Xeris secures patent protection for Keveyis through 2039
Xeris Pharmaceuticals, Inc., a wholly owned subsidiary of Biopharma Holdings, Inc., received a Notice of Allowance from the USPTO for U.S. Patent Application No. 17/151,405, covering KEVEYIS. The patent is expected to provide protection through 2039, pending administrative steps. The company plans to submit the patent to the FDA for Orange Book listing.

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Xeris Pharmaceuticals, Inc., a wholly owned subsidiary of Biopharma Holdings, Inc. (NASDAQ: XERS), announced that the United States Patent and Trademark Office (USPTO) has issued a Notice of Allowance for a new patent covering its KEVEYIS (dichlorphenamide) product. The allowed claims in U.S. Patent Application No. 17/151,405, entitled "Compositions and Methods of Use," cover the use of KEVEYIS. This development is expected to provide intellectual property protection for the therapy through 2039, reinforcing the company's commitment to the primary periodic paralysis community.
The Notice of Allowance indicates that the USPTO has determined the application meets the requirements for patentability. Following the completion of standard administrative steps and the payment of maintenance fees, the patent is expected to issue as a U.S. patent. Xeris intends to submit the patent to the U.S. Food and Drug Administration (FDA) for listing in the Orange Book, a publication of approved drug products with therapeutic equivalence evaluations.
KEVEYIS is an FDA-approved treatment for primary periodic paralysis (PPP), including primary hyperkalemic periodic paralysis, primary hypokalemic periodic paralysis, and related variants. PPP is a rare genetic condition characterized by episodes of muscle weakness or temporary paralysis. The therapy has been shown to reduce the number, severity, and duration of PPP attacks.
Key Details of the Patent Allowance
| Detail | Description |
|---|---|
| Patent Application No. | 17/151,405 |
| Title | Compositions and Methods of Use |
| Product Covered | KEVEYIS (dichlorphenamide) |
| Expected Protection Term | Through 2039 |
| Next Step | Submission to FDA for Orange Book listing |
John Shannon, CEO of Xeris, stated that the Notice of Allowance reflects the company's long-standing commitment to the patient community that depends on KEVEYIS. He emphasized that strengthening the intellectual property around the therapy ensures the company can continue to deliver this treatment and support the primary periodic paralysis community.
Xeris Biopharma Holdings is a biopharmaceutical company focused on developing and commercializing innovative products across various therapies. In addition to KEVEYIS, its commercial products include RECORLEV for endogenous Cushing's syndrome and GVOKE for severe hypoglycemia.
How will the extended patent protection through 2039 impact Xeris's revenue projections and pricing strategy for KEVEYIS?
What are the potential risks of generic competition or patent challenges before the 2039 expiration date?
Could this patent allowance pave the way for Xeris to expand KEVEYIS into new markets or therapeutic indications?

























