NeuroBo Pharmaceuticals Announces up to $70 Million Concurrent Private Placement and Registered Direct Offering Priced At-the-Market Under Nasdaq Rules
NeuroBo Pharmaceuticals (Nasdaq: NRBO) has announced two concurrent financial events: a private placement and a registered direct offering, both priced at-the-market under Nasdaq rules. The company aims to secure $20 million initially, with potential additional gross proceeds of up to $50 million through the exercise of Series Warrants. The funds will support the Phase 1 Part 3 clinical trial for DA-1726, targeting obesity treatment.
The private placement involves selling 4,325,701 shares at $3.93 per share, while the direct offering includes 763,359 shares at the same price. Unregistered Series A and B warrants will be issued for the purchase of up to 12,722,651 shares in total, with varying expiration conditions based on clinical milestones.
The closing is expected around June 25, 2024, pending customary conditions. H.C. Wainwright & Co. is the exclusive placement agent. The proceeds will be used for working capital, general corporate purposes, and continued clinical development of DA-1726.
- Potential to raise up to $70 million in total funding.
- Initial $20 million secured for immediate financial needs and trial support.
- Funds allocated to complete Phase 1 Part 3 clinical trial for DA-1726.
- No assurance given on the exercise of Series Warrants.
- Dependence on clinical milestone achievements for additional funding.
Insights
The announcement from NeuroBo Pharmaceuticals represents a significant capital infusion aimed at advancing their clinical trials. For investors, the initial
The pricing at
From a financial standpoint, the immediate and potentially future funds are vital for NeuroBo's operational sustainability. However, the successful advancement of their clinical trials will be a key determinant of the company's financial health and stock performance.
The focus of the investment on DA-1726, aimed at treating obesity, is particularly notable. Obesity is a major health issue with significant unmet needs, making it a lucrative market if the clinical trials are successful. The structured nature of the Series A and B warrants ties the potential additional funding directly to positive clinical milestones, which is a strategic move. This not only provides a financial incentive to investors but also demonstrates the company's confidence in their clinical progress.
Phase 1 trials are important in determining the safety and initial efficacy of DA-1726. The structure of the warrants suggests that NeuroBo is expecting significant positive data readouts in the near term, first from the Multiple Ascending Dose (MAD) study and later from the Phase 1 Part 3 study. Investors should monitor these milestones closely as they will have direct implications on the additional capital inflow and, consequently, the continuation of the drug's development.
The potential success of the Phase 1 trials could also enhance NeuroBo's standing and attract more significant investment or partnership opportunities, leveraging their position in the competitive biotech landscape.
H.C. Wainwright & Co. is acting as the exclusive placement agent for the offerings.
The aggregate gross proceeds to NeuroBo from the offerings are expected to be approximately
The shares of common stock offered in the registered direct offering (but excluding the securities offered in the private placement and the shares of common stock underlying the warrants issued in the private placement) are being offered and sold by NeuroBo pursuant to a "shelf" registration statement on Form S-3 (Registration No. 333-278646), including a base prospectus, previously filed with the Securities and Exchange Commission ("SEC") on April 12, 2024 and declared effective by the SEC on April 23, 2024. The offering of the shares of common stock to be issued in the registered direct offering are being made only by means of a prospectus supplement that forms a part of the registration statement. A final prospectus supplement and an accompanying base prospectus relating to the registered direct offering will be filed with the SEC and will be available on the SEC's website located at http://www.sec.gov. Electronic copies of the final prospectus supplement and the accompanying base prospectus, when available, may be obtained on the SEC's website at http://www.sec.gov and may also be obtained, when available, by contacting H.C. Wainwright & Co., LLC at 430 Park Avenue, 3rd Floor,
The offer and sale of the securities in the private placement and the Series Warrants described above are being made in a transaction not involving a public offering and have not been registered under Section 4(a)(2) of the Securities Act of 1933, as amended (the "Securities Act") and/or Rule 506(b) of Regulation D promulgated thereunder and, along with the shares of common stock underlying the warrants issued in the private placement, have not been registered under the Securities Act or applicable state securities laws. Accordingly, the securities in the private placement, the Series Warrants and underlying shares of common stock may not be offered or sold in the United States except pursuant to an effective registration statement with the SEC or an applicable exemption from the registration requirements of the Securities Act and such applicable state securities laws. NeuroBo has agreed to file an initial registration statement with the SEC covering the resale of the securities to be issued in the private placement.
This press release shall not constitute an offer to sell or a solicitation of an offer to buy any of the securities described herein, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.
About NeuroBo Pharmaceuticals
NeuroBo Pharmaceuticals, Inc. is a clinical-stage biotechnology company focused on transforming cardiometabolic diseases. The company is currently developing DA-1726 for the treatment of obesity, and is developing DA-1241 for the treatment of Metabolic Dysfunction-Associated Steatohepatitis (MASH). DA-1726 is a novel oxyntomodulin (OXM) analogue that functions as a glucagon-like peptide-1 receptor (GLP1R) and glucagon receptor (GCGR) dual agonist. OXM is a naturally-occurring gut hormone that activates GLP1R and GCGR, thereby decreasing food intake while increasing energy expenditure, thus potentially resulting in superior body weight loss compared to selective GLP1R agonists. DA-1241 is a novel G-protein-coupled receptor 119 (GPR119) agonist that promotes the release of key gut peptides GLP-1, GIP, and PYY. In pre-clinical studies, DA-1241 demonstrated a positive effect on liver inflammation, lipid metabolism, weight loss, and glucose metabolism, reducing hepatic steatosis, hepatic inflammation, and liver fibrosis, while also improving glucose control.
For more information, please visit www.neurobopharma.com.
Forward Looking Statements
Certain statements in this press release may be considered forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as "believes", "expects", "anticipates", "may", "will", "should", "seeks", "approximately", "intends", "projects", "plans", "estimates" or the negative of these words or other comparable terminology (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements, which include, among other statements, statements regarding the completion of the offerings, the satisfaction of customary closing conditions related to the offerings, the anticipated use of proceeds therefrom, the ability of NeuroBo to achieve certain milestone events; the exercise of the Series Warrants upon the achievement of such milestone events or otherwise prior to their expiration and the receipt of stockholder approval. Forward-looking statements are predictions, projections and other statements about future events that are based on current expectations and assumptions and, as a result, are subject to risks and uncertainties. Many factors could cause actual future events to differ materially from the forward-looking statements in this press release, including, without limitation, market and other conditions, those risks associated with NeuroBo's ability to execute on its commercial strategy; the timeline for regulatory submissions; ability to obtain regulatory approval through the development steps of NeuroBo's current and future product candidates, the ability to realize the benefits of the license agreement with Dong-A ST Co. Ltd., including the impact on future financial and operating results of NeuroBo; the cooperation of NeuroBo's contract manufacturers, clinical study partners and others involved in the development of NeuroBo's current and future product candidates; potential negative interactions between NeuroBo's product candidates and any other products with which they are combined for treatment; NeuroBo's ability to initiate and complete clinical trials on a timely basis; NeuroBo's ability to recruit subjects for its clinical trials; whether NeuroBo receives results from NeuroBo's clinical trials that are consistent with the results of pre-clinical and previous clinical trials; impact of costs related to the license agreement, known and unknown, including costs of any litigation or regulatory actions relating to the license agreement; effects of changes in applicable laws or regulations; effects of changes to NeuroBo's stock price on the terms of the license agreement and any future fundraising; and other risks and uncertainties described in NeuroBo's filings with the Securities and Exchange Commission, including NeuroBo's most recent Annual Report on Form 10-K. Forward-looking statements speak only as of the date when made. NeuroBo does not assume any obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.
Contacts:
NeuroBo Pharmaceuticals
Marshall H. Woodworth
Chief Financial Officer
+1-857-299-1033
marshall.woodworth@neurobopharma.com
Rx Communications Group
Michael Miller
+1-917-633-6086
mmiller@rxir.com
SOURCE NeuroBo Pharmaceuticals, Inc.
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