Source: Pharmaceutical Technology
Source: Pharmaceutical Technology
The collaboration is aimed at discovering and developing new advanced treatments for genitourinary (GU) tumours as well as other related serious diseases using ReviR’s RNA-targeted technologies. Under the agreement, Asieris will use the advanced RNA modulation technologies, Binder and SpliceR, of ReviR for identifying and developing new therapies that target RNA for cancer treatment. ReviR combines computational and high throughput drug discovery technologies to deliver advanced medicines to patients.
The company’s VoyageR AI platform integrates computational methods to drug traditionally undruggable RNA targets.
Its initial focus is to develop therapeutics in oncology, CNS, and genetically defined disease indications.
ReviR Therapeutics chief scientific officer Paul August said: “Asieris is a global biopharma company specialised in the development of GU oncology therapies, and we are excited to be working with them to discover new treatments for indications of interests. “Our BindeR and SpliceR platform technologies have the potential to advance therapeutics for undruggable cancer targets, and we believe this collaboration will accelerate the discovery of new treatments for patients.”
The company is focused on developing RNA-targeting small molecule therapies to treat cancer and other serious genetically defined diseases.
It uses technologies to develop therapeutics that modulate the target RNA, to develop disease-modifying treatments.
“We believe that our in-house R&D expertise on small molecule oncology drug discovery, combined with ReviR’s proprietary RNA-targeted technologies, will speed the benefit to patients.
“We will continue to adhere to our differentiated R&D strategy, focus on genitourinary tumours and related diseases, and expand the global reach of our innovation to deliver novel drug products for patients in China and globally.” Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva.
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Optimise your cell therapy process: a guide to cell thawing
Typically carried out at the point of care, errors in cell therapy thawing could compromise treatment efficacy, leading to significant patient impact as well as high costs and a compromised reputation for the product’s developer.
This guide addresses how cell thawing has historically developed into the new techniques used today, along with the physical and biological implications of key metrics and components such as warming rate and ice structure. Also included are reviews of key studies from scientific literature and a consideration of the interactions between cooling and warming rates, as applicable to cell and gene therapies.
Source: Pharmaceutical Technology
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