Under the terms of this agreement, Airway receives worldwide commercial rights to use Glycotope's proprietary cell line technology, GlycoExpress [GEX], to produce AT-100 (rhSP-D), one of Airway's development programmes.
The GlycoExpress technology has been shown to be well suited to the development and large-scale manufacturing of a range of biologics, including antibodies as well as complex and difficult to express proteins.
The Glycotope cell line is designed to optimize the manufacturing of AT-100. Advantages include high-yield production of AT-100, fast production cycles and the provision of human glycosylation patterns on the final protein product. The extraordinarily efficient cell line has produced high-quality protein and will serve as the basis for the production of Airway's protein for use in humans.
Founded in 2011 as a spin-out of Cincinnati Children's Hospital Medical Center, Airway Therapeutics has expertise in protein development for applications in the lungs and pediatrics.
The company is currently developing an investigational product, AT-100, a recombinant form of human surfactant protein-D (rhSP-D), for the prevention of a serious lung condition called bronchopulmonary dysplasia in preterm neonates.
Glycotope focuses on the development of innovative immune-oncological products for the treatment of various cancer types using their GlycoBody and GlycoExpress technologies. Glycotope has currently two products in advanced clinical development.
The company's additional pipeline includes preclinical non-antibody and antibody biopharmaceuticals for various indications.
Glycotope's GlycoExpress platform allows glyco-optimization and high yield production of a variety of fully human glycosylated biopharmaceuticals such as coagulation factors, cytokines, glycoprotein hormones and antibodies by using a toolbox of glyco-engineered proprietary human cell lines that allow for optimisation of a whole series of different determining sugars. In addition, the GEX platform can be used for in process glycosylation control.
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Frontage expands early phase clinical research capabilities across US and China
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
InSysBio agrees new collaborative project with BeOne Medicines
Physiomics secures new modelling contract with Numab Therapeutics
Mabwell reports first patient dosed with 7MW4911 in US trial
Atossa Therapeutics' founder and CEO named one of The Top 50 Healthcare Technology CEOs of 2025
Avacta secures FDA clearance for second pre|CISION oncology programme
Guardant Health and Merck enter multi-year oncology diagnostics collaboration
Akeso secures NMPA review acceptance for gumokimab in ankylosing spondylitis