BNTX
NASDAQBioNTech SE
Website
News25/Ratings12
News · 26 weeks57-65%
2025-10-262026-04-19
Mix3490d
- Insider15(44%)
- SEC Filings7(21%)
- Other7(21%)
- Earnings3(9%)
- Leadership1(3%)
- Analyst1(3%)
Latest news
25 items- INSIDERChief Operating Officer Poetting Sierk sold $5,527,960 worth of Ordinary Shares (50,000 units at $110.56) (SEC Form 4)4 - BioNTech SE (0001776985) (Issuer)
- PRBioNTech to Report First Quarter 2026 Financial Results and Corporate Update on May 5, 2026MAINZ, Germany, April 21, 2026 (GLOBE NEWSWIRE) -- BioNTech SE (NASDAQ:BNTX, "BioNTech" or "the Company")) will announce its financial results for the first quarter 2026 on Tuesday, May 5, 2026. Additionally, the Company will host a conference call and webcast that day at 8:00 a.m. ET (2:00 p.m. CET) for investors, financial analysts and the general public to discuss its financial results and provide a corporate update.To access the live conference call via telephone, please register via this link. Once registered, dial-in numbers and a PIN will be provided. It is recommended to register at least one day in advance. The slide presentation and audio of the webcast will be available via this l
- INSIDERAmendment: SEC Form 3 filed by new insider Sahin Ugur3/A - BioNTech SE (0001776985) (Issuer)
- SECSEC Form 6-K filed by BioNTech SE6-K - BioNTech SE (0001776985) (Filer)
- PRBioNTech and DualityBio's Antibody-Drug Conjugate Trastuzumab Pamirtecan Demonstrated Clinically Meaningful Efficacy in Patients with HER2-Expressing, Recurrent Endometrial CancerTrastuzumab pamirtecan, an investigational HER2-targeted antibody-drug conjugate, met the primary efficacy endpoint in a Phase 2 cohort of heavily pre-treated patients with HER2-expressing, recurrent endometrial cancer, an area of high unmet medical needData demonstrated clinically meaningful antitumor activity across all HER2 expression levels and a manageable safety profile, with centrallyi HER2-tested patients showing a confirmed objective response rate of 47.9% in all evaluable patients, 49.3% in patients with prior immune checkpoint inhibitor treatment, and a median progression-free survival of 8.1 monthsLargest trial to date to report results for a HER2-targeted antibody-drug conjugate
- SECSEC Form 6-K filed by BioNTech SE6-K - BioNTech SE (0001776985) (Filer)
- SECAmendment: SEC Form 20-F/A filed by BioNTech SE20-F/A - BioNTech SE (0001776985) (Filer)
- INSIDERSEC Form 3 filed by new insider Blackwood Nicola Claire3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Morawietz Anja3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Staudigl Rudolf3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Sahin Ugur3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Zapata Gomez Ramon3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Ryan James Timothy Patrick3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Jimenez Kylie3 - BioNTech SE (0001776985) (Issuer)
- SECSEC Form 6-K filed by BioNTech SE6-K - BioNTech SE (0001776985) (Filer)
- PRBioNTech Clinical Data at ELCC 2026 Highlight Potential of Differentiated Late-Stage Portfolio in Lung CancerPresentations showcase progress in BioNTech's late-stage lung cancer programs, reinforcing the potential of the Company's differentiated portfolio spanning immunomodulators, antibody-drug conjugates, mRNA cancer immunotherapies, and their combinationsData updates for pumitamig, a PD-L1xVEGF-A bispecific immunomodulator, from three clinical trials conducted in China further strengthen the evidence supporting its previously observed efficacy and safety profile in lung cancerResults of stage 1 from the global Phase 3 PRESERVE-003 clinical trial of gotistobart showed clinically meaningful survival outcomes and antitumor activity compared to the current standard of care in second-line or later th
- INSIDERSEC Form 3 filed by new insider Jeggle Helmut Wolfgang3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Poetting Sierk3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Motschmann Michael3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Wandschneider Ulrich3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Tureci Ozlem3 - BioNTech SE (0001776985) (Issuer)
- INSIDERSEC Form 3 filed by new insider Hanekamp Annemarie3 - BioNTech SE (0001776985) (Issuer)
- SECSEC Form 20-F filed by BioNTech SE20-F - BioNTech SE (0001776985) (Filer)
- SECSEC Form 6-K filed by BioNTech SE6-K - BioNTech SE (0001776985) (Filer)
- PRBioNTech Announces Fourth Quarter and Full Year 2025 Financial Results and Corporate UpdateBioNTech on track for a catalyst-rich year with six late-stage data readouts expected across immunomodulators, antibody-drug conjugates and mRNA cancer immunotherapies Increased focus on PD-L11/VEGF-A bispecific immunomodulator pumitamig with eight global Phase 3 clinical trials planned to be ongoing for year-end in collaboration with Bristol Myers Squibb Full year 2025 revenues of €2.9 billion2, net loss of €1.1 billion (adjusted3 net loss of €0.1 billion) and diluted loss per share of €4.70 ($5.314) (adjusted3 diluted loss per share of €0.48 ($0.554)) Strong financial position continues to de-risk execution with cash, cash equivalents and security investments of €17.2 billion5Expect 202