Revenue Growth and Profitability
Total revenues of $3.5 billion, up 3% year-over-year (operational basis); adjusted EBITDA of $1.0 billion (10% growth year-over-year) and adjusted EPS of $0.59, demonstrating improved earnings leverage versus revenue growth.
Strong Greater China Performance
Greater China revenue accelerated 18% year-over-year, driven by favorable market fundamentals, strategic commercial investments and e-commerce growth (e-commerce sales more than doubled vs. prior year). Company raised its China growth expectation for 2026 to mid- to high-single digits.
Robust Pipeline Progress and Near-Term Catalysts
Regulatory approval received for EFFEXOR for GAD in Japan; NDA for fast-acting meloxicam accepted by FDA and XULANE LO (low-dose estrogen patch) expected PDUFA July 30, 2026; phentolamine sNDA PDUFA Oct 17, 2026. Company remains on track for 5 additional regulatory decisions in H2 2026 and multiple launches expected to accelerate growth.
Clinical Program Momentum in Late-Stage Programs
Selatogrel SOS-AMI Phase III enrollment ~1,200 patients per month and on track potentially to reach full enrollment by end of 2026; cenerimod Phase III SLE OPUS-1 and 2 fully enrolled with results expected in H1 2027 — representing material longer-term growth opportunities.
New Product Revenue Contribution and Complex Generics
New product revenue contribution of $71 million in the quarter (including launches of iron sucrose and octreotide); secured approval of a generic to Abilify Maintena and positioned for U.S. launch before year-end; on-track for FDA decisions this year on other complex generics (e.g., ferric carboxymaltose injection, rotigotine patch).
Margin and Cost Management
Adjusted gross margin of 56% (flat year-over-year) with margins slightly better than expected due to favorable product mix; operating expenses favorable versus prior year reflecting disciplined cost management and early realization of enterprise-wide strategic review savings (on track to deliver planned savings).
Strong Cash Generation and Capital Flexibility
Generated $348 million of cash in the quarter (or ~$459 million excluding transaction/restructuring costs and taxes); returned $140 million to shareholders via dividend; expecting more than $2.5 billion of cash available for deployment during 2026 to support dividends, buybacks, BD and reinvestment.
Clinical and Regulatory Evidence Supporting Label Expectations
Company believes data support inclusion of opioid-sparing language for fast-acting meloxicam label and presented positive Phase III and other data across programs (e.g., XULANE LO adhesion and PK data presented at ACOG).
Product-Specific Data and Development Wins
Creon Phase III interim analysis in non-cystic fibrosis patients showed ~76% of patients inadequately treated on current approved dose benefitted from dose escalation; plans to file a type 2 variation in Europe before year-end to drive future growth and label update in H1 2027.
Reaffirmed Guidance and Second-Half Weighting
Management reaffirmed 2026 guidance ranges and expects total revenues, adjusted EBITDA and adjusted EPS to be weighted to the second half (~52% of full-year outlook) reflecting seasonality and timing of launches.