BNTX

Prezzo BioNTech

BNTX
$102,06
-$0,05(-0,04%)

*Data last updated: 2026-04-28 23:28 (UTC+8)

As of 2026-04-28 23:28, BioNTech (BNTX) is priced at $102,06, with a total market cap of $25,65B, a P/E ratio of -17,94, and a dividend yield of 0,00%. Today, the stock price fluctuated between $100,69 and $102,25. The current price is 1,36% above the day's low and 0,18% below the day's high, with a trading volume of 516,83K. Over the past 52 weeks, BNTX has traded between $79,50 to $124,00, and the current price is -17,69% away from the 52-week high.

BNTX Key Stats

Yesterday's Close$102,06
Market Cap$25,65B
Volume516,83K
P/E Ratio-17,94
Dividend Yield (TTM)0,00%
Dividend Amount$2,11
Diluted EPS (TTM)4,63
Net Income (FY)-$1,09B
Revenue (FY)$2,75B
Earnings Date2026-05-05
EPS Estimate2,52
Revenue Estimate$210,15M
Shares Outstanding251,32M
Beta (1Y)1.593
Ex-Dividend Date2022-06-02
Dividend Payment Date2022-06-17

About BNTX

BioNTech SE, a biotechnology company, develops and commercializes immunotherapies for cancer and other infectious diseases. The company is developing FixVac product candidates, including BNT111, which is in Phase II clinical trial for advance melanoma; BNT112 that is in Phase I/IIa clinical trial for prostate cancer; BNT113, which is in Phase II clinical trial to treat HPV+ head and neck cancers; BNT114 that is in Phase I clinical trial for triple negative breast cancer; BNT115, which is in Phase I clinical trial in ovarian cancer; and BNT116, a preclinical stage product for non-small cell lung cancer. It also develops neoantigen specific immunotherapies, such as Autogene cevumeran (BNT122), which is in Phase II clinical trial for first-line melanoma, as well as in Phase 1a/1b clinical trial to treat multiple solid tumors; mRNA intratumoral immunotherapy comprising SAR441000 that is in Phase I clinical trial for solid tumors; and BNT141 and BNT142 that are in Phase I clinical trial to treat multiple solid tumors. In addition, the company develops RiboCytokines, which include BNT151, BNT152, and BNT153 to treat solid tumors; chimeric antigen receptor T cell immunotherapies, such as BNT211 to treat multiple solid tumors, and BNT221 for other cancers; and checkpoint immunomodulators consisting of GEN1046 and GEN1042, which are in Phase I/II clinical trial to treat solid tumors. Further, it develops BNT321, an IgG1 monoclonal antibody in Phase II clinical trial for pancreatic cancer; BNT411, a small molecule immunomodulator product candidate for solid tumors; prophylactic vaccine for COVID-19 and Influenza; and infectious disease immunotherapies and rare disease protein replacement therapies. The company has collaborations with Genentech, Inc.; Sanofi S.A.; Genmab A/S; Pfizer Inc.; Shanghai Fosun Pharmaceutical (Group) Co., Ltd.; and Regeneron Pharmaceuticals, Inc. BioNTech SE was incorporated in 2008 and is headquartered in Mainz, Germany.
SectorHealthcare
IndustryBiotechnology
CEOUgur Sahin
HeadquartersMainz,None,DE
Official Websitehttps://www.biontech.de
Employees (FY)7,80K
Average Revenue (1Y)$353,09K
Net Income per Employee-$139,77K

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BioNTech (BNTX) is currently trading at $102,06, with a 24h change of -0,04%. The 52-week trading range is $79,50–$124,00.

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04-26 19:45
Moderna stock surges as FDA reverses course, agrees to review new flu shot ========================================================================== Jake Conley · Breaking Business News Reporter Thu, February 19, 2026 at 1:20 AM GMT+9 2 min read In this article: * StockStory Top Pick MRK -0.75% * MRNA +5.67% PFE -0.05% BNTX +1.40% AZN +0.30% Moderna (MRNA) stock jumped more than 6% on Wednesday after the US Food and Drug Administration agreed to review the drugmaker's first flu shot of the season, reversing course on a decision to reject the review last week. Moderna recently developed a new flu vaccine using the same mRNA technique that underpins its COVID-19 vaccine. But after requesting review from the federal government, the FDA initially declined to review the drug — a necessary regulatory step toward bringing the drug to market — saying that it wasn't satisfied with Moderna's trials. Shares fell roughly 2% on Feb. 10 after Moderna published the FDA's "refusal-to-file" letter. On the company's fourth quarter earnings call, CEO Stéphane Bancel said current "uncertainty" in the US regulatory regime "creates real challenges for businesses, patients and the broader innovation ecosystem." On Wednesday morning, however, Moderna announced in a press release that the FDA had reversed course and agreed to review the drug. NasdaqGS - Nasdaq Real Time Price • USD (MRNA) ======= 追蹤 View Quote Details 46.42 +2.49 (+5.67%) As of 11:45:49 AM EST. Market Open. Advanced Chart The drugmaker said that, to expedite approval, it had proposed a "regulatory pathway based on age, seeking full approval for adults 50 to 64 years of age and accelerated approval for adults 65 and older." "We appreciate the FDA's engagement in a constructive Type A meeting and its agreement to advance our application for review," Bancel said in the statement. "Pending FDA approval, we look forward to making our flu vaccine available later this year so that America's seniors have access to a new option to protect themselves against flu." The gains add to a soaring start to 2026 for Moderna, whose shares are up more than 55% since the start of the year, even as pharmaceutical competitors like Pfizer, BioNTech, and AstraZeneca have seen much smaller gains. Shares rallied earlier in February when Moderna reported a smaller-than-expected loss in adjusted earnings per share (EPS). The drugmaker reported an adjusted loss of $2.11 per share and revenue of $678 million against analysts' estimates of a loss of $2.64 per share and $623.9 million. At the same time, Moderna's performance has been bolstered by positive developments in its drug development pipeline. Shares surged by roughly 15% on Jan. 21 after the company announced positive clinical results on an experimental skin cancer vaccine developed in partnership with Merck (MRK). The company also announced in February a five-year strategic agreement with the government of Mexico to supply respiratory vaccines in the country. 繼續閱讀 Moderna CEO Stéphane Bancel (pictured above) said on the company's most recent earnings call that uncertainty in the US regulatory regime "creates real challenges for businesses, patients and the broader innovation ecosystem." (Eugene Gologursky/Getty Images for Fast Company) · Eugene Gologursky via Getty Images _Jake Conley is a breaking news reporter covering US equities for Yahoo Finance. Follow him on X at @byjakeconley or email him at __jake.co__nley@yahooinc.com_. **Click here for the latest stock market news and in-depth analysis, including events that move stocks** **Read the latest financial and business news from Yahoo Finance** 條款 及 私隱政策 Privacy Dashboard More Info
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