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REGENXBIO Announces Pricing of Upsized Public Offering of Common Stock and Pre-funded Warrants

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REGENXBIO Inc. announces the pricing of an underwritten upsized public offering, expecting to raise approximately $140.0 million. The offering includes 4,565,260 shares of common stock and 1,521,740 pre-funded warrants. The company has granted the underwriters an option to purchase an additional 913,050 shares. The offering is expected to close on March 11, 2024.
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The recent public offering by REGENXBIO Inc. represents a significant influx of capital, anticipated to be around $140 million. This capital injection is critical for a clinical-stage biotech company, as it provides the necessary funds to continue research and development, particularly in the expensive field of gene therapy. The pricing of the shares and pre-funded warrants suggests a strategic move to attract investment without a substantial discount, which could potentially maintain shareholder value while still expanding the capital base.

Investors should note the involvement of high-profile financial institutions such as Morgan Stanley and Goldman Sachs, which often indicates confidence in the offering's success. The 30-day option for underwriters to purchase additional shares provides a buffer that could lead to further capital if the offering is well-received, indicating potential for stock price stabilization post-offering.

REGENXBIO's focus on gene therapy is situated in a high-growth potential market but comes with considerable risk due to the complex nature of clinical trials and regulatory approvals. The capital raised could accelerate the company's pipeline projects towards commercialization, which is a critical factor for long-term success in the biotech industry. However, the dilutive effect of increasing the number of shares could be a concern for existing shareholders, as it may affect earnings per share.

Market trends show that biotech firms with innovative platforms and a robust pipeline are attractive for long-term investment, despite the inherent risks. The timing and pricing of this offering may reflect the company's strategic positioning and confidence in its technology, which could be a positive signal for investors looking at the growth prospects of the gene therapy sector.

REGENXBIO's offering is conducted under a shelf registration statement, which allows the company to prepare the offering documents ahead of time and go to market quickly when conditions are favorable. This method is often used by companies to have flexibility in timing the market and ensuring capital is raised efficiently. The fact that the offering is upsized suggests strong investor interest or a greater need for funds than initially anticipated.

It's important to note that the offering's successful closure is subject to customary closing conditions and regulatory compliance. The company's adherence to SEC regulations, including the filing of a preliminary prospectus supplement, is crucial in maintaining transparency with investors and avoiding legal complications that could arise from securities offerings.

ROCKVILLE, Md., March 6, 2024 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) a leading clinical-stage biotechnology company seeking to improve lives through the curative potential of gene therapy, today announced the pricing of an underwritten upsized public offering of 4,565,260 shares of its common stock at the price of $23.00 per share and 1,521,740 pre-funded warrants at a price of $22.9999 per warrant, in each case before underwriting discounts and commissions. The gross proceeds to REGENXBIO from the offering, before deducting the underwriting discounts and commissions and other offering expenses payable by REGENXBIO, are expected to be approximately $140.0 million. This offering is expected to close on March 11, 2024, subject to customary closing conditions. In addition, REGENXBIO has granted the underwriters a 30-day option to purchase an additional 913,050 shares of common stock at the public offering price, less underwriting discounts and commissions.

Morgan Stanley, Goldman Sachs & Co. LLC, Barclays and Stifel are acting as joint book-running managers of the offering.

The securities described above are being offered by REGENXBIO pursuant to a shelf registration statement on Form S-3 that was filed with the Securities and Exchange Commission (the "SEC") on December 30, 2022 (File No. 333-269086) and became automatically effective upon filing. A preliminary prospectus supplement relating to and describing the terms of the offering was filed with the SEC and is available on the SEC's website at www.sec.gov. Copies of the preliminary prospectus supplement and the accompanying prospectus relating to this offering, when available, may be obtained from: Morgan Stanley & Co. LLC, Attention: Prospectus Department, 180 Varick Street, 2nd Floor, New York, NY 10014, or by email at prospectus@morganstanley.com; Goldman Sachs & Co. LLC, Attention: Prospectus Department, 200 West Street, New York, NY 10282, by phone at (866) 471-2526, or by email at prospectus-ny@ny.email.gs.com; Barclays Capital Inc., c/o Broadridge Financial Solutions, at 1155 Long Island Avenue, Edgewood, New York 11717 or by email at barclaysprospectus@broadridge.com; or Stifel, Nicolaus & Company, Incorporated, Attention: Prospectus Department, One Montgomery Street, Suite 3700, San Francisco, CA 94104, by telephone at (415) 364-2720 or by email at syndprospectus@stifel.com. The final terms of the offering will be disclosed in a final prospectus supplement to be filed with the SEC.

This press release shall not constitute an offer to sell or a solicitation of an offer to buy any of these securities, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the applicable securities laws of such state or jurisdiction.

ABOUT REGENXBIO Inc.

REGENXBIO is a leading clinical-stage biotechnology company seeking to improve lives through the curative potential of gene therapy. Since its founding in 2009, REGENXBIO has pioneered the development of AAV Therapeutics, an innovative class of gene therapy medicines. REGENXBIO is advancing a pipeline of AAV Therapeutics for retinal and rare diseases, including ABBV-RGX-314 for the treatment of wet AMD and diabetic retinopathy, being developed in collaboration with AbbVie, RGX-202 for the treatment of Duchenne and RGX-121 for the treatment of MPS II. Thousands of patients have been treated with REGENXBIO's AAV Therapeutic platform, including Novartis' ZOLGENSMA for children with spinal muscular atrophy. Designed to be one-time treatments, AAV Therapeutics have the potential to change the way healthcare is delivered for millions of people.

FORWARD-LOOKING STATEMENTS

This press release includes "forward-looking statements," within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements express a belief, expectation or intention and are generally accompanied by words that convey projected future events or outcomes such as "believe," "may," "will," "estimate," "continue," "anticipate," "assume," "design," "intend," "expect," "could," "plan," "potential," "predict," "seek," "should," "would" or by variations of such words or by similar expressions. The forward-looking statements include statements relating to, among other things, statements regarding the timing and success of the proposed offering and whether REGENXBIO will be able to raise capital through the sale of shares of common stock and pre-funded warrants in the offering. REGENXBIO has based these forward-looking statements on its current expectations and assumptions and analyses made by REGENXBIO in light of its experience and its perception of historical trends, current conditions and expected future developments, as well as other factors REGENXBIO believes are appropriate under the circumstances. However, whether actual results and developments will conform with REGENXBIO's expectations and predictions is subject to a number of risks and uncertainties, including the timing of enrollment, commencement and completion and the success of clinical trials conducted by REGENXBIO, its licensees and its partners, the timing of commencement and completion and the success of preclinical studies conducted by REGENXBIO and its development partners, the timely development and launch of new products, the ability to obtain and maintain regulatory approval of product candidates, the ability to obtain and maintain intellectual property protection for product candidates and technology, trends and challenges in the business and markets in which REGENXBIO operates, the size and growth of potential markets for product candidates and the ability to serve those markets, the rate and degree of acceptance of product candidates, and other factors, many of which are beyond the control of REGENXBIO. Refer to the "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" sections of REGENXBIO's Annual Report on Form 10-K for the year ended December 31, 2023, and comparable "risk factors" sections of REGENXBIO's Quarterly Reports on Form 10-Q and other filings, which have been filed with the U.S. Securities and Exchange Commission (SEC) and are available on the SEC's website at www.sec.gov. All of the forward-looking statements made in this press release are expressly qualified by the cautionary statements contained or referred to herein. The actual results or developments anticipated may not be realized or, even if substantially realized, they may not have the expected consequences to or effects on REGENXBIO or its businesses or operations. Such statements are not guarantees of future performance and actual results or developments may differ materially from those projected in the forward-looking statements. Readers are cautioned not to rely too heavily on the forward-looking statements contained in this press release. These forward-looking statements speak only as of the date of this press release. Except as required by law, REGENXBIO does not undertake any obligation, and specifically declines any obligation, to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

Zolgensma® is a registered trademark of Novartis Gene Therapies. All other trademarks referenced herein are registered trademarks of REGENXBIO.

CONTACTS: 

Dana Cormack
Corporate Communications
Dcormack@regenxbio.com

Chris Brinzey, ICR Westwicke
339-970-2843
Chris.Brinzey@westwicke.com

(PRNewsfoto/REGENXBIO Inc.)

 

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SOURCE REGENXBIO Inc.

FAQ

What is the pricing of the underwritten public offering announced by REGENXBIO Inc.?

REGENXBIO Inc. announced the pricing of an underwritten upsized public offering of 4,565,260 shares of its common stock at $23.00 per share and 1,521,740 pre-funded warrants at $22.9999 per warrant.

How much is REGENXBIO Inc. expecting to raise from the public offering?

REGENXBIO Inc. is expected to raise approximately $140.0 million from the public offering.

When is the expected closing date of the public offering by REGENXBIO Inc.?

The public offering by REGENXBIO Inc. is expected to close on March 11, 2024.

Which underwriters are acting as joint book-running managers of the offering for REGENXBIO Inc.?

Morgan Stanley, Goldman Sachs & Co. LLC, Barclays, and Stifel are acting as joint book-running managers of the offering for REGENXBIO Inc.

How many additional shares have the underwriters been granted the option to purchase?

The underwriters have been granted the option to purchase an additional 913,050 shares of common stock.

REGENXBIO Inc.

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About RGNX

regenxbio is a leading biotechnology company focused on the development, commercialization and licensing of recombinant adeno‐associated virus (aav) gene therapy. regenxbio's nav® technology platform, a proprietary aav gene delivery platform, consists of exclusive rights to more than 100 novel aav vectors, including aav7, aav8, aav9 and aavrh10. regenxbio's mission is to transform the lives of patients suffering from severe diseases with significant unmet medical need by developing and commercializing in vivo gene therapy products based on regenxbio's nav technology platform. regenxbio seeks to accomplish this mission through a combination of internal development efforts and third‐party nav technology platform licensees.