NRx Pharmaceuticals Builds on Its Intellectual Property Foundation for Neuropsychiatric Conditions - Adds New U.S. Patent to Portfolio
NRx Pharmaceuticals has announced the issuance of a new U.S. patent covering its lead product candidate, NRX-101, a treatment for bipolar depression and suicidality. This patent, part of the company’s third patent family, brings its total to 48 issued patents worldwide, with 42 pending. The patent secures NRX-101’s use in treating major depression and bipolar disorder until at least 2033. The drug, currently in clinical trials, has received FDA Breakthrough Therapy Designation. Upon approval, the patent is expected to be eligible for listing in the FDA's Orange Book.
- Issuance of U.S. Patent No. 11,576,911 strengthens NRX Pharmaceuticals' intellectual property portfolio.
- Total of 48 issued patents globally enhances the company's competitive position.
- Patent coverage extends until at least 2033, protecting NRX-101's formulation and uses.
- None.
- Company receives notice of the issuance of a
U.S. patent covering the lead formulation, NRX-101, a glycine site NMDA antagonist in clinical trials to treat bipolar depression with acute and subacute suicidality; - This new patent represents a third patent family, that now totals 48 issued patents worldwide with 42 additional pending patent applications.
- Patent covers the use of NRX-101 to treat patients suffering from depression, including bipolar depression or major depression (MDD) with or without suicidality and strengthens the Company's intellectual property position until at least 2033;
- Upon approval of NRX-101, this newly granted patent is expected to be "listable" in the
U.S. Food and Drug Administration (FDA) Orange Book.
This patent, issued to
In particular, the claims of the new patent cover methods for treating a patient suffering from depression, including bipolar depression or major depression, with or without suicidality by administering to the patient an effective amount of the Company's lead product candidate, NRX-101. Should this drug candidate be approved by the
"The grant of this new patent augments the strength of
In 2023, the company expects to have additional patents granted from its pending portfolio and to file more patent applications in the
Up to
Conventional antidepressants can increase the risk of suicide in certain patients; hence their labels contain a warning to that effect. NRX-101 is a patented, oral, fixed dose combination of D-cycloserine and lurasidone, neither of which has shown addiction potential in preclinical models. Based on the results of a Phase 2 proof-of-concept study, NRX-101 received Breakthrough Therapy Designation from the FDA for the treatment of severe bipolar depression in patients with ASIB after initial stabilization with ketamine or other effective therapy.
NRX-101 is one of the first oral antidepressants currently in late-stage clinical studies targeting the NMDA-receptor in the brain, which represents potentially a key new mechanism to treat depression with and without suicidality, as well as PTSD and other indications. To date, NRX-101 is the only oral NMDA investigational medicine focused on bipolar depression in patients with acute and sub-acute suicidality.
Clinical-stage biopharmaceutical company developing therapeutics for the treatment of central nervous system disorders, specifically suicidal depression and post-traumatic stress disorder (PTSD). The company's lead program NRX-101, an oral, fixed-dose combination of D-cycloserine and lurasidone, targets the brain's NMDA receptor and is being investigated in a Phase 3 trial under an FDA Special Protocol Agreement and Breakthrough Therapy Designation in patients with bipolar depression and suicidal ideation, an indication for which the only approved treatment is electroshock therapy. NRx Pharmaceuticals has also initiated a Phase 2b clinical trial in patients with Sub-Acute Suicidality, a substantially broader indication. The Breakthrough Therapy Designation and Special Protocol Agreement were awarded by the FDA based on the Company's prior STABIL-B trial that demonstrated substantial improvement over available therapy in reducing depression and suicidality compared to placebo when patients were treated with NRX-101 after a single dose of ketamine.
This announcement of
The Company assumes no obligation to revise any forward-looking statement, whether as a result of new information, future events or otherwise. Accordingly, you should not place reliance on any forward-looking statement, and all forward-looking statements are herein qualified by reference to the cautionary statements set forth above.
CORPORATE CONTACT
Sr. Director,
mcogan@nrxpharma.com
INVESTOR RELATIONS
Investor Relations
suzanne.messere@sternir.com
View original content to download multimedia:https://www.prnewswire.com/news-releases/nrx-pharmaceuticals-builds-on-its-intellectual-property-foundation-for-neuropsychiatric-conditions---adds-new-us-patent-to-portfolio-301752767.html
SOURCE
FAQ
What is the significance of the new U.S. patent for NRX Pharmaceuticals (NRXP)?
When does the patent for NRX-101 expire?
How many patents does NRX Pharmaceuticals currently hold?
What is NRX-101 used to treat?