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BioNTech SE (BNTX) Q3 2026 Earnings Report

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BNTX Q3 2026 EPS Results

Actual EPS
$0.81
Consensus EPS
$0.74
Beat/Miss
Beat by +$0.07
One Year Ago EPS
-$0.13

BNTX Q3 2026 Revenue Results

Actual Revenue
$1.48B
Expected Revenue
$1.15B
Beat/Miss
Beat by +$337.36M
YoY Revenue Growth
-16.44%

Earnings Announcement Details

Quarter
Q3 2026
Date
11/03/2026
Time
Before Open
Conference Call
Tuesday, November 3, 2026
BNTX Upcoming Earnings

BioNTech SE's next earnings date is estimated for March 2, 2027, based on past reporting schedules.

Q3 2026 Earnings Call Audio

BNTX Q3 2026 Earnings Call
0:00 / 0:00

Q3 2026 Earnings Slide Deck

Q3 2026 Earnings Call Summary

Q3 2026
Earnings Call Date:Nov 03, 2026|% Change Since:-2.20%|
Earnings Call Sentiment|Positive

The call was broadly optimistic, supported by strong gotistobart survival data, encouraging pumitamig combination results, a growing late-stage pipeline, a substantial cash balance, and a raised revenue-guidance midpoint. However, the company also reported lower COVID-19-related revenue, higher R&D and SG&A expenses, discontinuation of the colorectal cancer trial, a missed progression-free survival endpoint for BNT113, and limitations and safety concerns around T-Pam. The highlights significantly outweighed the lowlights, although several clinical programs remain subject to upcoming readouts and development decisions.

Company Guidance

BioNTech raised its full year 2026 revenue guidance to EUR 1.7 billion to EUR 1.9 billion, while maintaining adjusted R&D expense guidance of EUR 2 billion to EUR 2.3 billion and adjusted SG&A expense guidance of EUR 700 million to EUR 800 million; it expects the first interim analysis for gotistobart in squamous non-small cell lung cancer before year-end, a second one next year, first trials for pumitamig and Alpha-D novel combinations to begin in 2027, first-line TNBC in China data in 2027, ROSETTA Lung-02 and ROSETTA Lung-01 around 2029, and readouts for RCC, CRC, HCC, and the other studies thereafter, while it has seven global pivotal studies ongoing by end of this year and remains on track to become a diversified multi-product company by 2030.

  • Gotistobart Nearly Doubled Median Overall SurvivalIn the non-pivotal stage of the global phase III trial in metastatic squamous non-small cell lung cancer after prior checkpoint inhibitor treatment, gotistobart produced median overall survival of 18.5 months versus 10 months with docetaxel, with a hazard ratio of 0.56 and a 44% reduction in the risk of death compared with chemotherapy. The pivotal stage is ongoing, with an interim analysis anticipated before year-end.
  • Strong Pumitamig and Alpha-D Combination Data in Small Cell Lung CancerIn 71 small cell lung cancer patients across four dose levels, pumitamig plus Alpha-D produced a 92% overall response rate in first-line treatment, a 76% objective response rate in second-line treatment, and a 52% objective response rate in third-line and later treatment. Objective response rates were 60% in patients previously treated with immunotherapy and 88% in the small group previously treated with a DLL3-targeted T-cell engager.
  • Manageable Safety Profile for Pumitamig Plus Alpha-DThe pumitamig and Alpha-D combination had a manageable safety profile consistent with the individual agents, with limited overlap between toxicities, no dose-limiting toxicities, and an interstitial lung disease rate of 2.9%. The data support further development of pumitamig as a combination backbone, with first potential registration trials expected to begin in 2027.
  • Expansion of Pumitamig Combination StrategyBioNTech entered a clinical trial collaboration and supply agreement with Gilead to evaluate pumitamig with a TROP2-directed ADC as first-line treatment for metastatic PD-L1-low or negative triple-negative breast cancer. Pending regulatory approval, the study would be the first global phase III trial of pumitamig in combination with an ADC. BioNTech also has signal-seeking combination trials ongoing across its ADC portfolio, including its own TROP2 ADC, BMS assets, and partner assets.
  • Encouraging Triple-Negative Breast Cancer ResultsIn first-line metastatic triple-negative breast cancer, pumitamig combined with a TROP2-targeted ADC generated a confirmed objective response rate of 76.7% and a disease control rate of 96.7% in 30 patients. BioNTech is adapting ROSETTA Breast-01 to replace chemotherapy with sacituzumab govitecan to reflect the evolving treatment landscape.
  • Broad Late-Stage Oncology PipelineBioNTech reported seven global pivotal studies ongoing by the end of 2026 and said it initiated six phase III trials during 2026. The late-stage pipeline spans multiple tumor types and treatment lines, including lung, breast, renal cell carcinoma, colorectal, hepatocellular, gastrointestinal, and genitourinary cancers, with the company targeting a diversified multi-product business by 2030.
  • T-Pam Trial Met Its Primary EndpointThe global phase III trial of T-Pam, an investigational HER2 ADC in collaboration with DualityBio, met its primary endpoint in chemotherapy-naive patients with HR-positive, HER2-low metastatic breast cancer after endocrine therapy, showing a statistically significant improvement in progression-free survival. Overall-survival data were not mature at the interim analysis.
  • Financial Position and Revenue Guidance ImprovementBioNTech ended the third quarter with EUR 16.2 billion in cash equivalents and security investments. Following third-quarter performance, the company raised the midpoint of its full-year 2026 revenue guidance to EUR 1.7 billion to EUR 1.9 billion from the previously provided range.
  • Strategic Partnership Revenue ContributionThird-quarter revenue included EUR 613 million recognized from the global strategic partnership with BMS related to the co-development and co-commercialization of pumitamig.
  • Cost Discipline and Capital AllocationDespite increased investment in prioritized IO and ADC programs, BioNTech said it continues to realize meaningful savings from strategic pipeline prioritization and enhanced cost discipline. The company is prioritizing late-stage programs, selectively investing in earlier-stage innovation, consolidating its manufacturing footprint, and assessing additional areas to improve operational efficiency.
  • Share Repurchases and Balance-Sheet FlexibilitySince implementing its share buyback program in June, BioNTech had repurchased approximately 5 million shares through September 30. Management said the balance sheet provides flexibility to advance the pipeline, execute partnerships, pursue corporate development opportunities, and continue returning capital to shareholders.
  • mRNA Remains a Strategic PillarManagement reiterated that mRNA remains a key pillar of the oncology strategy. BioNTech continues to advance BNT113, BNT116, the pancreatic cancer program with Genentech, FixVac, the off-the-shelf platform, individualized vaccines, and other early-stage mRNA efforts. The ongoing phase II pancreatic cancer trial continues as planned.
  • Improved Financial Structure for the Genentech CollaborationBioNTech exercised a contractual option under its Roche/Genentech collaboration to transition future R&D costs for the program, including the pancreatic cancer indication, to Roche/Genentech. Beginning January 1, the economics will transition from 50/50 cost-profit sharing to royalty-based economics, while BioNTech remains eligible for royalties and the ongoing pancreatic cancer trial continues.
  • Integration of InstaDeep's AI CapabilitiesBioNTech plans to integrate the expertise and capabilities of InstaDeep, its wholly owned AI and machine-learning subsidiary, into the core business. The company said the initiative will focus AI development on strategic objectives, operational processes, and innovation priorities and is intended to reduce complexity.
  • Leadership Transition PlanningGuido Oelkers is expected to become CEO by February 1 at the latest. Management and the supervisory board said they have been actively engaged in supporting a seamless transition, while Uğur Şahin and Özlem Türeci will continue to follow BioNTech as founding shareholders.

BNTX Earnings History

BNTX earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Mar 02, 20272026 (Q4)-1.89--1.39――
Nov 03, 20262026 (Q3)0.740.81-0.13708.33% (+0.94)
Aug 04, 20262026 (Q2)-2.33-3.60-1.78-102.50% (-1.82)
May 05, 20262026 (Q1)-2.44-2.33-1.92-21.39% (-0.41)
Mar 10, 20262025 (Q4)-0.18-1.391.2-215.74% (-2.59)
Nov 03, 20252025 (Q3)-1.06-0.130.9-114.81% (-1.03)
Aug 04, 20252025 (Q2)-2.53-1.78-3.7352.38% (+1.95)
May 05, 20252025 (Q1)-2.54-1.92-1.45-32.06% (-0.47)
Mar 10, 20252024 (Q4)0.501.202.11-43.16% (-0.91)
Nov 04, 20242024 (Q3)-1.740.900.7420.90% (+0.16)

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