Phathom Pharmaceuticals Announces Placement of the Remaining $40 Million in Non-Dilutive Capital under its up to $300 Million Revenue Interest Financing Agreement
Phathom Pharmaceuticals (NASDAQ: PHAT) has secured an additional $40 million in non-dilutive financing, increasing total available financing to $300 million. This funding includes $15 million contingent upon FDA approval for vonoprazan in treating erosive esophagitis and $25 million linked to sales milestones. Investors will receive a 10% royalty on net sales, capped at 2.0x of total payments received. This agreement involves Sagard Healthcare Partners, NovaQuest Capital Management, and Hercules Capital.
- Secured an additional $40 million in non-dilutive financing, raising total financing to $300 million.
- Funding includes $15 million upon FDA approval of vonoprazan for erosive esophagitis.
- Potential $25 million milestone funding based on sales achievements.
- None.
- Up to
$40 million committed, resulting in total financing of up to$300 million available to Phathom with total royalty payments capped at 2.0x invested capital
- Provides agreement for additional
$15 million upon FDA approval of vonoprazan for treatment of erosive esophagitis (EE) and$25 million for achievement of a sales milestone
FLORHAM PARK, N.J., Nov. 01, 2022 (GLOBE NEWSWIRE) -- Phathom Pharmaceuticals, Inc. (Nasdaq: PHAT), a biopharmaceutical company focused on developing and commercializing novel treatments for gastrointestinal diseases and disorders, today announced that up to an additional
Up to
In exchange for the commitment to provide these cash payments, the investors will receive a
Morgan Stanley & Co. LLC acted as sole structuring agent on the transaction.
About Phathom Pharmaceuticals, Inc.
Phathom Pharmaceuticals is a biopharmaceutical company focused on the development and commercialization of novel treatments for gastrointestinal diseases and disorders. Phathom has in-licensed the exclusive rights in the United States, Europe, and Canada to vonoprazan, a first-in-class potassium-competitive acid blocker (PCAB). Vonoprazan-based regimens are approved in the U.S. as part of a co-packaged product in combination with antibiotics for the treatment of H. pylori infection in adults, marketed as VOQUEZNA™ TRIPLE PAK™ (vonoprazan, amoxicillin, clarithromycin) and VOQUEZNA™ DUAL PAK™ (vonoprazan, amoxicillin). Phathom has a New Drug Application under review by the FDA for vonoprazan in erosive esophagitis (EE) and is studying the use of vonoprazan for the treatment of non-erosive reflux disease (NERD). For more information about Phathom, visit the Company’s website at www.phathompharma.com and follow the Company on LinkedIn and Twitter.
CONTACTS
Media and Investor Contact:
Nick Benedetto
1-877-742-8466
media@phathompharma.com
ir@phathompharma.com
© 2022 Phathom Pharmaceuticals. All rights reserved.
VOQUEZNA, VOQUEZNA TRIPLE PAK, VOQUEZNA DUAL PAK, Phathom Pharmaceuticals, and their respective logos are registered trademarks or trademarks of Phathom Pharmaceuticals, Inc.
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