News

Curate Biosciences launches its first product to transform cell therapy manufacturing costs and performance

Curate Biosciences  announced the commercial launch of its Curate® Cell Processing System. The first-of-its-kind Curate System produces better starting materials for CAR-T cancer therapies and other cell therapies. Its exceptionally gentle microfluidic process recovers about 90% of white blood cells with elimination of more than 90% of red cells and 99% of platelets from patient-sourced leukapheresis blood product, delivering cells that support increased transduction efficiency for therapy manufacturing. Over the past year, in advance of the launch, the company has provided the Curate System for external testing at more than ten leading cell therapy sites across industry, academia, and government. These third-party evaluations have confirmed the superiority of the system’s performance, its ease of use, and its value to cell therapy manufacturing.

The Curate Cell Processing System uses the company’s proprietary Deterministic Cell Separation™ microfluidic technology, which is gentle to the cells while delivering unparalleled recovery and purity of target white blood cells. The Curate System has been designed to minimize labor skill requirements and hands-on time, processing a Leukopak of blood cells in ~45 minutes in a single pass. Cell therapy manufacturers will be able to incorporate the advanced Curate System in their workflow to improve end-to-end processing, reducing overall cost, time-to-dose, and potential for production failures. The product launch today is an enabling step, as the Curate System is a keystone to providing more affordable and accessible next-generation therapies to treat and even cure intractable diseases.

Current cell isolation methods used in cell therapy production require high physical forces and chemical reagents that lose 30-40% of patient-donated white blood cells, on average, before gene transfer takes place. That upfront cell loss adds days and substantial cost as drugmakers must then increase the cell population to reach a required dose level of genetically modified cells, which impacts therapeutic efficacy. For late-stage cancer patients who have not had success with other treatments, shortening the time to produce these therapies is critical, and each additional production day dramatically increases costs. The Curate System alleviates these core industry concerns.

“The Curate System’s entry into the market promises to transform approaches to making a cell therapy, by delivering near-complete recovery of white blood cells with second-to-none purity and increased patient sample-to-sample consistency,” said David Backer, Curate Biosciences’ new CEO. “New customers will discover what our early-access biopharma and academic partners have already seen: our microfluidic approach outperforms today’s standard methods.”

“We’re excited to see years of investment, support from NIH, and the hard work of our fantastic team leading to this moment,” said Founder & Chairman Mike Grisham. “The company has gained feedback from users, finalized the product and is growing our commercial team, so our Curate® Cell Processing System can help accelerate broad deployment of emerging cell therapies.”

Read more here.

Recent News

06/11/2026

Adial Pharmaceuticals Announces Acquisition of Azora Therapeutics and up to $64 Million Financing

Adial Pharmaceuticals, Inc. (Nasdaq: ADIL) (“Adial” or the “Company”) today announced that it has acquired Azora Therapeutics, Inc. (“Azora”), a biopharmaceutical company developing treatments for serious inflammatory diseases. The acquisition brings Azora’s lead asset AT177, a proprietary colon‑targeted aryl hydrocarbon receptor (AhR) agonist designed to enable localized activation with limited systemic exposure, into Adial’s pipeline.

06/11/2026

Luna Labs Launches 3 Waves Venture Spinout to Commercialize Advanced Vestibular Stimulation Technology

Luna Labs today announced the launch of 3 Waves, Inc. (“3Waves”), a dual-use spinout company that was established to commercialize advanced virtual and mixed reality technologies for defense, commercial simulation, and medical applications. As part of the spinout, 3Waves and Mayo Clinic executed an exclusive license to support the development of next-generation vestibular stimulation systems

06/02/2026

TearSolutions Receives FDA Orphan Drug and Fast Track Designations for Lacripep® in Neurotrophic Keratitis and Initiates Phase 2 Clinical Trial with First Patients Dosed

TearSolutions, Inc. (“TearSolutions”), a clinical-stage biotechnology company developing novel ophthalmic therapeutics, today announced receiving Food and Drug Administration (FDA) Orphan Drug (ODD) and Fast Track Designations for Lacripep in Neurotrophic Keratitis (NK) and initiating a Phase 2 clinical trial with first patients dosed. The FDA’s ODD provides incentives, including tax credits for clinical testing and