OR WAIT null SECS
Accurately targeted immunotherapies through reliable neoantigen recognition enable personalized medicine development.
Activation and expansion are essential for success in both autologous and allogeneic therapies.
Continuous manufacturing and a quality-by-design development approach are a natural fit.
November 08, 2024
The companies will work to create climate-friendly pMDIs using Orbia’s low global warming potential propellant.
In the collaboration, the new company, Oblenio Bio, has been granted an exclusive option to license LBL-051, a tri-specific T-cell engager antibody, from Leads Biolabs.
November 07, 2024
A genetic medicines customer has selected the company’s binders for commercial development of the customer’s product.
Automation, miniaturization, and new software algorithms are improving throughput and accuracy.
Synaffix, a Lonza company, has licensed its ADC technology to BigHat Biosciences to be combined with the latter's ML design platform to develop new ADCs
November 01, 2024
CDER Director Patrizia Cavazzoni and CBER Director Peter Marks provided an update on the rare disease innovation hub in a new FDA Voices blog post.
October 31, 2024
The partnership will use ViaNautis’ proprietary polyNaut technology platform to develop genetic medicines that can precisely target tissue types.
October 30, 2024
Webinar Date/Time: Fri, Nov 22, 2024 11:00 AM EST
October 29, 2024
The collaboration aims to advance clinical development of a Phase I drug candidate, MRT-6160, and to explore other therapeutic opportunities across multiple indications.
October 28, 2024
Webinar Date/Time: Tue, Nov 19, 2024 11:00 AM EST