No Carolina / NY / Florida
Ph: 561.316.3330

No Carolina | NY | Florida

XT-Thrive® Drug Master File (DMF) Accepted by the FDA | Reports X-Therma

Summation

  • X-Therma clients who use the product to preserve therapeutic cells will be able to reference the DMF in their Investigational New Drug (IND) and Biologics License Application (BLA) submissions to the FDA for products in the Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER).
  • , a biotechnology company developing a breakthrough platform for regenerative medicine and organ preservation, announces that the Food and Drug Administration (FDA) accepted a Drug Master File (DMF) covering its product, XT-Thrive®.
  • XT-Thrive® is a DMSO-free, serum-free, protein-free, and chemically defined cryopreservation media enabling the preservation of mammalian cells at ultra-low temperatures (-70° C to -196° C).

X-Therma Inc

X-Therma Inc., a biotechnology company developing a breakthrough platform for regenerative medicine and organ preservation, announces that the Food and Drug Administration (FDA) accepted a Drug Master File (DMF) covering its product, XT-Thrive®. This DMF covers the Chemistry, Manufacturing and Controls (CMC) for this key chemistry innovation, which enables non-toxic cryopreservation for life-saving regenerative medicines.

Xiaoxi Wei, Ph.D., co-founder and Chief Executive Officer of X-Therma

“This submission was the culmination of several years of development activities and the establishment of a Good Manufacturing Practices (GMP) manufacturing facility in Hercules, California. We are poised to provide worldwide supply of this next-generation product intended for use within the biologics, gene therapy, tissue engineering, and cell therapy sectors.”

X-Therma submitted the DMF to the FDA in January 2024, and the FDA accepted it on January 31, 2024. X-Therma clients who use the product to preserve therapeutic cells will be able to reference the DMF in their Investigational New Drug (IND) and Biologics License Application (BLA) submissions to the FDA for products in the Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER).

XT-Thrive® is a DMSO-free, serum-free, protein-free, and chemically defined cryopreservation media enabling the preservation of mammalian cells at ultra-low temperatures (-70° C to -196° C). It incorporates a fundamentally new class of cryoprotectant, named peptoids, fully synthetic defined molecules are inspired by natural antifreeze proteins (hyper-effective and non-toxic) to prevent aberrant ice formation and risk of shock-induced ice damage. This product can be used for the cryopreservation of cells used for manufacture of biological products including monoclonal antibodies, recombinant proteins, fusion proteins, and vaccines. XT-Thrive® does not require a manual wash-out step, thus elevating its safety profile in comparison to other cryopreservation media.

Michael Osborne, MBA, SVP of Commercialization at X-Therma Added

“XT-Thrive® is tailored to provide high cell recovery and functionality that poses many advantages over other products on the market. It is the plug-and-play solution for cell and tissue manufacturing processes to enable greater bioproduction scale-up, reliability, and consistency.”

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Recent News

How Nefab’s Sustainable Packaging and Logistics Solutions Revolutionize the Healthcare Equipment Industry Supply Chain | By Lise-Anais Swiegot, Global Healthcare Segment Director with the Nefab Group

For over 75 years, Nefab has been a global industrial packaging provider, delivering tailored transportation and logistics solutions to customers in 38 countries. Originating from Sweden, Nefab has expanded to employ over 4,700 individuals, including more than 250 engineers worldwide.

Discover Reeva FT: Revolutionizing Wound Covering for Healthcare Pros

Reeva FT is offered in a variety of sizes: 2x2 cm, 2x3 cm, 4x4 cm, 4x6 cm, 4x8 cm, and 10x15 cm. Reeva FT is confirmed by the FDA Tissue Reference Group to meet the criteria for regulation solely under Section 361 of the PHS Act as defined in 21 CFR Part 1271.

Medical Grade, Premium Standing Solutions Drastically Improve Employee Comfort, Support, Productivity and Morale While Reducing Fatigue, Stress and Ailments | By Amy Hester, PhD, RN, BC, FAAN, Chairwoman and CEO, HD Nursing, & Daniel Bouzide, Founder and President, WellnessMats

A significant review found that a staggering 77.2% of nurses experience Work-Related Musculoskeletal Disorders within a year. This high incidence rate highlights the physical strain of nursing duties, which often include extended periods of standing, and underscores the need for effective interventions.
Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Stay Connected

spot_img
spot_img

By using this website you agree to accept Medical Device News Magazine Privacy Policy