Filed by Xeris Pharmaceuticals, Inc.
pursuant to Rule 425 under the Securities Act of 1933
and deemed filed pursuant to Rule 14a-12
under the Securities Exchange Act of 1934
Subject Company: Strongbridge Biopharma plc
Commission File No.: 001-37569
Date: August 6, 2021
The following communication is being filed in connection with the proposed acquisition of Strongbridge Biopharma plc by Xeris Pharmaceuticals, Inc.
Excerpts from the transcript of Xeris Pharmaceuticals, Inc.’s second quarter financial results and corporate update conference call held on Thursday, August 5, 2021.
Allison Wey Good morning and welcome to Xeris Pharmaceuticals’ second quarter 2021 financial results and corporate update conference call. A press release with the company’s second quarter financial results was issued earlier this morning and can be found on our website.
We are joined this morning by Paul Edick, Chairman and CEO, and Steve Pieper, our new CFO. Paul will provide opening remarks, Steve will provide details of our financial results, and then we will open lines for Q&A. John Johnson and Rich Kollender from Strongbridge will also be available to answer select questions. We would like to remind you that the Strongbridge transaction is subject to the Irish takeover rule, and as a result we may be restricted from answering certain questions.
Before we begin, I would like to remind you that this call will contain forward-looking statements concerning the impact of COVID-19 on Xeris’s business practice, Xeris’s future expectations, plans, prospects, clinical approval, commercialisation, corporate strategy, and performance, which constitute forward-looking statements for the purposes of the safe harbour provision under the Private Securities Litigation Reform Act of 1995.
Actual results may differ materially from those indicated by the forward-looking statements as a result of various important factors, including the effect of uncertainties related to the COVID-19 pandemic global market, Xeris’s business, financial condition, operation, clinical trial, and third-party suppliers and manufacturers, and other risks, including those discussed in our filing with the SEC.
In addition, any forward-looking statements represent our view only as the date of this call and should not be relied upon as representing our view as of any subsequent date. We specifically disclaim any obligations to update such statements. Like to turn the call over to Paul.
Paul Edick Thanks, Allison. Good morning to everyone who’s listening. We appreciate your interest in Xeris and in our discussion this morning…
Equally important was the announcement of the proposed acquisition of Strongbridge Biopharma, a major step to becoming a more commercially focused rare disease and speciality pharma company, which we’ll discuss in more detail as well in my follow-on remarks.
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…With our intensified focus on the commercial business, especially with the anticipated close of the Strongbridge Biopharma acquisition, we’re reprioritizing our approach to our pipeline and will focus our development efforts going forward solely on products for our own potential commercialisation…
Now I’d like to spend some time discussing the Strongbridge Biopharma acquisition and revisiting why this is the perfect combination in our minds for Xeris. First, by bringing Xeris and Strongbridge together, we’re creating a scalable and diversified biopharmaceutical company increasingly oriented toward more speciality and rare disease products.
We will have a strong revenue base with two rapidly growing assets, Gvoke and Keveyis. We will also have the opportunity for a near-term launch of Recorlev, and subject to FDA approval, we will be well positioned to leverage Xeris’s experience, endocrinology-focused commercial infrastructure to bring Recorlev to market. Our commercial footprint in endocrinology is larger than Strongbridge had envisioned for the launch of Recorlev, enabling a greater potential reach at launch.
We will also have an overall more robust rare disease and endocrinology-focused commercial infrastructure into which we can add additional products benefiting a broader range of patients. We also expect that new products will be brought forward in these therapeutic areas using our unique formulation technology platforms to put into a larger and scalable infrastructure for continued development of speciality-oriented and rare disease products from XeriSol and XeriJect.