NRx Pharmaceuticals Announces Close of $2.9 Million Registered Direct Offering
Rhea-AI Summary
NRx Pharmaceuticals has successfully completed a registered direct offering, raising approximately
Positive
- Raised $2.9 million to support NRX-101 development.
- Funds will help initiate a National Treatment Protocol and Safety Database.
- Investor confidence highlighted by participation of existing investors.
Negative
- The offering may dilute existing shareholders' equity.
News Market Reaction 1 Alert
On the day this news was published, NRXP declined 1.39%, reflecting a mild negative market reaction.
Data tracked by StockTitan Argus on the day of publication.
NRx Pharmaceuticals received approximately in cash from existing investors.$2.9 million - Offering will assist the Company to initiate its National Treatment Protocol and Safety Database for NRX-101 for Treatment-Resistant Bipolar Depression with Risk of Self Harm.
The gross proceeds from the offering are expected to be approximately
The securities in the offering described above are being offered by the Company pursuant to a registration statement on Form S-3 (File No. 333-265492) that was filed with the
This press release does not constitute an offer to sell or the solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under securities laws of any such jurisdiction.
About
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.
Cautionary Note Regarding Forward-Looking Statements
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.
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