Welcome to our dedicated page for Nrx Pharmaceuticals news (Ticker: NRXP), a resource for investors and traders seeking the latest updates and insights on Nrx Pharmaceuticals stock.
NRx Pharmaceuticals, Inc. (NASDAQ: NRXP) is a clinical-stage biopharmaceutical company whose news flow centers on its NMDA-based drug pipeline and interventional psychiatry operations. Company announcements frequently highlight progress with NRX-100, a preservative-free intravenous ketamine formulation, and NRX-101, an oral D-cycloserine/lurasidone combination, both aimed at serious central nervous system disorders such as suicidal depression and suicidal bipolar depression.
Investors following NRXP news can expect updates on FDA interactions, including Fast Track and Breakthrough Therapy designations, Abbreviated New Drug Application (ANDA) milestones for preservative-free ketamine, and New Drug Application (NDA) activities. The company also reports on the use of large Real World Evidence datasets to support potential Accelerated Approval pathways for NRX-100 in suicidal ideation associated with depression and bipolar depression.
Another recurring theme in NRx Pharmaceuticals’ news is the expansion of its HOPE Therapeutics subsidiary, which operates interventional psychiatry clinics. Releases describe clinic acquisitions, strategic interests in practices, and deployment of treatments such as ketamine-based therapies, Transcranial Magnetic Stimulation (TMS), Hyperbaric Oxygen Therapy, and digital therapeutics for suicidal depression, PTSD, and related conditions. Updates often cover new treatment protocols that combine TMS with D-cycloserine and other medications.
NRXP news items also include corporate developments such as conference presentations, corporate update calls, financing transactions, and changes in independent registered public accounting firms, as reflected in SEC filings. For investors and observers, the news stream provides ongoing insight into NRx Pharmaceuticals’ clinical progress, regulatory steps, clinic network growth, and capital markets activity related to its focus on Neuroplastic Therapies and suicidal depression.
NRx Pharmaceuticals (NASDAQ:NRXP), a clinical-stage biopharmaceutical company, announced its selection to present at the Wall Street Conference on May 21, 2025 in Palm Beach, Florida. Dr. Jonathan Javitt, Founder, Chairman and CEO of NRx and Co-CEO of HOPE Therapeutics, will provide a company update focusing on progress towards FDA approval of NRX-100 (preservative-free ketamine) and upcoming acquisitions of HOPE clinics specializing in treatment of suicidal depression, PTSD, and related disorders.
The conference, which will host six presenting companies, is expected to attract over 1,000 attendees representing more than $1 trillion in investment capital.
HOPE Therapeutics, a subsidiary of NRx Pharmaceuticals (NASDAQ:NRXP), has secured a term sheet with Universal Capital for $7.8 million in debt financing. Combined with a previously announced strategic investment, HOPE is set to receive $10.3 million in total acquisition capital.
The funding will support HOPE's national expansion strategy through the acquisition of interventional psychiatry clinics, starting with Dura Medical, Kadima, and NeuroSpa. These clinics specialize in neuroplastic treatments, including ketamine and transcranial magnetic stimulation (TMS), for treating severe depression, PTSD, and related conditions. The clinics currently serve veterans through Veterans Health Administration contracts and the general public.
Universal Capital shares HOPE's vision of establishing a nationwide network of mental health clinics and plans to participate in future funding as additional acquisitions are identified.HOPE Therapeutics, a subsidiary of NRx Pharmaceuticals (NASDAQ:NRXP), has signed a definitive agreement to acquire Kadima Neuropsychiatry Institute in La Jolla, CA. Kadima, a profitable clinic specializing in interventional psychiatry, will serve as the clinical model for HOPE's nationwide treatment network. The institute is a leading research site for CNS and psychedelic therapies, offering treatments including ketamine, Spravato, and TMS for conditions like suicidal depression and PTSD.
Dr. David Feifel, Kadima's founder and a recognized expert in interventional psychiatry, will join HOPE as Chief Medical Innovation Officer post-acquisition. The acquisition is expected to be accretive to revenue and EBITDA for both NRx and HOPE, subject to closing conditions and financing finalization.
NRx Pharmaceuticals (NASDAQ: NRXP), a clinical-stage biopharmaceutical company, has scheduled its first quarter 2025 financial results announcement for May 15, 2025, after market close. The company will release results through a press release available on their investor relations website, followed by a conference call at 4:30 PM ET.
Interested parties can access the conference call via webcast on the company's website or by telephone using the following dial-in numbers: +1-800-717-1738 (domestic) or +1-646-307-1865 (international).
NRx Pharmaceuticals (NASDAQ:NRXP) and its subsidiary HOPE Therapeutics announced an upcoming investor event at Mar-A-Lago Club on May 8, 2025. The event will discuss strategic initiatives including HOPE's interventional psychiatry clinic expansion and NRx's clinical pipeline progress.
Key discussion topics include: HOPE's recent clinic acquisitions, integration of digital health solutions, status of NRX-100 (preservative-free IV Ketamine) NDA following a $4.3M FDA filing fee waiver, a new patent filing for NRX-100 that could provide market exclusivity until 2045, and the Breakthrough Therapy Designation of NRX-101 for bipolar depression treatment. Dr. Jonathan Javitt, Chairman and CEO of NRx and Co-CEO of HOPE Therapeutics, will lead the discussion.
NRx Pharmaceuticals (NASDAQ:NRXP) has filed a patent application for NRX-100, its preservative-free intravenous ketamine formulation designed to treat suicidal depression. The patent, if granted, would provide exclusivity until 2045 and could be listed in the FDA Orange Book. NRX-100's key innovation is its formulation without benzethonium chloride or other preservatives, which have been linked to cytotoxic or neurotoxic effects.
The company has already initiated an NDA filing for NRX-100 and received Fast Track Designation with NRX-101 from the FDA. With a recent FDA fee waiver in place, NRx plans to complete its NDA submission in the current quarter. The patent application includes twenty claims covering pharmaceutical compositions, treatment methods, and manufacturing processes.