Theradaptive Awarded Manufacturing Assistance Grant by the Maryland Stem Cell Research Fund

Today, Theradaptive a biopharmaceutical firm pioneering advancements in targeted regenerative therapeutics, has been awarded the Manufacturing Assistance Program grant by the Maryland Stem Cell Research Fund (MSCRF). The grant will help Theradaptive develop their GMP Manufacturing Facility in Frederick, stimulating economic development in the state and bolstering Maryland’s reputation as a hub of biotechnological innovation.

Theradaptive seeks to significantly improve patient outcomes by producing targeted therapeutics that can be used to coat implants, devices, and injectable carriers. Their proprietary protein-engineering platform aims to provide greater efficacy, safety, and ease of use across multiple clinical indications including orthopedics, immuno-oncology and dental.

To date, the MSCRF has invested over $177 million in the pursuit of accelerated stem cell research, cures, and commercialization. Their Manufacturing Assistance Program grant will support Theradaptive in increasing the production of their OsteoAdapt regenerative therapeutic product for spine and trauma repair in preparation for first-in-human clinical trials.

Kevin Anderson, Secretary of Commerce at the Maryland Department of Commerce comments on the award: “Maryland Commerce is thrilled to support Theradaptive, an ambitious and innovative company whose new facility will help drive economic development and enhance our state’s reputation as a leading biotechnology hub. As Theradaptive approaches human trials, this new funding will create jobs and help set Maryland apart as one of the most attractive biotech investment areas in the US.”

Ruchika Nijhara, Executive Director at the Maryland Stem Cell Research Fund (MSCRF) states: “The recent award of a Manufacturing Assistance Program grant to Theradaptive represents MSCRF’s commitment to fostering the growth of Maryland cell-based therapy companies and facilitating the establishment of biomanufacturing capabilities within the state. We are excited to witness the development and expansion of their GMP OsteoAdapt Manufacturing Facility in Maryland, which will play a pivotal role in increasing the production of their orthopedic product. Through this growth, we anticipate a positive impact on patient outcomes, benefiting millions of individuals in need.”

Ed Fix, Vice President of Manufacturing at Theradaptive adds: “We are deeply honored to be awarded a Manufacturing Support Award by MSCRF. This award will enable us to establish our own cGMP manufacturing capabilities at our Frederick headquarters and allow us to tap into the rich pipeline of talent in the Maryland area. Manufacturing will be a critical piece in our journey to bring life changing therapies to patients.”

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”
Exit mobile version