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Ligand Pharmaceuticals (NASDAQ: LGND) delivered a mixed yet compelling performance in its first quarter of 2025, showcasing robust revenue growth driven by its royalty-driven model while facing a one-time charge that dented its reported earnings. The results underscore the company’s ability to navigate industry challenges through strategic partnerships and diversified assets, even as it grapples with short-term headwinds.
Ligand’s Q1 2025 revenue surged 46% year-over-year to $45.3 million, fueled by a 44% jump in portfolio royalty revenue to $27.5 million and a 47% rise in Captisol® sales to $13.5 million. This outperformance reflects strong commercial traction from key partner products, such as Verona Pharma’s Ohtuvayre and Merck’s Capvaxive. However, GAAP net loss widened to $42.5 million, or $2.21 per share, versus net income of $86.1 million in Q1 2024. The disparity stems from a one-time $44.3 million R&D charge tied to a royalty financing agreement with Castle Creek Biosciences for its DEB treatment, D-Fi.
When excluding this non-cash item and other adjustments, core adjusted net income rose 22% to $26.6 million, or $1.33 per share, exceeding the prior year’s $1.20. This metric better reflects Ligand’s operational performance, as its business model relies heavily on non-GAAP metrics due to contingent liabilities and equity method investments.

Ligand reinforced its growth trajectory through two transformative deals. First, it announced a merger with Channel Therapeutics, combining its Pelthos subsidiary to create a focused commercial entity. The merged company, Pelthos Therapeutics Inc., will receive a $50 million investment led by outside investors, with Ligand contributing $18 million. The new entity will commercialize ZELSUVMI, the first FDA-approved treatment for molluscum contagiosum, a niche indication with limited alternatives.
Second, Ligand advanced its stake in Castle Creek’s D-Fi program with a $75 million investment, including a $50 million equity infusion and a mid-single-digit royalty on future sales. This aligns with Ligand’s strategy of funding late-stage programs to secure long-term revenue streams.
Ligand’s partners are delivering on expectations, bolstering its royalty pipeline:
- Verona Pharma’s Ohtuvayre achieved $71.3 million in Q1 sales, a 95% quarterly jump, as the inhaled therapy gains traction for chronic obstructive pulmonary disease (COPD).
- Travere Therapeutics’ Filspari secured European Commission approval for pulmonary arterial hypertension, expanding its commercial footprint.
- Merck’s Capvaxive, a next-gen pneumococcal vaccine, saw Q1 sales surge 120% to $107 million, reflecting strong demand in pediatric markets.
- Palvella Therapeutics’ Qtorin advanced to Phase 2/3 trials, now including younger patients, enhancing its potential market reach for microcystic lymphatic malformations.
These milestones validate Ligand’s “royalty aggregation” model, which reduces reliance on internal drug development and instead leverages partner successes to generate steady cash flows.
Ligand reaffirmed its 2025 guidance of $180–$200 million in total revenue and adjusted EPS of $6.00–$6.25, reflecting confidence in its portfolio. With $208.9 million in cash as of March 31, the company maintains ample liquidity to fund strategic initiatives amid a challenging biopharma financing environment.
Risks persist, however. Ligand’s performance hinges on partner execution, regulatory approvals, and market competition. For instance, D-Fi’s commercial success depends on Castle Creek’s ability to navigate DEB’s complex patient landscape. Still, the diversified portfolio—spanning 15 marketed products and 30+ late-stage assets—mitigates single-drug dependency, a critical advantage in volatile markets.
Ligand’s Q1 results highlight a company capitalizing on its strengths while managing transient costs. The 46% revenue growth, $26.6 million adjusted net income, and $200+ million cash balance position it to capitalize on its strategic bets. The merger with Channel and investment in D-Fi aim to convert pipeline assets into recurring revenue streams, a hallmark of its repeatable model.
Investors should focus on adjusted metrics and the diversified partner portfolio, which have historically insulated Ligand from industry headwinds. While the one-time charge and GAAP loss may deter short-term traders, the fundamentals—strong cash flow, robust partner performance, and disciplined capital allocation—suggest Ligand remains a high-conviction play in the royalty-driven biotech space.
With its $27.5 million quarterly royalty revenue growing at 44% year-over-year and $107 million in Capvaxive sales alone, the path to achieving its $200 million revenue guidance is clear. For long-term investors, Ligand’s ability to turn strategic bets into sustained growth positions it well to outperform peers in the coming years.
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