Close
Smartlab Europe
Inizio Ignite

Wheeler Bio $31M in Financing to Support Clinical Drug Substance Mfg. Facility

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Related stories

Injectable Drug Formulation Trends in Biopharma

Analysis of the evolving landscape of parenteral delivery, focusing on the stability of high-concentration biologics and the integration of patient-centric delivery devices.

ACG Packaging Materials Joins WEF Global Lighthouse Network

ACG Packaging Materials has announced that its Shirwal manufacturing...

Future Trends in Pharmaceutical Drug Delivery Platforms

Forward-looking perspective on the convergence of digital technology, bioengineering, and material science in creating the next generation of therapeutic delivery systems.
- Advertisement -

Wheeler Bio, Inc., a CDMO specializing in process development and small batch cGMP production of therapeutic antibodies, announced the closing of their Series A financing round. The company will use the funding to complete its state-of-the-art cGMP cell banking and drug substance manufacturing facility (500 L scale) in The Ziggurat, an Oklahoma City office tower. The first cGMP production batches in the new facility will begin in 3Q23.

The round was co-led by Charles River Laboratories and Echo, with participation from ATUM, Floating Point Advisors, Pine Ridge Ventures, Plains Venture Partners, Seagull Capital, and Alloy Therapeutics.

According to the company, it’s building a disruptive CDMO model that is changing the paradigm for the gene-to-IND supply chain. Their primary service offering, Portable CMC, is an open source “CMC middleware” designed to deliver speed, efficiency, predictability, and freedom to operate by integrating discovery CROs and CDMOs and bridging the translational gap.

Portable CMC includes integrated development services, including manufacturability assessments, stable pool and clone development, process and analytical method development, process demonstration, and technology transfer into cGMP production.

The platform aims to enhance key business integrations that speed up the translational steps for clients while lowering technical, regulatory, and business risks.

“Wheeler is at the forefront of phase-appropriate CMC drug development programming. We serve clients and partners with cutting-edge development services, including Portable CMC,” said Jesse McCool, Co-Founder and CEO at Wheeler Bio. “The Series A validates our thesis that developers of next-gen therapeutic proteins want access to more focused development and manufacturing resources with high agility and small batch sizes to be successful. We are intentionally staying inside of the box.”

Brian Berquist, chief development officer at Wheeler Bio said, “Wheeler is laser-focused on translational CMC while solving for clients’ timelines and budgets along the way to first-in-human studies. Our platform reduces risk by enhancing product and process knowledge gained using well-integrated tools, technologies, and digital solutions like Leap-In Transposase, Solentim, Ambr Microbioreactors, DynaDrive Single-Use Bioreactors, the Synthace Experiment Platform, and DataHowLab.”

“Wheeler Bio’s advancements and continued growth embody Echo’s aim to reestablish American manufacturing jobs, reinforce critical industries, and solve problems for coastal companies by connecting overlooked domestic resources,” said Christian Kanady, co-Founder at Wheeler Bio and Founding Partner at Echo. “Alongside respected partners, Wheeler Bio is connecting Oklahoma City with the global industry, accelerating drug development, and unlocking our region’s comparative advantages.”

Latest stories

Related stories

Injectable Drug Formulation Trends in Biopharma

Analysis of the evolving landscape of parenteral delivery, focusing on the stability of high-concentration biologics and the integration of patient-centric delivery devices.

ACG Packaging Materials Joins WEF Global Lighthouse Network

ACG Packaging Materials has announced that its Shirwal manufacturing...

Future Trends in Pharmaceutical Drug Delivery Platforms

Forward-looking perspective on the convergence of digital technology, bioengineering, and material science in creating the next generation of therapeutic delivery systems.

Advancing Drug Formulation Stability in Modern Pharma

Exploration of the chemical, physical, and environmental factors that compromise the integrity of modern therapeutics, and the advanced testing protocols used to ensure safety.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Translate »