Portal Diabetes Gets FDA Breakthrough for Pump, Starts Insulin Study
Two steps toward bringing a functional cure to T1D
The
The Breakthrough Device Designation will facilitate priority interactions with the FDA as Portal plans clinical trials and navigates regulatory approvals, and the designation establishes eligibility for the Transitional Coverage for Emerging Technologies (TCET) pathway, expediting Medicare coverage for FDA-designated breakthrough devices. Under an Investigational New Drug application, the first two patients recently received Portal Insulin by injection into the intraperitoneal space at a clinical site in
"We believe patients will achieve much better glycemic control for a dramatically reduced mental burden with the Portal Pump," expressed
Clinical trials on the combination system are planned to begin around Q4 2027. Endocrinologists, surgeons, and their clinical sites interested in participating may contact the Company to express their interest.
The Portal Pump is not available for sale or investigational use in
Media Contact: Company Contact: [email protected]
About Portal Diabetes
Portal Diabetes is developing an implantable insulin pump system and a concentrated, stable insulin. With the physiologic delivery of insulin to the abdomen integrated with modern iCGM technology, the Portal Pump with Portal Insulin stands to fully close the insulin delivery loop to improve patient well-being. To learn more about how Portal Diabetes is disrupting diabetes care, visit www.portaldiabetes.com.
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SOURCE Portal Diabetes, Inc.
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