high temperatures.
Tracer Europe B.V. is a Clinical Research Organization specializing in fast-track solutions for testing innovative biologic medicines and is a founding member of the COVID-19 Rapid Cure Task Force.
Tracer and its partners provide its clients with the expertise, infrastructure, and capacity to rapidly generate accurate first-in-human clinical data.
Akston Biosciences Corp. leverages its novel Fc-fusion protein platform to develop and manufacture new classes of biologics, including vaccines, ultra-long-acting insulins, and autoimmune disease therapies.
Founded by the team that developed the world's first clinical glucose-responsive insulin at SmartCells, Inc. (sold to Merck and Co.), Akston owns and operates a GMP biologics cleanroom facility that manufactures kilogram-scale batches of drug substance.
This, along with its research and process development laboratories, are located at its Beverly, Mass. location.
UCB reports positive Phase 3 results for fenfluramine in CDKL5 deficiency disorder
WuXi AppTec's Nantong site receives 2025 Architizer A+Award
MGI partners with Negedia to enhance genomic sequencing in Italy
Speranza Therapeutics partners with Sunshine Labs for harm reduction solutions
CARsgen Therapeutics' satri-cel NDA accepted by Chinese regulator
Sanofi receives FDA orphan drug designation for riliprubart in transplant rejection
Aptamer Group signs development and licensing deal with global life sciences partner
Scancell expands Phase 2 SCOPE trial with new intradermal dosing arm for iSCIB1+
Telix Pharmaceuticals delivers first commercial doses from Belgian manufacturing hub
CivicaScript introduces low-cost multiple sclerosis treatment
Innovent presents mazdutide Phase 3 clinical study results at ADA 85th Scientific Sessions
Hoth Therapeutics reports positive interim results for HT-001 topical therapy
Hemab Therapeutics presents bleeding disorder clinical and preclinical data at ISTH 2025 Congress