Register Now: From Clinical to Commercial: Accelerating ADC Late-Stage Development with Technology Innovation and Integrated Platform
|Articles|July 19, 2022

TFF Pharmaceuticals Expands R&D Operations with New Facility

TFF Pharmaceuticals is expanding its R&D operations with a new facility in Austin, Texas.

TFF Pharmaceuticals announced on July 14, 2022 that it is significantly expanding its R&D operations through the lease of a new research and development facility located in Austin, Texas.

The 3,500-ft2 facility will increase TFF’s total lab space, adding a dedicated lab for downstream processing of products created via its Thin Film Freezing technology. The facility will also allow for more space to accommodate larger equipment to facilitate scale-up and manufacturing as well as product supplies for preclinical studies.

The company also plans to expand the product development team in Austin, which will be based at the new facility to support the company’s growing number of partnered projects. The facility will be supervised by Donald Owens, PhD, director of product development at TFF and supported by John Koleng, PhD, vice-president of product development and manufacturing.

“The opening of our new Austin R&D facility represents an important evolution of TFF’s operations, reflecting growing demand for our Thin Film Freezing technology and product development services,” Koleng said in a company press release. “The Austin facility will enable us to increase testing capacity so that we can run a larger number of feasibility studies, including a focus on biologics where demand has continued to grow. Additionally, as many of our partnered programs move to clinical evaluation, the ability to scale-up manufacturing in parallel becomes mission critical. We expect the new Austin facility will allow us to meet the current growing demand for Thin Film Freezing-based products.”

Source: TFF Pharmaceuticals


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.