Viking Therapeutics Announces Closing of Public Offering of Common Stock Including Full Exercise of Underwriters' Option to Purchase Additional Shares
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Insights
The successful closing of Viking Therapeutics' underwritten public offering is a significant financial milestone, indicating robust investor interest and a strong market appetite for the company's shares. The offering's size, with over 7 million shares at $85.00 each, resulting in gross proceeds of approximately $632.5 million, is substantial for a clinical-stage biopharmaceutical firm. This capital influx will bolster Viking's financial position, enabling accelerated development of its therapeutic programs. Furthermore, the full exercise of the underwriters' option to purchase additional shares underscores confidence in Viking's potential.
From a financial perspective, the involvement of prominent financial institutions as book-running managers and co-managers lends credibility to the offering. It is essential to note that the proceeds, before expenses, are considerable and are intended for the development of Viking's leading drug candidates and general corporate purposes. This allocation of funds is expected to catalyze the company's research and development efforts, potentially leading to advancements in treatments for metabolic and endocrine disorders.
Investors should monitor the efficiency and effectiveness of capital deployment as it can significantly impact Viking's future valuation and stock performance. The company's strategic focus on its VK2809, VK2735 and VK0214 programs will likely be a critical factor in its operational progress and success in the competitive biopharmaceutical landscape.
The capital raised by Viking Therapeutics through this public offering is poised to fund the continued development of its pipeline products, which target metabolic and endocrine disorders—a therapeutic area with significant unmet medical needs. The company's lead candidates, VK2809, VK2735 and VK0214, have the potential to address conditions such as non-alcoholic fatty liver disease, dyslipidemia and X-linked adrenoleukodystrophy, respectively.
It is crucial to understand the competitive landscape and the current stage of clinical development for these candidates. The success of these programs will be instrumental in determining Viking's market position and future revenue streams. Furthermore, the allocation of funds towards general research and development could lead to the discovery of new drug candidates, expanding Viking's portfolio and potential market reach.
Investors and stakeholders should consider the long-term implications of the company's R&D investments, as the biotech sector is characterized by high risk and high reward. The time frame for drug development and regulatory approval is lengthy and the outcome is uncertain, but successful product launches could significantly enhance shareholder value.
The offering was conducted under an automatic shelf registration statement on Form S-3, which allows for timely capital raising opportunities as market conditions become favorable. The immediate effectiveness of the shelf registration upon filing with the SEC simplifies the process of issuing new shares. However, it is imperative for the company to comply with the SEC's regulations and ensure that all the necessary disclosures are made to potential investors through the final prospectus supplement and accompanying prospectus.
Legal compliance in the biopharmaceutical industry is critical, not only in terms of financial offerings but also in the development and commercialization of drugs. Viking must navigate complex regulatory pathways to bring its drug candidates to market. The funds raised will likely be subject to scrutiny to ensure they are used as declared for development programs and corporate purposes and not for undisclosed activities that could lead to legal complications or investor mistrust.
Investors should be aware that any deviations from the stated use of proceeds or regulatory missteps in drug development could have legal and financial repercussions for the company, potentially affecting its stock price and investor confidence.
Morgan Stanley, Leerink Partners, William Blair, Raymond James, Stifel and Truist Securities acted as joint book-running managers for the offering. Oppenheimer & Co. acted as lead manager for the offering. BTIG, H.C. Wainwright & Co., Maxim Group LLC and Laidlaw & Company (
Viking currently intends to use the net proceeds from the offering for continued development of its VK2809, VK2735 and VK0214 programs and for general research and development, working capital and general corporate purposes.
The securities described above were offered by Viking pursuant to an automatic shelf registration statement on Form S-3 (File No. 333-273460), previously filed with the Securities and Exchange Commission (the "SEC") on July 26, 2023, and which automatically became effective upon filing. A final prospectus supplement and the accompanying prospectus relating to and describing the terms of the offering was filed with the SEC on March 1, 2024 and is available on the SEC's website at www.sec.gov. Copies of the final prospectus supplement and the accompanying prospectus relating to the offering may also be obtained by contacting Morgan Stanley & Co. LLC, Attention: Prospectus Department, 180 Varick Street, 2nd Floor,
This press release shall not constitute an offer to sell or the solicitation of an offer to buy, 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 the registration or qualification under the securities laws of any such state or jurisdiction.
About Viking Therapeutics, Inc.
Viking Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on the development of novel first-in-class or best-in-class therapies for the treatment of metabolic and endocrine disorders, with three compounds currently in clinical trials. Viking's research and development activities leverage its expertise in metabolism to develop innovative therapeutics designed to improve patients' lives. Viking's clinical programs include VK2809, a novel, orally available, small molecule selective thyroid hormone receptor beta agonist for the treatment of lipid and metabolic disorders, which is currently being evaluated in a Phase 2b study for the treatment of biopsy-confirmed non-alcoholic steatohepatitis (NASH) and fibrosis. In a Phase 2a trial for the treatment of non-alcoholic fatty liver disease (NAFLD) and elevated LDL-C, patients who received VK2809 demonstrated statistically significant reductions in LDL-C and liver fat content compared with patients who received placebo. Viking is also developing VK2735, a novel dual agonist of the glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) receptors for the potential treatment of various metabolic disorders. Data from a Phase 1 and a Phase 2a trial evaluating VK2735 (dosed subcutaneously) for metabolic disorders demonstrated an encouraging safety and tolerability profile as well as positive signs of clinical benefit. The company is also evaluating an oral formulation of VK2735 in a Phase 1 trial. In the rare disease space, Viking is developing VK0214, a novel, orally available, small molecule selective thyroid hormone receptor beta agonist for the potential treatment of X-linked adrenoleukodystrophy (X-ALD). VK0214 is currently being evaluated in a Phase 1b clinical trial in patients with the adrenomyeloneuropathy (AMN) form of X-ALD. Viking holds exclusive worldwide rights to a portfolio of five therapeutic programs, including VK2809 and VK0214, which are based on small molecules licensed from Ligand Pharmaceuticals Incorporated.
Forward-Looking Statements
This press release contains forward-looking statements under the safe harbor provisions of the
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SOURCE Viking Therapeutics, Inc.
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