Eisai Co (4523N) Q1 2026 Earnings Report
MX:4523N Q1 2026 EPS Results
- Actual EPS
- MXN 7.70
- Consensus EPS
- MXN 6.60
- Beat/Miss
- Beat by +MXN 1.11
- One Year Ago EPS
- MXN 6.11
MX:4523N Q1 2026 Revenue Results
- Actual Revenue
- MXN 27.88B
- Expected Revenue
- MXN 25.59B
- Beat/Miss
- Beat by +MXN 2.30B
- YoY Revenue Growth
- +15.63%
Earnings Announcement Details
- Quarter
- Q1 2026
- Date
- 08/03/2026
- Time
- Before Open
- Conference Call
- Monday, August 3, 2026
Eisai Co's next earnings date is estimated for November 10, 2026, based on past reporting schedules.
Q1 2026 Earnings Call Audio
Q1 2026 Earnings Slide Deck
Q1 2026 Earnings Call Summary
The call conveys clear commercial momentum and strong financial improvement driven by the flagship products (notably LEQEMBI and LENVIMA), meaningful cost-efficiency gains, and reinforcing clinical and real-world evidence. Key near-term catalysts include SC‑AI approval, BBM reimbursement and ongoing DTC/pathway initiatives. Material risks discussed include pricing and HTA uncertainty in Japan, potential tariff/MFN policy impacts, reimbursement execution (Medicare Part B to D transition) and competitive entrants. On balance the positives — robust revenue and profit growth, expanding diagnostics and pathway adoption, favorable clinical data and operating leverage — outweigh the uncertainties, though continued monitoring of pricing/reimbursement and geopolitical policy is warranted.
Management reiterated there is no change to the consolidated FY2025 forecast and said Q1 was a strong start: consolidated revenue JPY202.7bn (+7% YoY; FX headwind JPY10.1bn), pharmaceutical revenue JPY198.4bn (+6%), gross profit JPY160.1bn (+7%) with cost of sales JPY42.6bn (cost ratio 21%), R&D JPY38.8bn (93% of prior year; 19.1% of revenue, down ~3ppt from 22.1%), SG&A JPY100.2bn (+1%, including JPY36.0bn shared profit), operating profit JPY20.7bn (+55%), net profit JPY15.3bn (+33%) and profit attributable to owners JPY14.5bn (+37%); 3Ls (LENVIMA, LEQEMBI, DAYVIGO) totaled JPY120.7bn (+19% YoY) with LEQEMBI driving a JPY16.9bn uplift. Product guidance reiterated: LEQEMBI Q1 sales JPY23.1bn and FY2025 sales target JPY76.5bn, LENVIMA Q1 JPY83.9bn and FY2025 target JPY312bn; company targets FY2026 ROE 8% and revenue JPY790bn/operating profit JPY54.5bn. Key operational catalysts and timing noted include the SC‑AI PDUFA action date Aug 31 (360 mg weekly SC‑AI shown equivalent to 10 mg/kg monthly IV), BBM diagnostic guidance (triage tests ≥90% sensitivity/≥75% specificity; substitute tests ≥90%/≥90%) and expected BBM reimbursement/pricing from January, plus demand indicators such as US LEQEMBI +20% QoQ (CER), BBM tests +130% average growth, PET/CSF tests +120% average growth, Japan wholesaler shipments 130% QoQ and 1,500 follow‑up facilities established.
- Revenue and Profit GrowthConsolidated revenue increased 7% YoY to JPY 202.7 billion (Q1 FY2025). Operating profit rose 55% YoY to JPY 20.7 billion; net profit increased 33% YoY to JPY 15.3 billion; profit attributable to owners up 37% YoY to JPY 14.5 billion.
- Pharmaceutical Segment and 3Ls ExpansionPharmaceutical revenue JPY 198.4 billion (+6% YoY). Revenue from the 3Ls (LENVIMA, LEQEMBI, DAYVIGO) was JPY 120.7 billion, up 19% YoY, with LEQEMBI accounting for the largest incremental increase (+JPY 16.9 billion YoY).
- LEQEMBI Commercial MomentumGlobal LEQEMBI Q1 revenue JPY 23.1 billion with double-digit growth in Japan, the U.S., China and other regions; company states progress is on track toward FY2025 sales forecast of JPY 76.5 billion.
- U.S. Demand Expansion & Diagnostic AdoptionU.S. LEQEMBI sales grew ~20% QoQ on a constant exchange rate basis. Blood biomarker (BBM) triage tests increased on average >130% and PET/CSF confirmatory tests increased >120%, supporting pathway expansion and earlier diagnosis.
- SC‑AI Maintenance Therapy ProgressPDUFA date for SC-AI maintenance therapy set for Aug 31, with modeling and human-factor data indicating PK/PD equivalence to IV maintenance; SC-AI enables weekly, home administration (avg ~15 seconds) and is expected to expand access and reduce health-system costs.
- Clinical and Real‑World Evidence Strengthening ValueAAIC presentations included 48-month continued-treatment data showing sustained benefits vs natural history and 2-year real-world data where ~84% of patients did not progress; high stakeholder satisfaction (patients 8.8/10, physicians 8.7/10).
- Cost Efficiency and Margin ImprovementsR&D expenses decreased to JPY 38.8 billion (93% of prior year) and R&D ratio fell to 19.1% of revenue (down ~3 points). SG&A rose 1% to JPY 100.2 billion but SG&A ratio decreased ~3.2 points, contributing to gross and operating profit expansion.
- LENVIMA Steady Performance and IP WinQ1 global LENVIMA revenue JPY 83.9 billion with steady progress (104% vs prior year on CER wording in call). Maintains top market shares in renal cell and endometrial carcinoma and key TKIs; favorable high‑purity patent lawsuit decision supports value maximization.
MX:4523N Earnings History
| Report Date | Fiscal Quarter | Forecast / EPS | Last Year's EPS | EPS YoY Change | Press Release |
|---|---|---|---|---|---|
| Nov 10, 2026 | 2026 (Q2) | 6.92- | 4.29 | ― | ― |
| Aug 03, 2026 | 2026 (Q1) | 6.607.70 | 6.11 | 26.02% (+1.59) | |
| May 15, 2026 | 2025 (Q4) | 1.48-1.37 | 0.43 | -418.51% (-1.80) | |
| Feb 09, 2026 | 2025 (Q3) | 8.757.25 | 10 | -27.46% (-2.75) | |
| Nov 05, 2025 | 2025 (Q2) | 5.814.29 | 4.66 | -8.07% (-0.38) | |
| Aug 05, 2025 | 2025 (Q1) | 4.616.11 | 4.4 | 38.97% (+1.71) | |
| May 15, 2025 | 2024 (Q4) | 2.190.43 | 5.52 | -92.20% (-5.09) | |
| Feb 07, 2025 | 2024 (Q3) | 5.0810.00 | 2.48 | 303.51% (+7.52) | |
| Nov 08, 2024 | 2024 (Q2) | 3.654.66 | 1.16 | 303.09% (+3.51) | |
| Aug 02, 2024 | 2024 (Q1) | 3.304.40 | 8.44 | -47.90% (-4.04) |
The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.
