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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
MX:4523N Upcoming Earnings

Eisai Co's next earnings date is estimated for November 10, 2026, based on past reporting schedules.

Q1 2026 Earnings Call Audio

MX:4523N Q1 2026 Earnings Call
0:00 / 0:00

Q1 2026 Earnings Slide Deck

Q1 2026 Earnings Call Summary

Q1 2026
Earnings Call Date:Aug 03, 2026|% Change Since:―|
Earnings Call Sentiment|Positive

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.

Company Guidance

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

MX:4523N earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Nov 10, 20262026 (Q2)6.92-4.29――
Aug 03, 20262026 (Q1)6.607.706.1126.02% (+1.59)
May 15, 20262025 (Q4)1.48-1.370.43-418.51% (-1.80)
Feb 09, 20262025 (Q3)8.757.2510-27.46% (-2.75)
Nov 05, 20252025 (Q2)5.814.294.66-8.07% (-0.38)
Aug 05, 20252025 (Q1)4.616.114.438.97% (+1.71)
May 15, 20252024 (Q4)2.190.435.52-92.20% (-5.09)
Feb 07, 20252024 (Q3)5.0810.002.48303.51% (+7.52)
Nov 08, 20242024 (Q2)3.654.661.16303.09% (+3.51)
Aug 02, 20242024 (Q1)3.304.408.44-47.90% (-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.

Beat Missed
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