Innovative Embolic Device Shows Promise for Interventional Oncology Drug Delivery

Fluidx Medical’s GPX Embolic Device Releases Initial Results for Oncology Drug Delivery

Fluidx Medical Technology announced that a next-generation, doxorubicin-loaded GPX Embolic Device was featured at the recent Symposium on Clinical Interventional Oncology (CIO) Conference highlighting the technology’s potential for oncology drug delivery.

“GPX is easy to prepare, deliver, and control,” said Ryan O’Hara, M.D., Interventional Oncologist, University of Utah, Salt Lake City, Utah.  “The initial results of GPX as a drug-loadable oncology solution are very promising.  GPX would be the first loadable liquid embolic designed for tumor applications.”

Study results presented at CIO included an in vitro characterization of the loading and drug release profile of the GPX Embolic Material loaded with doxorubicin (GPX-DOX).  GPX-DOX provided a zero-order release profile for 5 weeks and sustained release out to 100 days.  The long linear release profile is desirable in drug delivery, as a constant amount of drug is delivered regardless of the concentration within the carrier. These properties are unique in the field of liquid embolics.

Innovative Embolic Device Shows Promise for Interventional Oncology Drug Delivery News

The GPX Embolic Device is an innovative embolic designed for simple preparation and quick material delivery.  GPX technology is a low viscosity, aqueous-based solution in a syringe that solidifies into a durable embolus upon delivery without polymerization or dimethyl-sulfoxide (DMSO) precipitation.  GPX is designed to occlude blood vessels independent of a patient’s coagulation situation.  The device is packaged ready-to-use in a syringe, requires less than 30 seconds of tableside preparation by the clinician, and may be delivered through standard catheters or small microcatheters (no complex mixing systems or special delivery catheters are necessary). *

“We have not seen other liquid embolic devices that have demonstrated the ability to load and release oncology agents in a sustained manner,” said Libble Ginster, CEO of Fluidx Medical Technology.  “The Fluidx team is excited about the future of GPX technology and inspired by bringing new innovations to cancer patient care.”

Fluidx Medical Technology is a Salt Lake City, Utah-based company focused on developing the GPX Embolic Device and other innovative medical technologies.

The GPX Embolic Device is under development and does not have marketing clearance or approval in any market at this time. For investigational use (in New Zealand) only.  GPX-DOX Embolic Device is under development and does not have marketing clearance or approval in any market at this time.

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.”