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.
GSK secures Japan Orphan Drug status for lung cancer ADC
TheraCryf advances lead addiction programme to final preclinical stage
Dizal meets primary endpoint in Phase 3 study of ZEGFROVY (sunvozertinib) monotherapy
Innovent Biologics reports first participant dosed in tigulixostat Phase 3 study
Novartis to acquire PI3K-alpha inhibitor program from Synnovation in deal worth up to USD3bn
Humacyte prices USD20m registered direct offering
Curia expands Glasgow manufacturing capacity and enhances CLD platform
Congruence Therapeutics secures USD39.5m financing
Pfizer reports Phase 3 TALAPRO-3 results showing improved outcomes in metastatic prostate cancer
Mabtech partners with Sai Life Sciences to expand access to EYRA multiplex immunology platform
Mirecule expands collaboration with Sanofi to advance FSHD therapy
Sanofi's venglustat receives FDA Breakthrough Therapy designation for type 3 Gaucher disease
Alebund Pharmaceuticals signs licensing and equity agreements with R1 Therapeutics