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Agenus (AGEN) reported a dramatic turnaround in Q3 2025 earnings, with a net income of $63.91 million—representing a 195.1% positive swing from a $67.21 million loss in the prior year. The company also returned to profitability with an EPS of $2.00, reversing a $3.08 per share loss. Despite these gains,
did not provide explicit revenue or EPS guidance for future periods.Agenus’s total revenue surged 20.4% year-over-year to $30.23 million in Q3 2025. Research and development revenue stood at $1.09 million, while non-cash royalty revenue from the sale of future royalties accounted for $29.15 million. This segment breakdown highlights the company’s reliance on non-traditional revenue streams, particularly from its MiNK Therapeutics deconsolidation, which contributed a $100.9 million gain to Q3 net income.
Agenus returned to profitability with an EPS of $2.00 in Q3 2025, reversing a $3.08 per share loss in the prior year. The company achieved a remarkable 195.1% positive swing in net income, jumping to $63.91 million from a $67.21 million loss. This turnaround was driven by the MiNK deconsolidation gain and strategic financial moves, including a $10 million bridge facility with Zydus. The earnings performance underscores a significant shift in the company’s financial trajectory.
Agenus’s stock price surged 5.78% on the day of the earnings release and gained 6.05% over the subsequent trading week, reflecting strong investor optimism about the company’s turnaround. However, the stock edged down 0.94% month-to-date, indicating some short-term volatility. The post-earnings rally aligns with the company’s clinical and regulatory advancements, including France’s reimbursed access for its BOT/BAL therapy and the initiation of the global Phase 3 BATTMAN trial. Analysts suggest that the stock’s performance will hinge on the sustainability of these developments and future earnings momentum.
John D. Gray, President and CEO, emphasized clinical milestones in Q3 2025, including France’s reimbursed compassionate access for BOT/BAL in refractory MSS mCRC and the BATTMAN trial launch. He highlighted the combination’s potential to expand immunotherapy access to historically unresponsive cancers, citing 42% two-year survival rates in MSS mCRC. Financially, Gray noted the MiNK deconsolidation gain and the Zydus bridge facility as key enablers of the Q3 net income. The tone reflected confidence in both clinical progress and strategic financial positioning.
Agenus outlined key upcoming milestones, including the Q4 2025 launch of the BATTMAN Phase 3 trial and patient enrollment before year-end. The company anticipates investigator-initiated trials to provide neoadjuvant and frontline data updates in 1H 2026. France’s AAC program is expected to generate real-world evidence, while self-pay access in multiple regions remains active. The Zydus transaction, including a $7.50/share equity investment, is pending regulatory and financial terms. No explicit revenue or EPS guidance was provided.
Recent developments include Agenus’s MiNK Therapeutics deconsolidation, which generated a $100.9 million gain, and a $10 million bridge facility with Zydus ahead of a $91 million transaction. Additionally, the BATTMAN Phase 3 trial for BOT/BAL in MSS mCRC is set to launch in Q4 2025, supported by academic networks in Canada, France, Australia, and New Zealand. These moves underscore Agenus’s focus on expanding access to its therapies and strengthening its balance sheet through strategic partnerships and clinical advancements.

Agenus’s Q3 2025 results reflect a pivotal shift in its financial and operational performance, driven by clinical milestones and strategic deconsolidation gains. The company’s stock has seen a post-earnings rally, though future performance will depend on the success of its BATTMAN trial and broader market dynamics. Investors remain cautiously optimistic about Agenus’s long-term prospects.
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