Register Now: From Clinical to Commercial: Accelerating ADC Late-Stage Development with Technology Innovation and Integrated Platform
|Articles|November 1, 2019

Evonetix Relocates to New Facility in Cambridge, UK

The new facility is 15,000 ft2, which includes 8000 ft2 of lab space and 7000 ft2 of office space.

Evonetix, a synthetic biology company previously located in Chesterford Research Park, United Kingdom, announced it relocated to a new facility in Coldham’s Business Park, Cambridge, UK on Oct. 30, 2019.

The new facility is 15,000 ft2, which includes 8000 ft2 of lab space and 7000 ft2 of office space, the company said in a press release. The company currently houses 40 employees and will look to recruit further staff to join its teams of physicists, electronics and software engineers, chemists, biologists, and molecular biologists at its new location.

“Synthetic biology has the potential to solve some of the world’s most intractable problems, but we require innovation in gene synthesis to accelerate progress,” said Dr. Tim Brears, Evonetix CEO, in the press release. “Our new office and lab space will enable integration of our teams of specialists to support the development and delivery of our highly parallel desktop platform, which will be available to every researcher to accelerate their ability to use biology on a scale not currently possible.”

Source: Evonetix

 

 

 


Related to this article

The BioPharm Brief: An AI-Designed Multibody ADC Enters the Clinic, Blackstone Backs Pfizer’s Monthly GLP-1, and enGene Readies a Bladder Cancer BLA
FDA clears the IND for Biolojic Design’s BD200, an AI-designed Trop2/Nectin-4 multibody ADC; Blackstone Life Sciences agrees to provide Pfizer up to $1.5 billion to develop its monthly GLP-1 receptor agonist berobenatide; and enGene Therapeutics plans a year-end BLA for detalimogene voraplasmid in BCG-unresponsive non-muscle invasive bladder cancer.
The BioPharm Brief: FDA Designations for a Bispecific CAR-T, a BLA for Friedreich’s Ataxia, and Phase 2b MASH Data for Efinopegdutide
FDA grants RMAT and Fast Track designations to AbelZeta’s CD20/CD19 bispecific CAR-T prizlon-cel in relapsed or refractory large B-cell lymphoma, Larimar Therapeutics completes a BLA seeking accelerated approval of nomlabofusp for Friedreich’s ataxia, and Merck’s GLP-1/glucagon receptor agonist efinopegdutide meets its primary endpoint in a phase 2b MASH trial.