XR
XOMA Royalty Corp (XOMA)·Q1 2025 Earnings Summary
Executive Summary
- XOMA delivered a materially stronger quarter: total income and revenues rose to $15.9M vs $1.5M a year ago, driving net income of $2.4M and diluted EPS of $0.06, aided by VABYSMO EIR income, Day One/Ipsen MAA milestone ($4.0M), Takeda collaboration payment ($4.0M), and OJEMDA royalties ($1.5M) .
- Consensus was far too low: Q1 revenue/“total income and revenues” of $15.9M vs $7.1M consensus*; EPS $0.06 vs -$0.27 consensus*, a significant beat that should reset near-term expectations higher.
- Cash receipts accelerated to $18.0M in Q1 (royalties/commercial payments $13.4M; milestones/fees $4.6M); quarter-end cash and equivalents were $95.0M (incl. $4.8M restricted) after $5.0M deployed on a new Phase 3 asset, $0.5M in buybacks, and $1.4M preferred dividends .
- Pipeline/catalysts: EMA review of tovorafenib (OJEMDA) underway; Takeda dosed first patient in mezagitamab Phase 3 (triggering a $3.0M milestone in Q2); multiple 2025 readouts/steps (e.g., Rezolute RZ358 topline Dec-2025; Gossamer seralutinib Phase 3 data) support continued royalty momentum .
Values marked with an asterisk are retrieved from S&P Global.
What Went Well and What Went Wrong
- What Went Well
- Strong top-line drivers: $15.9M total income and revenues (vs $1.5M prior year), led by VABYSMO EIR income, $4.0M Day One/Ipsen MAA milestone, $4.0M Takeda collaboration payment, and $1.5M OJEMDA royalties .
- Cash flow momentum: $18.0M cash receipts in Q1 (royalties/commercial $13.4M; milestones/fees $4.6M) and share repurchase of 25,828 shares for ~$0.5M reflecting capital discipline .
- Positive tone on sustainability: “With accelerating royalty receipts and a robust pipeline, we believe a path to sustained cashflow generation is tangible,” CEO Owen Hughes .
- What Went Wrong
- Other income headwind: Other income/expense swung to a small net expense (-$0.1M) vs +$2.0M prior year, due to lower equity values and lower investment income as balances and market rates declined .
- Ongoing interest burden: Q1 interest expense remained high at $3.5M tied to the Blue Owl loan (vs $3.6M in Q1’24) .
- R&D uptick (transitory): R&D rose to $1.3M vs $33K prior year, primarily pass-through licensing fees related to Takeda’s Phase 3 milestone and KIN-3248 clinical wind-down costs .
Financial Results
Summary financials vs prior periods
Notes: Company reports “Total income and revenues,” which includes income from purchased receivables and contract revenue.
Q1 2025 vs Wall Street consensus (S&P Global)
Values marked with an asterisk are retrieved from S&P Global.
Expenses and cash metrics (trend)
Guidance Changes
Earnings Call Themes & Trends
Note: We did not find a Q1 2025 earnings call transcript; themes reflect management’s press release commentary and prior quarter communications.
Management Commentary
- CEO Owen Hughes: “With accelerating royalty receipts and a robust pipeline, we believe a path to sustained cashflow generation is tangible.”
- CFO Tom Burns: “We received $18 million in cash, $13.4 million from our partners’ commercial sales and $4.6 million from milestones and fees…we deployed $0.5 million to repurchase 25,828 shares of our common stock.”
Q&A Highlights
- No Q1 2025 earnings call transcript was available; no Q&A themes to report from a call. All commentary sourced from the press release and 8‑K filing .
Estimates Context
- XOMA materially beat Q1 consensus: revenue/“total income and revenues” $15.9M vs $7.1M consensus* and EPS $0.06 vs -$0.27 consensus*, driven by EIR income on VABYSMO, Day One/Ipsen MAA milestone, Takeda collaboration payment, and OJEMDA royalties .
- Given the magnitude and composition of the beat, estimates likely need to incorporate continuing EIR contributions and upcoming milestone cadence (e.g., $3.0M net milestone from Takeda triggered in Q2) .
Values marked with an asterisk are retrieved from S&P Global.
Key Takeaways for Investors
- Q1 upside was driven by diversified cash flows: EIR income (VABYSMO), regulatory milestones (Day One/Ipsen), collaboration payments (Takeda), and initial OJEMDA royalties—supporting the royalty-aggregator model’s resilience .
- Cash receipts accelerated to $18.0M, and management reiterated a tangible path to sustained cash flow generation; this should be supportive for sentiment and near-term estimate revisions .
- Interest expense (~$3.5M/quarter) remains a drag tied to the Blue Owl loan; monitoring deleveraging or refinancing options is prudent .
- Expense normalization into 2H25 should aid operating leverage as acquisition-related costs subside, though quarterly noise (e.g., pass-through fees) can persist .
- Catalysts: EMA decision on tovorafenib; RZ358 Phase 3 topline (Dec-2025); Gossamer seralutinib Phase 3 readout; and Takeda’s mezagitamab Phase 3 progress—each could add to royalty momentum .
- Capital allocation remains balanced: continued portfolio build (Castle Creek D‑Fi), modest buybacks ($0.5M), and steady preferred dividends; cash of $95.0M provides flexibility .
- Near-term trading setup: substantial beat vs consensus and accelerating receipts provide a positive narrative; watch upcoming milestones/regulatory events for incremental inflections.
Sources
- Q1 2025 earnings 8‑K and press release (Ex. 99.1): totals, expenses, cash, milestones, quotes ; press release mirror .
- Prior quarters: Q4 2024 press release and 8‑K (trend, expenses, credit losses, cash) . Q3 2024 press release and 8‑K (trend, expenses, impairment) .
Values marked with an asterisk are retrieved from S&P Global.