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Pharma Mar (PHM) investor relations material
Pharma Mar Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Total revenues increased by 18% year-over-year to €95.3 million, with growth across all revenue streams, including recurring and nonrecurring income.
EBITDA reached €25.1 million, improving from negative €0.8 million, driven by strong licensing income and subsidies.
Net profit rose to €19.4 million, over five times higher than the prior year period.
Major regulatory milestones achieved for Zepzelca, including FDA priority review and EMA submission for SCLC.
R&D expenditure decreased to €47.5 million, with ongoing investment in oncology and RNAi clinical programs.
Financial highlights
Recurring revenue rose 5% to €72.2 million, with net sales up 9% to €45.8 million year-over-year.
Nonrecurring license revenues surged 87% to €23.0 million, mainly from a new Japanese license agreement.
Upfront payment of €22 million from a Japanese license agreement, with €21.7 million recognized as revenue by June 30.
Operating profit reached €21.1 million, compared to a loss of €3.9 million in 1H24.
Cash and equivalents plus financial investments totaled €182.9 million at period end.
Outlook and guidance
EMA review for first-line maintenance treatment in SCLC underway, with opinion expected by Q1 2026 and product launch preparations ongoing.
FDA PDUFA date for a key product set for October 7, with additional regulatory reviews in Israel, Switzerland, Australia, and Singapore expected soon after.
R&D spending expected to intensify in coming quarters due to new early-stage clinical developments.
SCLC trial results (LAGOON) anticipated in 1H26, with potential for expanded indications.
Anticipated inclusion of new combination therapy in NCCN guidelines following positive trial results.
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