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# Breakthrough Designation for Immunicom Cancer Device
- URL: https://www.fdaweb.com/breakthrough-designation-for-immunicom-cancer-device/
- Published: 2018-05-14T12:00:00.000Z
- Updated: 2026-09-15T00:04:54.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141432

FDA has granted Immunicom a breakthrough device designation for its Immunopheresis therapy, which is based on a proprietary technology that selectively removes immune inhibitors from patients’ bloodstreams and thus enables their natural immune system to more-effectively attack cancer tumors. “By removing immune system inhibitors from the blood without introducing new substances, Immunicom’s therapeutic approach has been shown in preliminary preclinical studies to enhance anti-cancer immune system response without causing unwanted side effects,” the company says.

Immunopheresis is a blood fractionation methodology to remove specific blood components to stimulate a natural immune response. “The significant advantage of Immunopheresis over all non ‘pheresis’ types of immune therapy is that nothing is put into the patient and the materials removed are only a small portion of the patient’s total blood content,” the company says.