XOMA Royalty acquires seralutinib, enhancing its Phase 3 royalty assets targeting pulmonary arterial hypertension.
Quiver AI Summary
XOMA Royalty Corporation has acquired an economic interest in seralutinib, a Phase 3 asset being developed for pulmonary arterial hypertension (PAH), through its purchase of Pulmokine Inc. This marks XOMA Royalty's seventh Phase 3 royalty asset, enhancing its late-stage pipeline alongside six existing commercial assets. The Phase 3 study for seralutinib is ongoing, with results expected in the fourth quarter of 2025. The acquisition is positioned to yield up to $25 million in milestone payments and a low to mid-single digit royalty on future sales. This move reflects XOMA's strategy to grow its portfolio by offering innovative royalty capital solutions to biotechnology companies. The transaction underscores XOMA's commitment to advancing therapies that could benefit various cardio-respiratory conditions.
Potential Positives
- Seralutinib's inclusion as XOMA Royalty's seventh Phase 3 royalty asset strengthens the company's late-stage pipeline, enhancing its portfolio of commercial royalty assets.
- The potential to net up to $25 million in milestone payments represents a significant financial opportunity for XOMA Royalty, which could bolster its revenue stream.
- The ongoing Phase 3 study for pulmonary arterial hypertension (PAH) suggests a promising therapeutic advance, with expected results due in the fourth quarter of 2025.
- The acquisition of Pulmokine Inc. exemplifies XOMA Royalty's strategic approach to expanding its asset base and creating favorable outcomes for stakeholders, highlighting potential future value beyond PAH indications.
Potential Negatives
- The acquisition of Pulmokine for $20 million in cash indicates a significant financial commitment, and the success of this investment depends heavily on the outcomes of the ongoing Phase 3 study, which introduces uncertainty regarding potential returns.
- The company's royalties from seralutinib are expected to be low to mid-single digits, potentially limiting revenue generation and raising concerns about the overall scalability of its revenue model.
- The reliance on multiple development partners (Gossamer Bio and Chiesi Farmaceutici) for seralutinib's success could expose XOMA Royalty to risks associated with third-party performance and strategic decisions that may not align with XOMA's interests.
FAQ
What is seralutinib and its purpose?
Seralutinib is a drug in Phase 3 development targeting pulmonary arterial hypertension (PAH) and potentially other cardio-respiratory conditions.
Who are the partners involved in seralutinib's development?
Seralutinib is being co-commercialized by Gossamer Bio, Inc. and Chiesi Farmaceutici S.p.A.
What financial potential does XOMA Royalty see from seralutinib?
XOMA Royalty could earn up to $25 million in milestone payments and low to mid-single digit royalties from seralutinib sales.
What strategic benefit does XOMA gain from acquiring Pulmokine?
The acquisition adds seralutinib to XOMA's royalty portfolio, enhancing its late-stage pipeline and potential returns.
What other assets does XOMA Royalty currently hold?
XOMA holds a diverse portfolio that includes commercial assets like VABYSMO® and investigational compounds under development.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$XOMA Insider Trading Activity
$XOMA insiders have traded $XOMA stock on the open market 2 times in the past 6 months. Of those trades, 0 have been purchases and 2 have been sales.
Here’s a breakdown of recent trading of $XOMA stock by insiders over the last 6 months:
- THOMAS M. BURNS (SVP, Finance & CFO) sold 9,775 shares.
- OWEN HUGHES (Chief Executive Officer) sold 21,881 shares.
To track insider transactions, check out Quiver Quantitative's insider trading dashboard.
$XOMA Hedge Fund Activity
We have seen 30 institutional investors add shares of $XOMA stock to their portfolio, and 22 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- STONEPINE CAPITAL MANAGEMENT, LLC removed 55,033 shares (-22.0%) from their portfolio in Q3 2024
- FMR LLC removed 51,003 shares (-4.4%) from their portfolio in Q3 2024
- ACUITAS INVESTMENTS, LLC removed 35,139 shares (-28.5%) from their portfolio in Q3 2024
- BLACKROCK, INC. added 23,173 shares (+4.5%) to their portfolio in Q3 2024
- WOODLINE PARTNERS LP added 23,128 shares (+32.0%) to their portfolio in Q3 2024
- ELLSWORTH ADVISORS, LLC added 19,475 shares (+inf%) to their portfolio in Q3 2024
- MORGAN STANLEY added 15,736 shares (+9.4%) to their portfolio in Q3 2024
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
Full Release
S eralutinib becomes XOMA Royalty’s seventh Phase 3 royalty asset, further building the late-stage pipeline beyond its six current commercial royalty assets
Seralutinib is being developed and co-commercialized by Gossamer Bio, Inc., and Chiesi Farmaceutici S.p.A; a Phase 3 study for pulmonary arterial hypertension is ongoing and is expected to read out in the fourth quarter of 2025 1
XOMA Royalty has the potential to net up to $25 million in milestone payments and earn a low to mid-single digit royalty
EMERYVILLE, Calif., Dec. 02, 2024 (GLOBE NEWSWIRE) -- XOMA Royalty Corporation (NASDAQ: XOMA) announced today it now owns an economic interest in seralutinib, a Phase 3 asset being studied in pulmonary arterial hypertension (PAH), through its acquisition of Pulmokine Inc., a privately held company. In 2017, Pulmokine licensed seralutinib to Gossamer Bio, Inc., and in 2024, Gossamer Bio signed a global collaboration and license agreement with Chiesi Farmaceutici S.p.A.
“We acquired Pulmokine to add seralutinib, a Phase 3 asset with strong mechanistic rationale in PAH, to our growing royalty and milestone portfolio while creating a favorable outcome for Pulmokine’s founders and stockholders. In addition, we believe seralutinib has the potential to address several cardio-respiratory conditions beyond PAH in the future,” stated Brad Sitko, Chief Investment Officer of XOMA Royalty. “This transaction marks the second whole-company acquisition we have completed in 2024. We continue to offer creative royalty capital solutions to access assets with the potential to deliver attractive returns to XOMA Royalty’s diverse portfolio.”
Terms
XOMA Royalty acquired all outstanding shares of Pulmokine for a $20 million cash payment at closing. In addition, XOMA Royalty will pay success-based consideration contingent on future development and commercial events to Pulmokine stockholders. XOMA Royalty’s net royalties will range from the low to mid-single digits on commercial sales; additionally, the Company will retain up to $25 million of the milestone payments.
Advisors
XOMA Royalty was represented by Gibson, Dunn & Crutcher LLP.
About XOMA Royalty Corporation
XOMA Royalty is a biotechnology royalty aggregator playing a distinctive role in helping biotech companies achieve their goal of improving human health. XOMA Royalty acquires the potential future economics associated with pre-commercial therapeutic candidates that have been licensed to pharmaceutical or biotechnology companies. When XOMA Royalty acquires the future economics, the seller receives non-dilutive, non-recourse funding they can use to advance their internal drug candidate(s) or for general corporate purposes. The Company has an extensive and growing portfolio of assets (asset defined as the right to receive potential future economics associated with the advancement of an underlying therapeutic candidate). For more information about XOMA Royalty and its portfolio, please visit
www.xoma.com
or follow the Company on
LinkedIn
.
Forward-Looking Statements/Explanatory Notes
Certain statements contained in this press release are forward-looking statements, including statements regarding the potential indications for and therapeutic benefits of seralutinib and its potential to generate financial returns. In some cases, you can identify such forward-looking statements by terminology such as “anticipate,” “intend,” “believe,” “estimate,” “plan,” “seek,” “project,” “expect,” “may,” “will,” “would,” “could” or “should,” the negative of these terms or similar expressions. These forward-looking statements are not a guarantee of XOMA Royalty’s performance, and you should not place undue reliance on such statements. These statements are based on assumptions that may not prove accurate, and actual results could differ materially from those anticipated due to certain risks inherent in the biotechnology industry, including those related to the fact that our product candidates subject to out-license agreements are still being developed, and our licensees may require substantial funds to continue development which may not be available; we do not know whether there will be, or will continue to be, a viable market for the products in which we have an ownership or royalty interest; if the therapeutic product candidates to which we have a royalty interest do not receive regulatory approval, and our third-party licensees will not be able to market them. Other potential risks to XOMA Royalty meeting these expectations are described in more detail in XOMA Royalty's most recent filing on Form 10-Q and in other filings with the Securities and Exchange Commission. Consider such risks carefully when considering XOMA Royalty's prospects. Any forward-looking statement in this press release represents XOMA Royalty's beliefs and assumptions only as of the date of this press release and should not be relied upon as representing its views as of any subsequent date. XOMA Royalty disclaims any obligation to update any forward-looking statement, except as required by applicable law.
EXPLANATORY NOTE: Any references to “portfolio” in this press release refer strictly to milestone and/or royalty rights associated with a basket of drug products in development. Any references to “assets” in this press release refer strictly to milestone and/or royalty rights associated with individual drug products in development.
As of the date of this press release, the commercial assets in XOMA Royalty’s milestone and royalty portfolio are VABYSMO ® (faricimab-svoa), OJEMDA™ (tovorafenib), MIPLYFFA™ (arimoclomol), XACIATO™ (clindamycin phosphate) vaginal gel 2%, IXINITY ® [coagulation factor IX (recombinant)], and DSUVIA ® (sufentanil sublingual tablet). All other assets in the milestone and royalty portfolio are investigational compounds. Efficacy and safety have not been established. There is no guarantee that any of the investigational compounds will become commercially available.
| XOMA Royalty Investor Contact | XOMA Royalty Media Contact |
| Juliane Snowden | Kathy Vincent |
| XOMA Royalty Corporation | KV Consulting & Management |
| +1 646-438-9754 | +1 310-403-8951 |
| [email protected] | [email protected] |
1 https://ir.gossamerbio.com/news-releases/news-release-details/gossamer-bio-announces-third-quarter-2024-financial-results-and